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enzyme (lysozyme)

 
Enzymes
  Enzyme classes:
  EC 1: Oxidoreductases
  EC 2: Transferases
  EC 3: Hydrolases
  EC 4: Lyases
  EC 5: Isomerases
    EC 5.1
    EC 5.2
      EC 5.2.1
        EC 5.2.1.1
        EC 5.2.1.2
        EC 5.2.1.3
        EC 5.2.1.4
        EC 5.2.1.5
        EC 5.2.1.6
        EC 5.2.1.7
        EC 5.2.1.8
        EC 5.2.1.9
        EC 5.2.1.10
        EC 5.2.1.11
    EC 5.3
    EC 5.4
    EC 5.5
    EC 5.99
  EC 6: Ligases
  General information:
  Catalytic mechanism
  Enzyme kinetics
  Inhibitors
  Enzymes in industry

EC 5.2.1.8 - peptidylproline cis- trans- isomerase (peptidylprolyl isomerase)



3D structures of EC 5.2.1.8 - peptidylprolyl isomerase in Protein Data Bank

updated: 27 October 2021, 5:15

In total: 662 PDB structures of EC 5.2.1.8 - peptidylprolyl isomerase:
  1. 1a33: Peptidylprolyl Isomerase, Cyclophilin-like Domain from Brugia Malayi
  2. 1a7x: Fkbp12-fk1012 Complex
  3. 1ak4: Human Cyclophilin a Bound to The Amino-terminal Domain of Hiv-1 Capsid
  4. 1awq: Cypa Complexed with Hagpia (pseudo-symmetric Monomer)
  5. 1awr: Cypa Complexed with Hagpia
  6. 1aws: Secypa Complexed with Hagpia (pseudo-symmetric Monomer)
  7. 1awt: Secypa Complexed with Hagpia
  8. 1awu: Cypa Complexed with Hvgpia (pseudo-symmetric Monomer)
  9. 1awv: Cypa Complexed with Hvgpia
  10. 1b6c: Crystal Structure of The Cytoplasmic Domain of The Type I Tgf-beta Receptor in Complex with Fkbp12
  11. 1bck: Human Cyclophilin a Complexed with 2-thr Cyclosporin
  12. 6i42: Structure of The Alpha-synuclein Prenac/cyclophilin A-complex
  13. 1bkf: Fk506 Binding Protein Fkbp Mutant R42K/H87V Complex with Immunosuppressant Fk506
  14. 1bl4: Fkbp Mutant F36V Complexed with Remodeled Synthetic Ligand
  15. 1c5f: Crystal Structure of The Cyclophilin-like Domain from Brugia Malayi Complexed with Cyclosporin a
  16. 1cwa: X-ray Structure of a Monomeric Cyclophilin A-cyclosporin a Crystal Complex at 2.1 Angstroms Resolution
  17. 1cwb: The X-ray Structure of (MEBM2T)1-CYCLOSPORIN Complexed with Cyclophilin a Provides an Explanation for Its Anomalously High Immunosuppressive Activity
  18. 1cwc: Improved Binding Affinity for Cyclophilin a by a Cyclosporin Derivative Singly Modified at Its Effector Domain
  19. 1cwf: Human Cyclophilin a Complexed with 2-val Cyclosporin
  20. 1cwh: Human Cyclophilin a Complexed with 3-d-ser Cyclosporin
  21. 1cwi: Human Cyclophilin a Complexed with 2-val 3-(n-methyl)-d- Alanine Cyclosporin
  22. 1cwj: Human Cyclophilin a Complexed with 2-val 3-s-methyl- Sarcosine Cyclosporin
  23. 1cwk: Human Cyclophilin a Complexed with 1-(6,7-dihydro)mebmt 2- Val 3-d-(2-s-methyl)sarcosine Cyclosporin
  24. 1cwl: Human Cyclophilin a Complexed with 4 4-hydroxy-meleu Cyclosporin
  25. 1cwm: Human Cyclophilin a Complexed with 4 Meile Cyclosporin
  26. 1cwo: Human Cyclophilin a Complexed with Thr2, Leu5, D-hiv8, Leu10 Cyclosporin
  27. 1cyn: Cyclophilin B Complexed with [d-(cholinylester)ser8]- Cyclosporin
  28. 1d6o: Native Fkbp
  29. 1d7h: Fkbp Complexed with Dmso
  30. 1d7i: Fkbp Complexed with Methyl Methylsulfinylmethyl Sulfide (dss)
  31. 1d7j: Fkbp Complexed with 4-hydroxy-2-butanone
  32. 1dyw: Biochemical and Structural Characterization of a Divergent Loop Cyclophilin from Caenorhabditis Elegans
  33. 1e8k: Cyclophilin 3 Complexed with Dipeptide Ala-pro
  34. 1eym: Fk506 Binding Protein Mutant, Homodimeric Complex
  35. 1f8a: Structural Basis for The Phosphoserine-proline Recognition by Group IV Ww Domains
  36. 1fap: The Structure of The Immunophilin-immunosuppressant Fkbp12- Rapamycin Complex Interacting with Human Frap
  37. 1fd9: Crystal Structure of The Macrophage Infectivity Potentiator Protein (mip) a Major Virulence Factor from Legionella Pneumophila
  38. 1fgl: Cyclophilin a Complexed with a Fragment of Hiv-1 Gag Protein
  39. 1fkj: Atomic Structure of Fkbp12-fk506, an Immunophilin Immunosuppressant Complex
  40. 1fkk: Atomic Structure of Fkbp12, an Immunophilin Binding Protein
  41. 1fkl: Atomic Structure of Fkbp12-rapaymycin, an Immunophilin- Immunosuppressant Complex
  42. 1h0p: Cyclophilin_5 from C. Elegans
  43. 1i6c: Solution Structure of Pin1 Ww Domain
  44. 1i8g: Solution Structure of Pin1 Ww Domain Complexed with Cdc25 Phosphothreonine Peptide
  45. 1i8h: Solution Structure of Pin1 Ww Domain Complexed with Human Tau Phosphothreonine Peptide
  46. 1ihg: Bovine Cyclophilin 40, Monoclinic Form
  47. 1iip: Bovine Cyclophilin 40, Tetragonal Form
  48. 1ist: Crystal Structure of Yeast Cyclophilin A, Cpr1
  49. 1ix5: Solution Structure of The Methanococcus Thermolithotrophicus Fkbp
  50. 1j2a: Structure of E. Coli Cyclophilin B K163T Mutant
  51. 1j4h: Crystal Structure Analysis of The Fkbp12 Complexed with 000107 Small Molecule
  52. 1j4i: Crystal Structure Analysis of The Fkbp12 Complexed with 000308 Small Molecule
  53. 1j4r: Fk506 Binding Protein Complexed with Fkb-001
  54. 1jns: Nmr Structure of The E. Coli Peptidyl-prolyl Cis/trans- Isomerase Parvulin 10
  55. 1jnt: Nmr Structure of The E. Coli Peptidyl-prolyl Cis/trans- Isomerase Parvulin 10
  56. 1jvw: Trypanosoma Cruzi Macrophage Infectivity Potentiator (tcmip)
  57. 4fap: Atomic Structures of The Rapamycin Analogs in Complex with Both Human Fkbp12 and Frb Domain of Frap
  58. 4cyh: Cyclophilin a Complexed with Dipeptide His-pro
  59. 1kt0: Structure of The Large Fkbp-like Protein, Fkbp51, Involved in Steroid Receptor Complexes
  60. 1kt1: Structure of The Large Fkbp-like Protein, Fkbp51, Involved in Steroid Receptor Complexes
  61. 1l1p: Solution Structure of The Ppiase Domain from E. Coli Trigger Factor
  62. 3odk: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  63. 1lop: Cyclophilin a Complexed with Succinyl-ala-pro-ala-p- Nitroanilide
  64. 1m5y: Crystallographic Structure of Sura, a Molecular Chaperone That Facilitates Outer Membrane Porin Folding
  65. 1m63: Crystal Structure of Calcineurin-cyclophilin-cyclosporin Shows Common but Distinct Recognition of Immunophilin-drug Complexes
  66. 1m9c: X-ray Crystal Structure of Cyclophilin A/hiv-1 Ca N- Terminal Domain (1-146) M-type Complex.
  67. 1m9d: X-ray Crystal Structure of Cyclophilin A/hiv-1 Ca N- Terminal Domain (1-146) O-type Chimera Complex.
  68. 1m9e: X-ray Crystal Structure of Cyclophilin A/hiv-1 Ca N- Terminal Domain (1-146) M-type H87A Complex.
  69. 1m9f: X-ray Crystal Structure of Cyclophilin A/hiv-1 Ca N- Terminal Domain (1-146) M-type H87A,A88M Complex.
  70. 1m9x: X-ray Crystal Structure of Cyclophilin A/hiv-1 Ca N- Terminal Domain (1-146) M-type H87A,A88M,G89A Complex.
  71. 1m9y: X-ray Crystal Structure of Cyclophilin A/hiv-1 Ca N- Terminal Domain (1-146) M-type H87A,G89A Complex.
  72. 1mf8: Crystal Structure of Human Calcineurin Complexed with Cyclosporin a and Human Cyclophilin
  73. 1mik: The Role of Water Molecules in The Structure-based Design of (5-hydroxynorvaline)-2-cyclosporin: Synthesis, Biological Activity, and Crystallographic Analysis with Cyclophilin a
  74. 3mdy: Crystal Structure of The Cytoplasmic Domain of The Bone Morphogenetic Protein Receptor Type-1b (BMPR1B) in Complex with Fkbp12 and Ldn- 193189
  75. 3mdf: Crystal Structure of The Rrm Domain of Cyclophilin 33
  76. 1n1a: Crystal Structure of The N-terminal Domain of Human Fkbp52
  77. 3luo: Crystal Structure and Functional Characterization of The Thermophilic Prolyl Isomerase and Chaperone Slyd
  78. 3lpy: Crystal Structure of The Rrm Domain of Cyp33
  79. 1nmk: The Sanglifehrin-cyclophilin Interaction: Degradation Work, Synthetic Macrocyclic Analogues, X-ray Crystal Structure and Binding Data
  80. 1nmv: Solution Structure of Human Pin1
  81. 1nmw: Solution Structure of The Ppiase Domain of Human Pin1
  82. 1nsg: The Structure of The Immunophilin-immunosuppressant Fkbp12- Rapamycin Complex Interacting with Human Frap
  83. 1oca: Human Cyclophilin A, Unligated, Nmr, 20 Structures
  84. 3kce: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  85. 3kai: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  86. 3kah: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  87. 3kag: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  88. 3kaf: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  89. 3kad: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  90. 3kac: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  91. 1oms: Structure Determination by Mad: E.coli Trigger Factor Binding at The Ribosomal Exit Tunnel.
  92. 3kab: Structure-guided Design of Alpha-amino Acid-derived Pin1 Inhibitors
  93. 3k2c: Crystal Structure of Peptidyl-prolyl Cis-trans Isomerase from Encephalitozoon Cuniculi at 1.9 a Resolution
  94. 3k0r: Cryogenic Structure of Cypa Mutant ARG55LYS
  95. 3k0q: Cryogenic Structure of Cypa Mutant SER99THR (2)
  96. 3k0p: Cryogenic Structure of Cypa Mutant SER99THR
  97. 3k0o: Room Temperature Structure of Cypa Mutant SER99THR
  98. 3k0n: Room Temperature Structure of Cypa
  99. 3k0m: Cryogenic Structure of Cypa
  100. 3jyj: Structure-based Design of Novel Pin1 Inhibitors (ii)
  101. 3jxv: Crystal Structure of The 3 Fkbp Domains of Wheat Fkbp73
  102. 1p5q: Crystal Structure of Fkbp52 C-terminal Domain
  103. 1p9y: Ribosome Binding of E. Coli Trigger Factor Mutant F44L.
  104. 1pin: Pin1 Peptidyl-prolyl Cis-trans Isomerase from Homo Sapiens
  105. 3ikg: Structure-based Design of Novel Pin1 Inhibitors (i)
  106. 3ikd: Structure-based Design of Novel Pin1 Inhibitors (i)
  107. 3ik8: Structure-based Design of Novel Pin1 Inhibitors (i)
  108. 3ici: Crystal Structure of Cyclophilin B in Complex with Calmegin Fragment
  109. 3ich: Crystal Structure of Cyclophilin B at 1.2 a Resolution
  110. 6o49: Crystal Structure of Smt Fusion Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with Sf339
  111. 3i6c: Structure-based Design of Novel Pin1 Inhibitors (ii)
  112. 1q1c: Crystal Structure of N(1-260) of Human Fkbp52
  113. 1q6h: Crystal Structure of a Truncated Form of Fkpa from Escherichia Coli
  114. 1q6i: Crystal Structure of a Truncated Form of Fkpa from Escherichia Coli, in Complex with Immunosuppressant Fk506
  115. 1q6u: Crystal Structure of Fkpa from Escherichia Coli
  116. 1qng: Plasmodium Falciparum Cyclophilin Complexed with Cyclosporin a
  117. 1qnh: Plasmodium Falciparum Cyclophilin (double Mutant) Complexed with Cyclosporin a
  118. 3h9r: Crystal Structure of The Kinase Domain of Type I Activin Receptor (acvr1) in Complex with Fkbp12 and Dorsomorphin
  119. 1qz2: Crystal Structure of Fkbp52 C-terminal Domain Complex with The C-terminal Peptide Meevd of Hsp90
  120. 3gpk: Crystal Structure of Ppic-type Peptidyl-prolyl Cis-trans Isomerase Domain at 1.55a Resolution.
  121. 3fap: Atomic Structures of The Rapamycin Analogs in Complex with Both Human Fkbp12 and Frb Domain of Frap
  122. 3ey6: Crystal Structure of The Fk506-binding Domain of Human Fkbp38
  123. 3eov: Crystal Structure of Cyclophilin from Leishmania Donovani Ligated with Cyclosporin a
  124. 1tco: Ternary Complex of a Calcineurin a Fragment, Calcineurin B, Fkbp12 and The Immunosuppressant Drug Fk506 (tacrolimus)
  125. 1u79: Crystal Structure of Atfkbp13
  126. 3cys: Determination of The Nmr Solution Structure of The Cyclophilin A-cyclosporin a Complex
  127. 3cyh: Cyclophilin a Complexed with Dipeptide Ser-pro
  128. 3cgn: Crystal Structure of Thermophilic Slyd
  129. 3cgm: Crystal Structure of Thermophilic Slyd
  130. 1v9t: Structure of E. Coli Cyclophilin B K163T Mutant Bound to Succinyl-ala-pro-ala-p-nitroanilide
  131. 1vai: Structure of E. Coli Cyclophilin B K163T Mutant Bound to N- Acetyl-ala-ala-pro-ala-7-amino-4-methylcoumarin
  132. 1vdn: Crystal Structure of Yeast Cyclophilin a Complexed with Ace- Ala-ala-pro-ala-7-amino-4-methylcoumarin
  133. 6o4a: Crystal Structure of Smt Fusion Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with Sf355
  134. 6u5e: Rt Xfel Structure of Cypa Solved Using Celloluse Carrier Media
  135. 6u5g: Microed Structure of a Fib-milled Cypa Crystal
  136. 3bt8: Crystal Structure of Mutant Cyclophilin (R147A) from Leishmania Donovani
  137. 1w74: X-ray Structure of Peptidyl-prolyl Cis-trans Isomerase A, Ppia, Rv0009, from Mycobacterium Tuberculosis.
  138. 1w8l: Enzymatic and Structural Characterization of Non Peptide Ligand Cyclophilin Complexes
  139. 1w8m: Enzymatic and Structural Characterisation of Non Peptide Ligand Cyclophilin Complexes
  140. 1w8v: Enzymatic and Structural Characterization of Non Peptide Ligand Cyclophilin Complexes
  141. 3b7x: Crystal Structure of Human Fk506-binding Protein 6
  142. 2zr6: Crystal Structure of a Mutant Pin1 Peptidyl-prolyl Cis-trans Isomerase
  143. 2zr5: Crystal Structure of a Mutant Pin1 Peptidyl-prolyl Cis-trans Isomerase
  144. 2zr4: Crystal Structure of a Mutant Pin1 Peptidyl-prolyl Cis-trans Isomerase
  145. 2zqv: Crystal Structure of a Mutant Pin1 Peptidyl-prolyl Cis-trans Isomerase
  146. 2zqu: Crystal Structure of a Mutant Pin1 Peptidyl-prolyl Cis-trans Isomerase
  147. 2zqt: Crystal Structure of a Mutant Pin1 Peptidyl-prolyl Cis-trans Isomerase
  148. 2zqs: Crystal Structure of a Mutant Pin1 Peptidyl-prolyl Cis-trans Isomerase
  149. 2z6w: Crystal Structure of Human Cyclophilin D in Complex with Cyclosporin a
  150. 1xq7: Cyclophilin from Trypanosoma Cruzi Bound to Cyclosporin a
  151. 2xgy: Complex of Rabbit Endogenous Lentivirus (relik)capsid with Cyclophilin a
  152. 1xwn: Solution Structure of Cyclophilin like 1(ppil1) and Insights into Its Interaction with Skip
  153. 1xyh: Crystal Structure of Recombinant Human Cyclophilin J
  154. 2x7k: The Crystal Structure of Ppil1 in Complex with Cyclosporine a Suggests a Binding Mode for Skip
  155. 1y0o: Crystal Structure of Reduced Atfkbp13
  156. 2x2d: Acetyl-cypa:hiv-1 N-term Capsid Domain Complex
  157. 2x2c: Acetyl-cypa:cyclosporine Complex
  158. 2x2a: Free Acetyl-cypa Trigonal Form
  159. 2x25: Free Acetyl-cypa Orthorhombic Form
  160. 1ynd: Structure of Human Cyclophilin a in Complex with The Novel Immunosuppressant Sanglifehrin a at 1.6a Resolution
  161. 2wlw: Structure of The N-terminal Capsid Domain of Hiv-2
  162. 1yw5: Peptidyl-prolyl Isomerase Ess1 from Candida Albicans
  163. 2wfj: Atomic Resolution Crystal Structure of The Ppiase Domain of Human Cyclophilin G in Complex with Cyclosporin A.
  164. 2wfi: Atomic Resolution Crystal Structure of The Ppiase Domain of Human Cyclophilin G
  165. 6u5c: Rt Xfel Structure of Cypa Solved Using Mesh Injection System
  166. 6u5d: Rt Xfel Structure of Cypa Solved Using Lcp Injection System
  167. 1z81: Crystal Structure of Cyclophilin from Plasmodium Yoelii.
  168. 1zcn: Human Pin1 Ng Mutant
  169. 1zk6: Nmr Solution Structure of B. Subtilis Prsa Ppiase
  170. 1zkc: Crystal Structure of The Cyclophiln_ring Domain of Human Peptidylprolyl Isomerase (cyclophilin)-like 2 Isoform B
  171. 1zkf: Cyrstal Structure of Human Cyclophilin-a in Complex with Suc-agpf-pna
  172. 1zmf: C Domain of Human Cyclophilin-33(hcyp33)
  173. 2vn1: Crystal Structure of The Fk506-binding Domain of Plasmodium Falciparum Fkbp35 in Complex with Fk506
  174. 7jtk: Radial Spoke 1 Isolated from Chlamydomonas Reinhardtii
  175. 6vrx: Mucor Circinelloides Fkbp12 Protein Bound with Fk506 in P3221 Space Group
  176. 6vcv: Aspergillus Fumigatus Fkbp12 Protein Bound with Apx879 in P1 Space Group
  177. 6vcu: Homo Sapiens Fkbp12 Protein Bound with Apx879 in P32 Space Group
  178. 6vct: Mucor Circinelloides Fkbp12 Protein Bound with Apx879 in C2221 Space Group
  179. 6lkb: Crystal Structure of The Peptidylprolyl Isomerase Domain of Arabidopsis Thaliana Cyp71.
  180. 2a2n: Crystal Structure of The Peptidylprolyl Isomerase Domain of Human Ppwd1
  181. 2vcd: Solution Structure of The Fkbp-domain of Legionella Pneumophila Mip in Complex with Rapamycin
  182. 7a5p: Human C Complex Spliceosome - Medium-resolution Periphery
  183. 2alf: Crystal Structure of Human Cypa Mutant K131A
  184. 6zym: Human C Complex Spliceosome - High-resolution Core
  185. 2uz5: Solution Structure of The Fkbp-domain of Legionella Pneumophila Mip
  186. 2rqs: 3d Structure of Pin from The Psychrophilic Archeon Cenarcheaum Symbiosum (cspin)
  187. 2rmc: Crystal Structure of Murine Cyclophilin C Complexed with Immunosuppressive Drug Cyclosporin a
  188. 2rmb: Crystal Structures of Cyclophilin a Complexed with Cyclosporin a and N-methyl-4-[(e)-2-butenyl]-4,4- Dimethylthreonine Cyclosporin a
  189. 2rma: Crystal Structures of Cyclophilin a Complexed with Cyclosporin a and N-methyl-4-[(e)-2-butenyl]-4,4- Dimethylthreonine Cyclosporin a
  190. 2bit: Crystal Structure of Human Cyclophilin D at 1.7 a Resolution
  191. 2biu: Crystal Structure of Human Cyclophilin D at 1.7 a Resolution, Dmso Complex
  192. 2r99: Crystal Structure of Cyclophilin Abh-like Domain of Human Peptidylprolyl Isomerase E Isoform 1
  193. 2ck1: The Structure of Oxidised Cyclophilin a from S. Mansoni
  194. 2cmt: The Structure of Reduced Cyclophilin a from S. Mansoni
  195. 6y3e: Scaffold-ligand Complex with Ligand Unmodelled
  196. 6zdj: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,10)
  197. 2q5a: Human Pin1 Bound to L-peptide
  198. 2cqb: Solution Structure of The Rna Recognition Motif in Peptidyl- Prolyl Cis-trans Isomerase E
  199. 2pv3: Crystallographic Structure of Sura Fragment Lacking The Second Peptidyl-prolyl Isomerase Domain Complexed with Peptide Nftlkfwdifrk
  200. 2pv2: Crystallographic Structure of Sura First Peptidyl-prolyl Isomerase Domain Complexed with Peptide Nftlkfwdifrk
  201. 2pv1: Crystallographic Structure of Sura First Peptidyl-prolyl Isomerase Domain Complexed with Peptide Weyipnv
  202. 2cyh: Cyclophilin a Complexed with Dipeptide Ala-pro
  203. 2ppp: Crystal Structure of E60Q Mutant of Fkbp12
  204. 2ppo: Crystal Structure of E60A Mutant of Fkbp12
  205. 2ppn: Crystal Structure of Fkbp12
  206. 2pbc: Fk506-binding Protein 2
  207. 2dg3: Wildtype Fk506-binding Protein Complexed with Rapamycin
  208. 2dg4: Fk506-binding Protein Mutant Wf59 Complexed with Rapamycin
  209. 2dg9: Fk506-binding Protein Mutant Wl59 Complexed with Rapamycin
  210. 2ose: Crystal Structure of The Mimivirus Cyclophilin
  211. 2ok3: X-ray Structure of Human Cyclophilin J at 2.0 Angstrom
  212. 2oju: X-ray Structure of Complex of Human Cyclophilin J with Cyclosporin a
  213. 6y9z: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,9)
  214. 6y9y: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-7,13)
  215. 6y9x: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,7)
  216. 6y9w: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,8)
  217. 6y9v: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-8,13)
  218. 2ofn: Solution Structure of Fk506-binding Domain (fkbd)of Fkbp35 from Plasmodium Falciparum
  219. 6bta: Cypa Mutant - S99T C115S
  220. 6bhf: Crystal Structure of The Petidylprolyl Cis,trans-isomerase from Helicobacter Pylori
  221. 2nul: Peptidylprolyl Isomerase from E. Coli
  222. 2l2s: Solution Structure of Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with 1-{[(4-methylphenyl) Thio]acetyl}piperidine
  223. 5zr0: Solution Structure of Peptidyl-prolyl Cis/trans Isomerase Domain of Trigger Factor in Complex with Mbp
  224. 2kyx: Solution Structure of The Rrm Domain of Cyp33
  225. 2esl: Human Cyclophilin C in Complex with Cyclosporin a
  226. 2f21: Human Pin1 Fip Mutant
  227. 2fap: The Structure of The Immunophilin-immunosuppressant Fkbp12- (c16)-ethoxy Rapamycin Complex Interacting with Huma
  228. 2fu0: Plasmodium Falciparum Cyclophilin PFE0505W Putative Cyclosporin-binding Domain
  229. 5z58: Cryo-em Structure of a Human Activated Spliceosome (early Bact) at 4.9 Angstrom.
  230. 2gw2: Crystal Structure of The Peptidyl-prolyl Isomerase Domain of Human Cyclophilin G
  231. 2haq: Crystal Structure of Cyclophilin a from Leishmania Donovani
  232. 2he9: Structure of The Peptidylprolyl Isomerase Domain of The Human Nk-tumour Recognition Protein
  233. 2hqj: Cyclophilin from Leishmania Major
  234. 2igv: Cyclophilin 3 Complexed with Dipeptide Ser-pro
  235. 2igw: Cyclophilin 3 Complexed with Dipeptide Gly-pro
  236. 2itk: Human Pin1 Bound to D-peptide
  237. 6xd8: Crystal Structure of Peptidylprolyl Isomerase (prsa) Fragment from Bacillus Anthracis
  238. 2jv4: Structure Characterisation of Pina Ww Domain and Comparison with Other Group IV Ww Domains, Pin1 and Ess1
  239. 2jzv: Solution Structure of S. Aureus Prsa-ppiase
  240. 2k7n: Solution Structure of The Ppil1 Bound to a Fragment of Skip
  241. 2k8i: Solution Structure of E.coli Slyd
  242. 2kbu: Nmr Solution Structure of Pin1 Ww Domain Mutant with Beta Turn Mimic at Position 12
  243. 2kcf: The Nmr Solution Structure of The Isolated Apo Pin1 Ww Domain
  244. 2ke0: Solution Structure of Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei
  245. 6svh: Protein Allostery of The Ww Domain at Atomic Resolution: Ffpspr Bound Structure
  246. 6sve: Protein Allostery of The Ww Domain at Atomic Resolution: PCDC25C Bound Structure
  247. 6svc: Protein Allostery of The Ww Domain at Atomic Resolution: Apo Structure
  248. 2kfv: Structure of The Amino-terminal Domain of Human Fk506- Binding Protein 3 / Northeast Structural Genomics Consortium Target HT99A
  249. 2kfw: Solution Structure of Full-length Slyd from E.coli
  250. 2kgj: Solution Structure of Parvulin Domain of Ppid from E.coli
  251. 6m4w: Crystal Structure of Mbp Fused Split Fkbp-frb T2098L Mutant in Complex with Rapamycin
  252. 6m4v: Crystal Structure of Mbp Fused Split Fkbp in Complex with Rapamycin
  253. 6m4u: Crystal Structure of Fkbp-frb T2098L Mutant in Complex with Rapamycin
  254. 2ko7: Solution Structure of Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with Cycloheximide-n-ethylethanoate
  255. 6lxr: Tvcyp2 in Apo Form 4
  256. 6lxq: Tvcyp2 in Apo Form 3
  257. 6lxp: Tvcyp2 in Apo Form 2
  258. 6lxo: Tvcyp2 in Apo Form 1
  259. 2kr7: Solution Structure of Helicobacter Pylori Slyd
  260. 6x4q: Human Cyclophilin a Bound to a Series of Acylcic and Macrocyclic Inhibitors: (2r,5s,11s,14s,18e)-14-cyclobutyl-2,11,17,17-tetramethyl- 15-oxa-3,9,12,26,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23, 27~]nonacosa-1(25),18,20(28),21,23,26-hexaene-4,10,13,16-tetrone (compound 33)
  261. 6x4p: Human Cyclophilin a Bound to a Series of Acylcic and Macrocyclic Inhibitors: (2r,5s,11s,14s,18e)-2,11,17,17-tetramethyl-14-(propan-2- Yl)-15-oxa-3,9,12,26,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23, 27~]nonacosa-1(25),18,20(28),21,23,26-hexaene-4,10,13,16-tetrone (compound 28)
  262. 6x4o: Human Cyclophilin a Bound to a Series of Acylcic and Macrocyclic Inhibitors: (2r,5s,11s,14s,18e)-2,11-dimethyl-14-(propan-2-yl)-3-oxa- 9,12,15,21,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23,27~]nonacosa- 1(26),18,20,22,24,27-hexaene-4,10,13,16-tetrone (compound 21)
  263. 6x4n: Human Cyclophilin a Bound to a Series of Acylcic and Macrocyclic Inhibitors: (2r,5s,11s,14s,18e)-2,11,17,17-tetramethyl-14-(propan-2- Yl)-3-oxa-9,12,15,26,29-pentaazatetracyclo[18.5.3.1~5,9~.0~23, 27~]nonacosa-1(25),18,20(28),21,23,26-hexaene-4,10,13,16-tetrone (compound 24)
  264. 6x4m: Human Cyclophilin a Bound to a Series of Acylcic and Macrocyclic Inhibitors: Tert-butyl [(2s)-1-{[(3s,17s)-2,16-dioxo-10,15-dioxa-1, 21-diazatricyclo[15.3.1.1~5,9~]docosa-5(22),6,8-trien-3-yl]amino}-3- Methyl-1-oxobutan-2-yl]carbamate (compound 3)
  265. 6x3y: Human Cyclophilin a Bound to a Series of Acylcic and Macrocyclic Inhibitors
  266. 6x3r: Human Cyclophilin a Bound to a Series of Acylcic and Macrocyclic Inhibitors
  267. 2xp3: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  268. 2xp4: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  269. 2xp5: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  270. 2xp6: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  271. 2xp7: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  272. 2xp8: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  273. 2xp9: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  274. 2xpa: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  275. 2xpb: Discovery of Cell-active Phenyl-imidazole Pin1 Inhibitors by Structure-guided Fragment Evolution
  276. 3kz7: C-terminal Domain of Murine Fkbp25 Rapamycin Complex
  277. 3odi: Crystal Structure of Cyclophilin a in Complex with Voclosporin E- Isa247
  278. 3odl: Crystal Structure of Cyclophilin a in Complex with Voclosporin Z- Isa247
  279. 3pr9: Structural Analysis of Protein Folding by The Methanococcus Jannaschii Chaperone Fkbp26
  280. 3pra: Structural Analysis of Protein Folding by The Methanococcus Jannaschii Chaperone Fkbp26
  281. 3prb: Structural Analysis of Protein Folding by The Methanococcus Jannaschii Chaperone Fkbp26
  282. 3prd: Structural Analysis of Protein Folding by The Methanococcus Jannaschii Chaperone Fkbp26
  283. 6txx: Crystal Structure of Human Fkbp51 Fk1 Domain A19T Mutant in Complex with Safit2
  284. 6tx9: Crystal Structure of Human Fkbp51 Fk1 Domain A19T Mutant in Complex with Hydantoin
  285. 6tx8: Crystal Structure of Human Fkbp51 Fk1 Domain A19T Mutant in Complex with Imidazole
  286. 6tx7: Crystal Structure of Human Fkbp51 Fk1 Domain A19T Mutant in Complex with 2-piperidone
  287. 6tx6: Crystal Structure of Human Fkbp51 Fk1 Domain A19T Mutant in Complex with Nicotinamide
  288. 6tx5: Crystal Structure of Human Fkbp51 Fk1 Domain A19T Mutant in Complex with 4-methylimidazole
  289. 6tx4: Crystal Structure of Human Fkbp51 Fk1 Domain A19T Mutant in Complex with 2-pyridone
  290. 6rcy: Crystal Structure of Fk1 Domain of Fkbp52 in Complex with a Bio- Inspired Hybrid Fluorescent Ligand
  291. 6oqa: Crystal Structure of Cep250 Bound to Fkbp12 in The Presence of Fk506- like Novel Natural Product
  292. 2y78: Crystal Structure of Bpss1823, a Mip-like Chaperone from Burkholderia Pseudomallei
  293. 6ybm: Scaffold-ligand Complex with Ligand Unmodelled.
  294. 2lb3: Structure of The Ww Domain of Pin1 in Complex with a Human Phosphorylated Smad3 Derived Peptide
  295. 6vsi: Crystal Structure of Fkbp12 of Candida Auris
  296. 3o5d: Crystal Structure of a Fragment of Fkbp51 Comprising The Fk1 and Fk2 Domains
  297. 3o5e: Fk1 Domain of Fkbp51, Crystal Form VI
  298. 3o5f: Fk1 Domain of Fkbp51, Crystal Form VII
  299. 3o5g: Fk1 Domain of Fkbp51, Crystal Form I
  300. 3o5i: Fk1 Domain of Fkbp51, Crystal Form II
  301. 3o5j: Fk1 Domain of Fkbp51, Crystal Form III
  302. 3o5k: Fk1 Domain of Fkbp51, Crystal Form VIII
  303. 3o5l: Fk1 Domain Mutant A19T of Fkbp51, Crystal Form I
  304. 3o5m: Fk1 Domain Mutant A19T of Fkbp51, Crystal Form II
  305. 3o5o: Fk1 Domain Mutant A19T of Fkbp51, Crystal Form III
  306. 3o5p: Fk1 Domain Mutant A19T of Fkbp51, Crystal Form IV
  307. 3o5q: Fk1 Domain Mutant A19T of Fkbp51, Crystal Form Iv, in Presence of Dmso
  308. 3o5r: Complex of Fk506 with The Fk1 Domain Mutant A19T of Fkbp51
  309. 3s6m: The Structure of a Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei
  310. 6saf: The Fk1 Domain of Fkbp51 in Complex with (s)-(r)-3-(3,4- Dimethoxyphenyl)-1-(3-(2-morpholinoethoxy)phenyl)propyl 1-((1r,4ar, 8ar)-4-oxodecahydronaphthalene-1-carbonyl)piperidine-2-carboxylate
  311. 3oob: Structural and Functional Insights of Directly Targeting Pin1 by Epigallocatechin-3-gallate
  312. 3qyu: Crystal Structure of Human Cyclophilin D at 1.54 a Resolution at Room Temperature
  313. 3tc5: Selective Targeting of Disease-relevant Protein Binding Domains by O- Phosphorylated Natural Product Derivatives
  314. 2rs4: Nmr Strucure of Stereo-array Isotope Labelled (sail) Peptidyl-prolyl Cis-trans Isomerase from E. Coli (eppib)
  315. 6tz8: Crystal Structure of Cryptococcus Neoformans Calceineurin A, Calcineurin B, and Fkbp12 with Fk-506
  316. 6tz7: Crystal Structure of Aspergillus Fumigatus Calcineurin A, Calcineurin B, Fkbp12 and Fk506 (tacrolimus)
  317. 6tz6: Crystal Structure of Candida Albicans Calcineurin A, Calcineurin B, Fkbp12 and Fk506 (tacrolimus)
  318. 3uf8: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with Fk506
  319. 3uch: Crystal Structure of a Hypotherical Peptidyl-prolyl Cis-trans Isomerase E (ppie) from Homo Sapiens at 2.50 a Resolution
  320. 3pmp: Crystal Structure of Cyclophilin a from Moniliophthora Perniciosa in Complex with Cyclosporin a
  321. 6ra1: Human Cyclophilin D in Complex with Norbornane Fragment Derivative
  322. 6r9x: Human Cyclophilin D in Complex with N-cyclopentyl-n'-pyridin-2- Ylmethyl-oxalamide
  323. 6r9u: Human Cyclophilin D in Complex with Fragment
  324. 6r9s: Human Cyclophilin D in Complex with Bicyclic Fragment
  325. 6r8w: Human Cyclophilin D in Complex with 2-(exo-3,5-dioxo-4-aza- Tricyclo[5.2.1.02,6]dec-4-yl)-n-((1r,9r,10s)-10-hydroxy-12-oxa-8-aza- Tricyclo[7.3.1.02,7]trideca-2(7),3,5-trien-4-ylmethyl)-acetamide
  326. 6r8o: Human Cyclophilin D in Complex with 1-(((2r,3s,6r)-3-hydroxy-2,3,4,6- Tetrahydro-1h-2,6-methanobenzo[c][1,5]oxazocin-8-yl)methyl)-3-(2- ((r)-2-(2-(methylthio)phenyl)pyrrolidin-1-yl)-2-oxoethyl)urea
  327. 6r8l: Human Cyclophilin D in Complex with 1-((1s,9s,10s)-10-hydroxy-12-oxa- 8-aza-tricyclo[7.3.1.02,7]trideca-2,4,6-trien-4-ylmethyl)-3- {2-[(r)- 2-(2-methylsulfanyl-phenyl)-pyrrolidin-1-yl]-2-oxo-ethyl}-urea
  328. 6o33: Crystal Structure Analysis of Pin1
  329. 6o34: Crystal Structure Analysis of Pin1
  330. 3ui4: 0.8 a Resolution Crystal Structure of Human Parvulin 14
  331. 3ui5: Crystal Structure of Human Parvulin 14
  332. 3uqa: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation A54E from Burkholderia Pseudomallei Complexed with Fk506
  333. 3uqb: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation D44G from Burkholderia Pseudomallei Complexed with Fk506
  334. 3ntp: Human Pin1 Complexed with Reduced Amide Inhibitor
  335. 3vaw: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation V3I from Burkholderia Pseudomallei Complexed with Fk506
  336. 4dga: Trimcyp Cyclophilin Domain from Macaca Mulatta: Hiv-1 Ca(o-loop) Complex
  337. 4dgb: Trimcyp Cyclophilin Domain from Macaca Mulatta: Hiv-2 Ca Cyclophilin- Binding Loop Complex
  338. 4dgc: Trimcyp Cyclophilin Domain from Macaca Mulatta: Cyclosporin a Complex
  339. 4dgd: Trimcyp Cyclophilin Domain from Macaca Mulatta: H70C Mutant
  340. 4dge: Trimcyp Cyclophilin Domain from Macaca Mulatta: H70C Mutant, Hiv-1 Ca(o-loop) Complex
  341. 4dh0: X-ray Crystal Structure of 28-o-methylrapamycin Complexed with Fkbp12: Is The Cyclohexyl Moiety part of The Effector Domain of Rapamycin?
  342. 4dip: Crystal Structure of Human Peptidyl-prolyl Cis-trans Isomerase Fkbp14
  343. 3pa7: Crystal Structure of Fkbp from Plasmodium Vivax in Complex with Tetrapeptide Alpf
  344. 3t1u: Crystal Structure of The Complex of Cyclophilin-a Enzyme from Azotobacter Vinelandii with Sucafpfpna Peptide
  345. 3r49: Human Cyclophilin D Complexed with a Fragment
  346. 3r4g: Human Cyclophilin D Complexed with a Fragment
  347. 3r54: Human Cyclophilin D Complexed with a Fragment
  348. 3r56: Human Cyclophilin D Complexed with a Fragment
  349. 3r57: Human Cyclophilin D Complexed with a Fragment
  350. 3r59: Human Cyclophilin D Complexed with a Fragment
  351. 3rcf: Human Cyclophilin D Complexed with a Fragment
  352. 3rcg: Human Cyclophilin D Complexed with a Fragment
  353. 3rci: Human Cyclophilin D Complexed with a Fragment
  354. 3rck: Human Cyclophilin D Complexed with a Fragment
  355. 3rcl: Human Cyclophilin D Complexed with a Fragment
  356. 3rd9: Human Cyclophilin D Complexed with a Fragment
  357. 3rda: Human Cyclophilin D Complexed with a Fragment
  358. 3rdb: Human Cyclophilin D Complexed with a Fragment
  359. 3rdc: Human Cyclophilin D Complexed with an Inhibitor
  360. 3rdd: Human Cyclophilin a Complexed with an Inhibitor
  361. 4dz2: Crystal Structure of a Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation R92G from Burkholderia Pseudomallei Complexed with Fk506
  362. 4dz3: Crystal Structure of a Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation M61H from Burkholderia Pseudomallei Complexed with Fk506
  363. 3b09: Crystal Structure of The N-domain of Fkbp22 from Shewanella Sp. Sib1
  364. 4drq: Exploration of Pipecolate Sulfonamides as Binders of The Fk506-binding Proteins 51 and 52: Complex of Fkbp51 with 2-(3-((r)-1-((s)-1-(3,5- Dichlorophenylsulfonyl)piperidine-2-carbonyloxy)-3-(3,4-dimethoxy - Phenyl)propyl)phenoxy)acetic Acid
  365. 4drk: Evaluation of Synthetic Fk506 Analogs as Ligands for Fkbp51 and Fkbp52: Complex of Fkbp51 with {3-[(1r)-3-(3,4-dimethoxyphenyl)-1- ({[(2s)-1-(3,3-dimethyl-2-oxopentanoyl)piperidin-2-yl]carbonyl}oxy) Propyl]phenoxy}acetic Acid
  366. 4drm: Evaluation of Synthetic Fk506 Analogs as Ligands for Fkbp51 and Fkbp52: Complex of Fkbp51 with {3-[(1r)-3-(3,4-dimethoxyphenyl)-1- ({[(2s)-1-{[(1s,2r)-2-ethyl-1-hydroxycyclohexyl](oxo) Acetyl}piperidin-2-yl]carbonyl}oxy)propyl]phenoxy}acetic Acid
  367. 4drn: Evaluation of Synthetic Fk506 Analogs as Ligands for Fkbp51 and Fkbp52: Complex of Fkbp51 with {3-[(1r)-3-(3,4-dimethoxyphenyl)-1- ({[(2s)-1-{[(1s,2r)-2-ethyl-1-hydroxycyclohexyl](oxo) Acetyl}piperidin-2-yl]carbonyl}oxy)propyl]phenoxy}acetic Acid
  368. 4dro: Evaluation of Synthetic Fk506 Analogs as Ligands for Fkbp51 and Fkbp52: Complex of Fkbp51 with (1r)-3-(3,4-dimethoxyphenyl)-1- Phenylpropyl (2s)-1-{[(1r,2s)-2-ethyl-1-hydroxycyclohexyl](oxo) Acetyl}piperidine-2-carboxylate
  369. 4drp: Evaluation of Synthetic Fk506 Analogs as Ligands for The Fk506-binding Proteins 51 and 52: Complex of Fkbp51 with 2-(3-((r)-3-(3,4- Dimethoxyphenyl)-1-((s)-1-(2-((1r,2s)-2-ethyl-1-hydroxy-cyclohexyl)- 2-oxoacetyl)piperidine-2-carbonyloxy)propyl)phenoxy)acetic Acid from Cocrystallization
  370. 2rse: Nmr Structure of Fkbp12-mtor Frb Domain-rapamycin Complex Structure Determined Based on Pcs
  371. 3rfy: Crystal Structure of Arabidopsis Thaliana Cyclophilin 38 (atcyp38)
  372. 3tcz: Human Pin1 Bound to Cis Peptidomimetic Inhibitor
  373. 3tdb: Human Pin1 Bound to Trans Peptidomimetic Inhibitor
  374. 3uqi: Crystallographic Structure of Fkbp12 from Aedes Aegypti
  375. 4dt4: Crystal Structure of The Ppiase-chaperone Slpa with The Chaperone Binding Site Occupied by The Linker of The Purification Tag
  376. 6mke: Crystal Structure of Peptidylprolyl Isomerase from Naegleria Fowleri with Bound Fk506
  377. 6l2b: Crystal Structure of Cyclophilin Mutant I164M from Leishmania Donovani at 2.65 Angstrom Resolution
  378. 4fn2: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation D44G from Burkholderia Pseudomallei Complexed with Cj37
  379. 4g50: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation D44G from Burkholderia Pseudomallei Complexed with Cj168
  380. 4ggq: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with Cj40
  381. 2lj4: Solution Structure of The Tbpin1
  382. 6j45: Crystal Structure of E. Coli Peptide Deformylase Enzyme and Chaperone Trigger Factor Fitted into The Cryo-em Density Map of The Complex
  383. 6j2z: Atfkbp53 N-terminal Nucleoplasmin Domain
  384. 6j2m: Crystal Structure of Atfkbp53 C-terminal Domain
  385. 6j0a: Crystal Structure of E. Coli Methionine Aminopeptidase Enzyme and Chaperone Trigger Factor Fitted into The Cryo-em Density Map of The Complex
  386. 4giv: Crystal Structure of a Smt Fusion Peptidyl-prolyl Cis-trans Isomerase with Surface Mutation D44G from Burkholderia Pseudomallei Complexed with Cj183
  387. 6id1: Cryo-em Structure of a Human Intron Lariat Spliceosome after Prp43 Loaded (ils2 Complex) at 2.9 Angstrom Resolution
  388. 6id0: Cryo-em Structure of a Human Intron Lariat Spliceosome Prior to Prp43 Loaded (ils1 Complex) at 2.9 Angstrom Resolution
  389. 6icz: Cryo-em Structure of a Human Post-catalytic Spliceosome (p Complex) at 3.0 Angstrom
  390. 6i1s: Crystal Structure of The Acvr1 (alk2) Kinase in Complex with Fkbp12 and The Inhibitor E6201
  391. 3ui6: 0.89 a Resolution Crystal Structure of Human Parvulin 14 in Complex with Oxidized Dtt
  392. 4fru: Crystal Structure of Horse Wild-type Cyclophilin B
  393. 4frv: Crystal Structure of Mutated Cyclophilin B That Causes Hyperelastosis Cutis in The American Quarter Horse
  394. 4drh: Co-crystal Structure of The Ppiase Domain of Fkbp51, Rapamycin and The Frb Fragment of Mtor at Low Ph
  395. 4dri: Co-crystal Structure of The Ppiase Domain of Fkbp51, Rapamycin and The Frb Fragment of Mtor
  396. 4drj: O-crystal Structure of The Ppiase Domain of Fkbp52, Rapamycin and The Frb Fragment of Mtor
  397. 6hmz: Crystal Structure of a Single-domain Cyclophilin from Brassica Napus Phloem Sap
  398. 6h3j: Structural Snapshots of The Type 9 Protein Translocon Plug-complex
  399. 6h3i: Structural Snapshots of The Type 9 Protein Translocon
  400. 4e1q: Crystal Structure of Wheat Cyclophilin a at 1.25 a Resolution
  401. 4hy7: Structural and Biochemical Characterization of a Cytosolic Wheat Cyclophilin Tacypa-1
  402. 6gs6: Cyclophilin a Single Mutant D66A in Complex with an Inhibitor.
  403. 4itz: Crystal Structure of The Fk506 Binding Domain of Plasmodium Vivax Fkbp35 in Complex with a Tetrapeptide Substrate
  404. 4jcp: Structure of Cyclophilin B from Brugia Malayi
  405. 6gjy: Cyclophilin a Complexed with Tri-vector Ligand 5.
  406. 6gjr: Cyclophilin a Complexed with Tri-vector Ligand 9.
  407. 6gjp: Cyclophilin a Complexed with Tri-vector Ligand 7.
  408. 6gjn: Cyclophilin a Complexed with Tri-vector Ligand 15.
  409. 6gjm: Cyclophilin a Complexed with Tri-vector Ligand 4.
  410. 6gjl: Cyclophilin a Complexed with Tri-vector Ligand 10.
  411. 6gjj: Cyclophilin a Complexed with Tri-vector Ligand 2.
  412. 6gji: Cyclophilin a Complexed with The Tri-vector Ligand 8.
  413. 4eyv: Crystal Structure of Cyclophilin a like Protein from Piriformospora Indica
  414. 6vj2: 3.10 Angstrom Resolution Crystal Structure of Foldase Protein (prsa) from Lactococcus Lactis
  415. 4ipx: Analyzing The Visible Conformational Substates of The Fk506 Binding Protein Fkbp12
  416. 4jjm: Structure of a Cyclophilin from Citrus Sinensis (cscyp) in Complex with Cycloporin a
  417. 6fk1: Cyclophilin a
  418. 6ff7: Human Bact Spliceosome Core Structure
  419. 6ff4: Human Bact Spliceosome Core Structure
  420. 4l6e: Crystal Structure of The Ranbd1 Fourth Domain of E3 Sumo-protein Ligase Ranbp2. Northeast Structural Genomics Consortium (nesg) Target HR9193B
  421. 4bf8: Fpr4 Ppi Domain
  422. 4c02: Crystal Structure of Human Acvr1 (alk2) in Complex with Fkbp12.6 and Dorsomorphin
  423. 2m1i: High Resolution Structure and Dynamics of Cspina Parvulin at Physiological Temperature
  424. 2m2a: Nmr Solution Structure of The Two Domain Ppiase Slpa from Escherichia Coli
  425. 6dun: Crystal Structure Analysis of Pin1
  426. 2m8i: Structure of Pin1 Ww Domain
  427. 2m8j: Structure of Pin1 Ww Domain Phospho-mimic S16E
  428. 2mc9: Cat R 1
  429. 2mf9: Solution Structure of The N-terminal Domain of Human Fkbp38 (FKBP38NTD)
  430. 2mlx: Nmr Structure of E. Coli Trigger Factor in Complex with Unfolded Phoa220-310
  431. 2mly: Nmr Structure of E. Coli Trigger Factor in Complex with Unfolded Phoa1-150
  432. 2mlz: Nmr Structure of E. Coli Trigger Factor in Complex with Unfolded Phoa365-471
  433. 6d6s: Solution Structure of Trigger Factor Dimer
  434. 3wh0: Structure of Pin1 Complex with 18-crown-6
  435. 4ca9: Structure of The Nucleoplasmin-like N-terminal Domain of Drosophila Fkbp39
  436. 6vj4: 1.70 Angstrom Resolution Crystal Structure of Peptidylprolyl Isomerase (prsa) from Bacillus Anthracis
  437. 6vj6: 2.55 Angstrom Resolution Crystal Structure of Peptidylprolyl Isomerase (prsa) from Bacillus Cereus
  438. 4gwt: Structure of Racemic Pin1 Ww Domain Cocrystallized with Dl-malic Acid
  439. 4gwv: Structure of Racemic Pin1 Ww Domain Cocrystallized with Tri-ammonium Citrate
  440. 4ipz: Smbz Bound to Cyclophilin a
  441. 4iq2: P21 Crystal Form of Fkbp12.6
  442. 4iqc: P3121 Crystal Form of Fkbp12.6
  443. 4j4n: Crystal Structure of Fk506 Binding Domain of Plasmodium Falciparum Fkbp35 in Complex with D44
  444. 4j4o: Crystal Structure of Fk506 Binding Domain of Plasmodium Vivax Fkbp35 in Complex with D44
  445. 4j58: Human Cyclophilin D Complexed with an Inhibitor
  446. 4j59: Human Cyclophilin D Complexed with an Inhibitor
  447. 4j5a: Human Cyclophilin D Complexed with an Inhibitor
  448. 4j5b: Human Cyclophilin D Complexed with an Inhibitor
  449. 4j5c: Human Cyclophilin D Complexed with an Inhibitor
  450. 4j5d: Human Cyclophilin D Complexed with an Inhibitor
  451. 4j5e: Human Cyclophilin D Complexed with an Inhibitor
  452. 4jfi: Increasing The Efficiency Efficiency of Ligands for The Fk506-binding Protein 51 by Conformational Control: Complex of Fkbp51 with Compound 1-[(9s,13r,13ar)-1,3-dimethoxy-8-oxo-5,8,9,10,11,12,13,13a-octahydro- 6h-9,13-epiminoazocino[2,1-a]isoquinolin-14-yl]-2-(3,4,5- Trimethoxyphenyl)ethane-1,2-dione
  453. 4jfj: Increasing The Efficiency Efficiency of Ligands for The Fk506-binding Protein 51 by Conformational Control: Complex of Fkbp51 with Compound (1s,6r)-10-(1,3-benzothiazol-6-ylsulfonyl)-3-[2-(3,4- Dimethoxyphenoxy)ethyl]-3,10-diazabicyclo[4.3.1]decan-2-one
  454. 4jfk: Increasing The Efficiency Efficiency of Ligands for The Fk506-binding Protein 51 by Conformational Control: Complex of Fkbp51 with (1s,6r)- 3-[2-(3,4-dimethoxyphenoxy)ethyl]-10-[(2-oxo-2,3-dihydro-1,3- Benzothiazol-6-yl)sulfonyl]-3,10-diazabicyclo[4.3.1]decan-2-one
  455. 4jfl: Increasing The Efficiency Efficiency of Ligands for The Fk506-binding Protein 51 by Conformational Control: Complex of Fkbp51 with 6-({(1s, 5r)-3-[2-(3,4-dimethoxyphenoxy)ethyl]-2-oxo-3,9- Diazabicyclo[3.3.1]non-9-yl}sulfonyl)-1,3-benzothiazol-2(3h)-one
  456. 4jfm: Increasing The Efficiency Efficiency of Ligands for The Fk506-binding Protein 51 by Conformational Control: Complex of Fkbp51 with 2-(3,4- Dimethoxyphenoxy)ethyl (2s)-1-[(2-oxo-2,3-dihydro-1,3-benzothiazol-6- Yl)sulfonyl]piperidine-2-carboxylate
  457. 4lac: Crystal Structure of Protein Phosphatase 2a (PP2A) and PP2A Phosphatase Activator (ptpa) Complex with Atpgammas
  458. 4lav: Crystal Structure Analysis of Fkbp52, Crystal Form II
  459. 4law: Crystal Structure Analysis of Fkbp52, Crystal Form III
  460. 4lax: Crystal Structure Analysis of Fkbp52, Complex with Fk506
  461. 4lay: Crystal Structure Analysis of Fkbp52, Complex with I63
  462. 4lqw: Crystal Structure of Hiv-1 Capsid N-terminal Domain in Complex with Nup358 Cyclophilin
  463. 4mgv: Crystal Structure of Fk506 Binding Domain of Plasmodium Vivax Fkbp35 in Complex with Inhibitor D5
  464. 4msp: Crystal Structure of Human Peptidyl-prolyl Cis-trans Isomerase Fkbp22 (aka Fkbp14) Containing Two Ef-hand Motifs
  465. 4n19: Structural Basis of Conformational Transitions in The Active Site and 80 S Loop in The Fk506 Binding Protein Fkbp12
  466. 4nnr: Fkbp13-fk506 Complex
  467. 4ny3: Human Ptpa in Complex with Peptide
  468. 4o8h: 0.85a Resolution Structure of Peg 400 Bound Cyclophilin D
  469. 4o8i: 1.45a Resolution Structure of Peg 400 Bound Cyclophilin D
  470. 5yba: Dimeric Cyclophilin from T.vaginalis in Complex with Myb1 Peptide
  471. 5yb9: Crystal Structure of a Dimeric Cyclophilin a from T.vaginalis
  472. 5xb0: 1.6 a Crystal Structure of Peptidyl-prolyl Cis-trans Isomerase Ppiase from Pseudomonas Syringae Pv. Tomato Str. Dc3000 (pspto Dc3000)
  473. 5wc7: Cypa Mutant - I97V S99T C115S
  474. 4r3e: Structure of a Spliceosomal Protein from Homo Sapiens
  475. 4r3f: Structure of a Spliceosomal Protein from Chaetomium Thermophilum
  476. 4tot: Crystal Structure of Rat Cyclophilin D in Complex with a Potent Nonimmunosuppressive Inhibitor
  477. 4tx0: The Fk1 Domain of Fkbp51 in Complex with (1s,5s,6r)-10-[(3,5- Dichlorophenyl)sulfonyl]-5-(2-methoxyethoxy)-3-(2-methoxyethyl)-3,10- Diazabicyclo[4.3.1]decan-2-one
  478. 4tyo: Ppiase in Complex with a Non-phosphate Small Molecule Inhibitor.
  479. 5v8t: Crystal Structure of Smt Fusion Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with Sf354
  480. 5uy9: Prolyl Isomerase Pin1 R14A Mutant Bound with Brd4 Peptide
  481. 4tw6: The Fk1 Domain of Fkbp51 in Complex with Ifit1
  482. 4tw7: The Fk1 Domain of Fkbp51 in Complex with Ifit4
  483. 4tw8: The Fk1-fk2 Domains of Fkbp52 in Complex with Ifit-fl
  484. 4w9o: The Fk1 Domain of Fkbp51 in Complex with (1s,5s,6r)-10-[(3,5- Dichlorophenyl)sulfonyl]-5-[(1r)-1,2-dihydroxyethyl]-3-[2-(3,4- Dimethoxyphenoxy)ethyl]-3,10-diazabicyclo[4.3.1]decan-2-one
  485. 4w9p: The Fk1 Domain of Fkbp51 in Complex with (1s,5s,6r)-10-[(3,5- Dichlorophenyl)sulfonyl]-5-[(1s)-1,2-dihydroxyethyl]-3-[2-(3,4- Dimethoxyphenoxy)ethyl]-3,10-diazabicyclo[4.3.1]decan-2-one
  486. 4w9q: The Fk1 Domain of Fkbp51 in Complex with (1s,5s,6r)-10-[(3,5- Dichlorophenyl)sulfonyl]-3-[2-(3,4-dimethoxyphenoxy)ethyl]-5-ethyl-3, 10-diazabicyclo[4.3.1]decan-2-one
  487. 2ruc: Solution Structure of The Peptidyl Prolyl Cis-trans Isomerase Domain of Human Pin1 with Sulfate Ion
  488. 2rud: Solution Structure of The Peptidyl Prolyl Cis-trans Isomerase Domain of C113D Mutant Human Pin1 with Sulfate Ion
  489. 5tvl: Crystal Structure of Foldase Protein Prsa from Streptococcus Pneumoniae Str. Canada Mdr_19a
  490. 5ta4: Discovery of a Potent Cyclophilin Inhibitor (compound 8) Based on Structural Simplification of Sanglifehrin a
  491. 5ta2: Discovery of a Potent Cyclophilin Inhibitor (compound 7) Based on Structural Simplification of Sanglifehrin a
  492. 5t9z: Discovery of a Potent Cyclophilin Inhibitor (compound 6) Based on Structural Simplification of Sanglifehrin a
  493. 5t9w: Discovery of a Potent Cyclophilin Inhibitor (compound 5) Based on Structural Simplification of Sanglifehrin a
  494. 5t9u: Discovery of a Potent Cyclophilin Inhibitor (compound 3) Based on Structural Simplification of Sanglifehrin a
  495. 5owj: The Dynamic Dimer Structure of The Chaperone Trigger Factor (conformer 2)
  496. 5owi: The Dynamic Dimer Structure of The Chaperone Trigger Factor (conformer 1)
  497. 5omp: Human Fkbp5 Protein
  498. 5obk: The Fk1 Domain of Fkbp51 in Complex with (1s,5s,6r)-10-((3,5- Dichlorophenyl)sulfonyl)-5-(hydroxymethyl)-3-(pyridin-2-ylmethyl)-3, 10-diazabicyclo[4.3.1]decan-2-one
  499. 5o9z: Cryo-em Structure of a Pre-catalytic Human Spliceosome Primed for Activation (b Complex)
  500. 5noz: Structure of Cyclophilin a in Complex with 3,4-diaminobenzohydrazide
  501. 5noy: Structure of Cyclophilin a in Complex with 3,4-diaminobenzamide
  502. 5nox: Structure of Cyclophilin a in Complex with 2-chloropyridin-3-amine
  503. 5now: Structure of Cyclophilin a in Complex with Pyridine-3,4-diamine
  504. 5nov: Structure of Cyclophilin a in Complex with Hexahydropyrimidine-2- Thione
  505. 5nou: Structure of Cyclophilin a in Complex with Hexahydropyrimidin-2-one
  506. 5not: Structure of Cyclophilin a in Complex with 4-chloropyrimidin-5-amine
  507. 5nos: Structure of Cyclophilin a in Complex with 3-amino-1h-pyridin-2-one
  508. 5nor: Structure of Cyclophilin a in Complex with 3-methylpyridin-2-amine
  509. 5noq: Structure of Cyclophilin a in Complex with 3-chloropyridin-2-amine
  510. 5njx: Human Fkbp51 Protein in Complex with C-terminal Peptide of Human Hsp 90-alpha
  511. 5mqf: Cryo-em Structure of a Human Spliceosome Activated for Step 2 of Splicing (c* Complex)
  512. 5mgx: The Structure of Fkbp38 in Complex with The Meevd Tetratricopeptide Binding-motif of Hsp90
  513. 5lud: Structure of Cyclophilin a in Complex with 2,3-diaminopyridine
  514. 5kv7: Human Cyclophilin a at 278k, Data Set 9
  515. 5kv6: Human Cyclophilin a at 278k, Data Set 8
  516. 5kv5: Human Cyclophilin a at 278k, Data Set 7
  517. 5kv4: Human Cyclophilin a at 278k, Data Set 6
  518. 5kv3: Human Cyclophilin a at 278k, Data Set 5
  519. 5kv2: Human Cyclophilin a at 278k, Data Set 4
  520. 5kv1: Human Cyclophilin a at 278k, Data Set 3
  521. 5kv0: Human Cyclophilin a at 278k, Data Set 2
  522. 5kuz: Human Cyclophilin a at 278k, Data Set 1
  523. 5kuw: Human Cyclophilin a at 100k, Data Set 9
  524. 5kuv: Human Cyclophilin a at 100k, Data Set 8
  525. 5kuu: Human Cyclophilin a at 100k, Data Set 7
  526. 5kus: Human Cyclophilin a at 100k, Data Set 6
  527. 5kur: Human Cyclophilin a at 100k, Data Set 5
  528. 5kuq: Human Cyclophilin a at 100k, Data Set 4
  529. 5kuo: Human Cyclophilin a at 100k, Data Set 3
  530. 5kun: Human Cyclophilin a at 100k, Data Set 2
  531. 5kul: Human Cyclophilin a at 100k, Data Set 1
  532. 5klx: Crystal Structure of Smt Fusion Peptidyl-prolyl Cis-trans Isomerase from Burkholderia Pseudomallei Complexed with Sf110
  533. 5jhe: The Crystal Structure of The Saccharomyces Cerevisiae Co-chaperone Cpr7
  534. 5j6e: Structure of Disulfide Crosslinked A. Fumigatus FKBP12(V91C)
  535. 5i98: Structure of Apo FKBP12(P104G) from C. Albicans
  536. 5i7q: Crystal Structure of Fkbp12-if(slpa), a Chimeric Protein of Human Fkbp12 and The Insert in Flap Domain of Ecoli Slpa
  537. 5i7p: Crystal Structure of Fkbp12-if(slyd), a Chimeric Protein of Human Fkbp12 and The Insert in Flap Domain of Ecoli Slyd
  538. 5hwc: Aspergillus Fumigatus Fkbp12 P90G Protein Bound with Fk506 in P212121 Space Group
  539. 5hwb: Aspergillus Fumigatus Fkbp12 Apo Protein in P212121 Space Group
  540. 5hw8: Candida Albicans Fkbp12 P104G Protein Bound with Fk506 in C2 Space Group
  541. 5hw7: Candida Albicans Fkbp12 Apo Protein in P21212 Space Group
  542. 5hw6: Candida Albicans Fkbp12 Apo Protein in C2 Space Group
  543. 5hua: Structure of C. Glabrata Fkbp12-fk506 Complex
  544. 5htg: Structure of Apo P1 Form of Candida Albicans Fkbp12
  545. 5htf: Crystal Structure of Prsa1 from Listeria Monocytogenes
  546. 5ht1: Structure of Apo C. Glabrata Fkbp12
  547. 5hsv: X-ray Structure of a Cypa-alisporivir Complex at 1.5 Angstrom Resolution
  548. 5hkg: Total Chemical Synthesis, Refolding and Crystallographic Structure of a Fully Active Immunophilin: Calstabin 2 (fkbp12.6).
  549. 5gph: Solution Structure of The Pin1-ppiase (S138A) Mutant
  550. 5gpg: Co-crystal Structure of The Fk506 Binding Domain of Human Fkbp25, Rapamycin and The Frb Domain of Human Mtor
  551. 5fjb: Cyclophilin a Stabilize Hiv-1 Capsid through a Novel Non- Canonical Binding Site
  552. 5f66: High-resolution Isotropic Multiconformer Synchrotron Model of Cypa at 273 K
  553. 5ez1: Crystal Structure of Cell Binding Factor 2 from Helicobacter Pylori in Complex with I2CA
  554. 5ex2: Crystal Structure of Cyclophilin Aquacyp293 from Hirschia Baltica
  555. 5div: The Fk1 Domain of Fkbp51 in Complex with The New Synthetic Ligand (s)- N-(1-carbamoylcyclopentyl)-1-((s)-2-cyclohexyl-2-(3,4,5- Trimethoxyphenyl)acetyl)piperidine-2-carboxamide
  556. 5diu: The Fk1 Domain of Fkbp51 in Complex with The New Synthetic Ligand 2- (3-((r)-1-((s)-1-((s)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl) Piperidine-2-carboxamido)-3-(3,4-dimethoxyphenyl)propyl)phenoxy) Acetic Acid
  557. 5dit: The Fk1 Domain of Fkbp51 in Complex with The New Synthetic Ligand (1r)-3-(3,4-dimethoxyphenyl)-1-f3-[2-(morpholin-4-yl) Ethoxy]phenylgpropyl(2s)-1-[(2s,3r)-2-cyclohexyl-3- Hydroxybutanoyl]piperidine-2-carboxylate
  558. 5d75: Crystal Structure of Human Fkbd25 in Complex with Fk506
  559. 5ccs: Human Cyclophilin D Complexed with Inhibitor
  560. 5ccr: Human Cyclophilin D Complexed with Inhibitor
  561. 5ccq: Human Cyclophilin D Complexed with Inhibitor
  562. 5ccn: Human Cyclophilin D Complexed with Inhibitor
  563. 5cbw: Human Cyclophilin D Complexed with Inhibitor.
  564. 5cbu: Human Cyclophilin D Complexed with Inhibitor.
  565. 5cbt: Human Cyclophilin D Complexed with Inhibitor
  566. 5bxj: Complex of The Fk1 Domain Mutant A19T of Fkbp51 with 4-nitrophenol
  567. 4wo7: Crystal Structure of Prsa from Bacillus Subtilis
  568. 4odk: Structure of Slyd from Thermus Thermophilus in Complex with T1 Peptide
  569. 4odl: Structure of Slyd from Thermus Thermophilus in Complex with S2 Peptide
  570. 4odm: Structure of Slyd from Thermus Thermophilus in Complex with S2-W23A Peptide
  571. 4odn: Structure of Slyd from Thermus Thermophilus in Complex with S2-plus Peptide
  572. 4odo: Structure of Slyd from Thermus Thermophilus in Complex with Fk506
  573. 4odp: Structure of Slyd Delta-if from Thermus Thermophilus in Complex with S2-W23A Peptide
  574. 4odq: Structure of Slyd Delta-if from Thermus Thermophilus in Complex with S3 Peptide
  575. 4odr: Structure of Slyd Delta-if from Thermus Thermophilus in Complex with Fk506
  576. 4qib: Oxidation-mediated Inhibition of The Peptidyl-prolyl Isomerase Pin1
  577. 5bmy: Crystal Structure of Hpin1 Ww Domain (5-21) Fused with Maltose-binding Protein
  578. 5a0e: Crystal Structure of Cyclophilin D in Complex with Csa Analogue, Jw47.
  579. 4zsd: Human Cyclophilin D Complexed with an Inhibitor at Room Temperature
  580. 4zsc: Human Cyclophilin D Complexed with an Inhibitor at Room Temperature
  581. 4s1j: Crystal Structure of Cyclophilin Mutant V33A from Leishmania Donovani at 2.3 Angstrom.
  582. 4s1e: Crystal Structure of Cyclophilin Mutant L120A from Leishmania Donovani at 2.22 Angstrom.
  583. 4tns: Structure of Pin1 Ppiase Domain Bound with All-trans Retinoic Acid
  584. 4u84: Human Pin1 with S-hydroxyl-cysteine 113
  585. 4u85: Human Pin1 with Cysteine Sulfinic Acid 113
  586. 4u86: Human Pin1 with Cysteine Sulfonic Acid 113
  587. 4yup: Multiconformer Fixed-target X-ray Free Electron (xfel) Model of Cypa at 273 K
  588. 4yun: Multiconformer Synchrotron Model of Cypa at 310 K
  589. 4yum: Multiconformer Synchrotron Model of Cypa at 300 K
  590. 4yul: Multiconformer Synchrotron Model of Cypa at 280 K
  591. 4yuk: Multiconformer Synchrotron Model of Cypa at 260 K
  592. 4yuj: Multiconformer Synchrotron Model of Cypa at 240 K
  593. 4yui: Multiconformer Synchrotron Model of Cypa at 180 K
  594. 4yuh: Multiconformer Synchrotron Model of Cypa at 150 K
  595. 4yug: Multiconformer Synchrotron Model of Cypa at 100 K
  596. 2mph: Solution Structure of Human Fk506 Binding Protein 25
  597. 2mzu: Extending The Enoe Data Set of Large Proteins by Evaluation of Noes with Unresolved Diagonals
  598. 4r0x: Allosteric Coupling of Conformational Transitions in The Fk1 Domain of Fkbp51 near The Site of Steroid Receptor Interaction
  599. 4yuo: High-resolution Multiconformer Synchrotron Model of Cypa at 273 K
  600. 2ms4: Cyclophilin a Complexed with a Fragment of Crk-ii
  601. 2mvz: Solution Structure for Cyclophilin a from Geobacillus Kaustophilus
  602. 2n0t: Structural Ensemble of The Enzyme Cyclophilin Reveals an Orchestrated Mode of Action at Atomic Resolution
  603. 2n1o: Pin1 Ww Domain in Complex with a Phosphorylated Cpeb1 Derived Peptide
  604. 2nd5: Lysine Dimethylated Fkbp12
  605. 2ruq: Solution Structure of Human Pin1 Ppiase Mutant C113A
  606. 2rur: Solution Structure of Human Pin1 Ppiase C113S Mutant
  607. 3jb9: Cryo-em Structure of The Yeast Spliceosome at 3.6 Angstrom Resolution
  608. 4n1m: Structure of Cyclophilin a in Complex with Glypro.
  609. 4n1n: Structure of Cyclophilin a in Complex with Benzamide.
  610. 4n1o: Structure of Cyclophilin a in Complex with Saccharin.
  611. 4n1p: Structure of Cyclophilin a in Complex with Picolinamide.
  612. 4n1q: Structure of Cyclophilin a in Complex with Cyclohexanecarboxamide.
  613. 4n1r: Structure of Cyclophilin a in Complex with Benzenesulfonohydrazide.
  614. 4n1s: Structure of Cyclophilin a in Complex with Benzohydrazide.
  615. 4qt2: Crystal Structure of The Fk506-binding Domain of Plasmodium Falciparum Fkbp35 in Complex with Rapamycin
  616. 4qt3: Crystal Structure Resolution of Plasmodium Falciparum Fk506 Binding Domain (fkbp35) in Complex with Rapamycin at 1.4a Resolution
  617. 4xnc: Crystal Structure at Room Temperature of Cyclophilin D in Complex with an Inhibitor
  618. 6vaj: Crystal Structure Analysis of Human Pin1
  619. 6x34: Pig R615C Ryr1 Egta (all Classes, Open)
  620. 7abi: Human Pre-bact-2 Spliceosome
  621. 6yf0: Fkbp12 in Complex with The Bmp Potentiator Compound 9 at 1.55 a Resolution
  622. 6yf1: Fkbp12 in Complex with The Bmp Potentiator Compound 8 at 1.12a Resolution
  623. 6yf2: Fkbp12 in Complex with The Bmp Potentiator Compound 6 at 1.03a Resolution
  624. 6yf3: Fkbp12 in Complex with The Bmp Potentiator Compound 10 at 1.00a Resolution
  625. 7awx: Structure of The FKBP51FK1 Domain in Complex with The Macrocyclic Safit Analogue 55
  626. 7b9y: Structure of The FKBP51FK1 Domain in Complex with The Macrocyclic Safit Analogue 64a
  627. 7b9z: Structure of The FKBP51FK1 Domain in Complex with The Macrocyclic Safit Analogue 35-(e)
  628. 7ba0: Structure of The FKBP51FK1 Domain in Complex with The Macrocyclic Safit Analogue 63
  629. 6wbu: Putative Peptidyl Prolyl Cis-trans Isomerase Fkbp12 from Mycobacterium Tuberculosis
  630. 7dvq: Cryo-em Structure of The Activated Human Minor Spliceosome (minor Bact Complex)
  631. 7kkf: Crystal Structure of S. Cerevisiae Ess1
  632. 7aot: The Fk1 Domain of Fkbp51 in Complex with (2r,5s,12r)-12-cyclohexyl-2- [2-(3,4-dimethoxyphenyl)ethyl]-3,19-dioxa-10,13,16- Triazatricyclo[18.3.1.0-5,10]tetracosa- 1(24),20,22-triene-4,11,14, 17-tetrone
  633. 7aou: The Fk1 Domain of Fkbp51 in Complex with (2'r,5's,12'r)-12'- Cyclohexyl-2'-[2-(3,4-dimethoxyphenyl)ethyl]-3',19'-dioxa-10',13', 16'-triazaspiro[cyclopropane-1,15'- Tricyclo[18.3.1.0-5, 10]tetracosane]-1'(24'),20',22'-triene-4',11',14',17'-tetrone
  634. 7awf: The Fk1 Domain of Fkbp51 in Complex with (2r,5s,12r)-12-cyclohexyl-2- [2-(3,4-dimethoxyphenyl)ethyl]-15,15,16-trimethyl-3,19-dioxa-10,13, 16-triazatricyclo[18.3.1.0^5,^10]tetracosa-1(24),20,22-triene-4,11, 14,17-tetrone
  635. 7aog: 14-3-3 Sigma in Complex with Pin1 Binding Site Ps72
  636. 7axn: 14-3-3 Sigma in Complex with Pin1 Binding Site Ps72 and Covalently Bound Tcf521-026
  637. 7ayf: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Tcf521- 110
  638. 7az1: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1013
  639. 7az2: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1014
  640. 7bdp: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1017
  641. 7bdt: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1009
  642. 7bdy: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound PC2068B
  643. 7bfw: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound PC2068A
  644. 7bg3: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Pc2046
  645. 7bgq: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1019
  646. 7bgr: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1016
  647. 7bgv: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1012
  648. 7bgw: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1011
  649. 7nif: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Tcf521- 011
  650. 7nig: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1008
  651. 7nj6: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1005
  652. 7nj8: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1007
  653. 7nja: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1006
  654. 7nrk: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound LVD1002F1
  655. 7nrl: 14-3-3 Sigma with Pin1 Binding Site Ps72 and Covalently Bound Lvd1032
  656. 7abt: Structure of Ppia in Complex with Pr Dipeptide Repeat
  657. 7epd: Cryo-em Structure of Inactive Mglu2-7 Heterodimer
  658. 7l7i: Cryo-em Structure of Hsp90:fkbp51:p23 Closed-state Complex
  659. 7dek: Pseudomonas Aeruginosa Fk506-binding Protein Pafkba
  660. 7n3j: E. Coli Peptidyl-prolyl Cis-trans Isomerase, Mutant PHE27CF3- TYR/PHE98CF3-TYR
  661. 7rfd: E. Coli Peptidyl-prolyl Cis-trans Isomerase, Mutant PHE4ALA PHE27CF3- PHE/PHE98CF3-PHE
  662. 7sa5: Two-state Solution Nmr Structure of Apo Pin1
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