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: 6 January 2022, 2:15

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
663. 7aps: The Fk1 Domain of Fkbp51 in Complex with (2s)-2-((1s,5r,6r)-10-((3,5- Dichlorophenyl)sulfonyl)-2-oxo-5-vinyl-3,10-diazabicyclo[4.3.1]decan- 3-yl)propanoic Acid
664. 7apq: The Fk1 Domain of Fkbp51 in Complex with (1s,5s,6r)-10- (benzo[d]thiazol-6-ylsulfonyl)-5-(methoxymethyl)-3-(pyridin-2- Ylmethyl)-3,10-diazabicyclo[4.3.1]decan-2-one
665. 7apt: The Fk1 Domain of Fkbp51 in Complex with ((1s,5s,6r)-10-((3,5- Dichlorophenyl)sulfonyl)-2-oxo-5-vinyl-3,10-diazabicyclo[4.3.1]decan- 3-yl)acetic Acid
666. 7apw: The Fk1 Domain of Fkbp51 in Complex with (1s,5s,6r)-10- (benzo[d]thiazol-6-ylsulfonyl)-5-(methoxymethyl)-3-(pyridin-2- Ylethyl)-3,10-diazabicyclo[4.3.1]decan-2-one
667. 7l6y: Crystal Structure of The Peptidyl-prolyl Cis-trans Isomerase (ppib) from Streptococcus Pyogenes.
668. 7l6z: Crystal Structure of Peptidyl-prolyl Cis-trans Isomerasefrom (ppib) Streptococcus Pneumoniae R6
669. 7l75: Crystal Structure of Peptidylprolyl Isomerase Prsa from Streptococcus Mutans.