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enzyme (lysozyme)

 
Enzymes
  Enzyme classes:
  EC 1: Oxidoreductases
  EC 2: Transferases
  EC 3: Hydrolases
    EC 3.1
    EC 3.2
    EC 3.3
    EC 3.4
      EC 3.4.1
      EC 3.4.2
      EC 3.4.3
      EC 3.4.4
      EC 3.4.11
      EC 3.4.12
      EC 3.4.13
      EC 3.4.14
      EC 3.4.15
      EC 3.4.16
      EC 3.4.17
      EC 3.4.18
      EC 3.4.19
      EC 3.4.21
      EC 3.4.22
      EC 3.4.23
        EC 3.4.23.1
        EC 3.4.23.2
        EC 3.4.23.3
        EC 3.4.23.4
        EC 3.4.23.5
        EC 3.4.23.6
        EC 3.4.23.7
        EC 3.4.23.8
        EC 3.4.23.9
        EC 3.4.23.10
        EC 3.4.23.11
        EC 3.4.23.12
        EC 3.4.23.13
        EC 3.4.23.14
        EC 3.4.23.15
        EC 3.4.23.16
        EC 3.4.23.17
        EC 3.4.23.18
        EC 3.4.23.19
        EC 3.4.23.20
        EC 3.4.23.21
        EC 3.4.23.22
        EC 3.4.23.23
        EC 3.4.23.24
        EC 3.4.23.25
        EC 3.4.23.26
        EC 3.4.23.27
        EC 3.4.23.28
        EC 3.4.23.29
        EC 3.4.23.30
        EC 3.4.23.31
        EC 3.4.23.32
        EC 3.4.23.33
        EC 3.4.23.34
        EC 3.4.23.35
        EC 3.4.23.36
        EC 3.4.23.37
        EC 3.4.23.38
        EC 3.4.23.39
        EC 3.4.23.40
        EC 3.4.23.41
        EC 3.4.23.42
        EC 3.4.23.43
        EC 3.4.23.44
        EC 3.4.23.45
        EC 3.4.23.46
        EC 3.4.23.47
        EC 3.4.23.48
        EC 3.4.23.49
      EC 3.4.24
      EC 3.4.25
      EC 3.4.99
    EC 3.5
    EC 3.6
    EC 3.7
    EC 3.8
    EC 3.9
    EC 3.10
    EC 3.11
    EC 3.12
    EC 3.13
  EC 4: Lyases
  EC 5: Isomerases
  EC 6: Ligases
  General information:
  Catalytic mechanism
  Enzyme kinetics
  Inhibitors
  Enzymes in industry

EC 3.4.23.16 - HIV- 1 retropepsin



3D structures of EC 3.4.23.16 - HIV-1 retropepsin in Protein Data Bank

updated: 6 January 2022, 2:15

In total: 561 PDB structures of EC 3.4.23.16 - HIV-1 retropepsin:
  1. 1a30: Hiv-1 Protease Complexed with a Tripeptide Inhibitor
  2. 1a8g: Hiv-1 Protease in Complex with Sdz283-910
  3. 1a8k: Crystallographic Analysis of Human Immunodeficiency Virus 1 Protease with an Analog of The Conserved Ca-p2 Substrate: Interactions with Frequently Occurring Glutamic Acid Residue at P2' Position of Substrates
  4. 1a94: Structural Basis for Specificity of Retroviral Proteases
  5. 1aid: Structure of a Non-peptide Inhibitor Complexed with Hiv-1 Protease: Developing a Cycle of Structure-based Drug Design
  6. 1ajv: Hiv-1 Protease in Complex with The Cyclic Sulfamide Inhibitor Aha006
  7. 1ajx: Hiv-1 Protease in Complex with The Cyclic Urea Inhibitor Aha001
  8. 1axa: Active-site Mobility in Human Immunodeficiency Virus Type 1 Protease as Demonstrated by Crystal Structure of A28S Mutant
  9. 1az5: Unliganded Siv Protease Structure in an "open" Conformation
  10. 1b11: Structure of Feline Immunodeficiency Virus Protease Complexed with Tl-3-093
  11. 1b6j: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 1
  12. 1b6k: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 5
  13. 1b6l: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 4
  14. 1b6m: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 6
  15. 1b6p: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 7
  16. 1bdl: Hiv-1 (2:31-37) Protease Complexed with Inhibitor Sb203386
  17. 1bdq: Hiv-1 (2:31-37, 47, 82) Protease Complexed with Inhibitor Sb203386
  18. 1bdr: Hiv-1 (2: 31, 33-37) Protease Complexed with Inhibitor Sb203386
  19. 1bv7: Counteracting Hiv-1 Protease Drug Resistance: Structural Analysis of Mutant Proteases Complexed with Xv638 and Sd146, Cyclic Urea Amides with Broad Specificities
  20. 1bv9: Hiv-1 Protease (I84V) Complexed with Xv638 of Dupont Pharmaceuticals
  21. 1bve: Hiv-1 Protease-dmp323 Complex in Solution, Nmr, 28 Structures
  22. 1bvg: Hiv-1 Protease-dmp323 Complex in Solution, Nmr Minimized Average Structure
  23. 1bwa: Hiv-1 Protease (V82F/I84V) Double Mutant Complexed with Xv638 of Dupont Pharmaceuticals
  24. 1bwb: Hiv-1 Protease (V82F/I84V) Double Mutant Complexed with Sd146 of Dupont Pharmaceuticals
  25. 1d4h: Hiv-1 Protease in Complex with The Inhibitor Bea435
  26. 1d4i: Hiv-1 Protease in Complex with The Inhibitor Bea425
  27. 1d4j: Hiv-1 Protease in Complex with The Inhibitor Msl370
  28. 1d4k: Hiv-1 Protease Complexed with a Macrocyclic Peptidomimetic Inhibitor
  29. 1d4l: Hiv-1 Protease Complexed with a Macrocyclic Peptidomimetic Inhibitor
  30. 1d4s: Hiv-1 Protease V82F/I84V Double Mutant/tipranavir Complex
  31. 1d4y: Hiv-1 Protease Triple Mutant/tipranavir Complex
  32. 1daz: Structural and Kinetic Analysis of Drug Resistant Mutants of Hiv-1 Protease
  33. 1dmp: Structure of Hiv-1 Protease Complex
  34. 1dw6: Structural and Kinetic Analysis of Drug Resistant Mutants of Hiv-1 Protease
  35. 1ebk: Structural and Kinetic Analysis of Drug Resistant Mutants of Hiv-1 Protease
  36. 1ebw: Hiv-1 Protease in Complex with The Inhibitor Bea322
  37. 1eby: Hiv-1 Protease in Complex with The Inhibitor Bea369
  38. 1ebz: Hiv-1 Protease in Complex with The Inhibitor Bea388
  39. 1ec0: Hiv-1 Protease in Complex with The Inhibitor Bea403
  40. 1ec1: Hiv-1 Protease in Complex with The Inhibitor Bea409
  41. 1ec2: Hiv-1 Protease in Complex with The Inhibitor Bea428
  42. 1ec3: Hiv-1 Protease in Complex with The Inhibitor Msa367
  43. 1f7a: How Does a Symmetric Dimer Recognize an Asymmetric Substrate? a Substrate Complex of Hiv-1 Protease.
  44. 1fej: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
  45. 1ff0: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes.
  46. 1fff: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease : High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes.
  47. 1ffi: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
  48. 1fg6: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
  49. 1fg8: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
  50. 1fgc: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
  51. 1fiv: Structure of an Inhibitor Complex of Proteinase from Feline Immunodeficiency Virus
  52. 1fmb: Eiav Protease Complexed with The Inhibitor Hby-793
  53. 1fqx: Crystal Structure of The Complex of Hiv-1 Protease with a Peptidomimetic Inhibitor
  54. 1g2k: Hiv-1 Protease with Cyclic Sulfamide Inhibitor, Aha047
  55. 1g35: Crystal Structure of Hiv-1 Protease in Complex with Inhibitor, Aha024
  56. 1g6l: 1.9a Crystal Structure of Tethered Hiv-1 Protease
  57. 1hpo: Hiv-1 Protease Triple Mutant/u103265 Complex
  58. 1hvh: Nonpeptide Cyclic Cyanoguanidines as Hiv Protease Inhibitors
  59. 1hwr: Molecular Recognition of Cyclic Urea Hiv Protease Inhibitors
  60. 1hxb: Hiv-1 Proteinase Complexed with Ro 31-8959
  61. 1hxw: Hiv-1 Protease Dimer Complexed with A-84538
  62. 1iiq: Crystal Structure of Hiv-1 Protease Complexed with a Hydroxyethylamine Peptidomimetic Inhibitor
  63. 1izh: Inhibitor of Hiv Protease with Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants
  64. 1izi: Inhibitor of Hiv Protease with Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants
  65. 1jld: Potent Hiv Protease Inhibitors Containing a Novel (hydroxyethyl)amide Isostere
  66. 1k1t: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
  67. 1k1u: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
  68. 1k2b: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
  69. 1k2c: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
  70. 1k6c: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
  71. 1k6p: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
  72. 1k6t: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
  73. 1k6v: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
  74. 7upj: Hiv-1 Protease/u101935 Complex
  75. 6upj: Hiv-2 Protease/u99294 Complex
  76. 6fiv: Structural Studies of Hiv and Fiv Proteases Complexed with an Efficient Inhibitor of Fiv Pr
  77. 5upj: Hiv-2 Protease/u99283 Complex
  78. 5fiv: Structural Studies of Hiv and Fiv Proteases Complexed with an Efficient Inhibitor of Fiv Pr
  79. 4upj: Human Immunodeficiency Virus Type 2 Protease Mutant with Lys 57 Replaced by Leu (K57L) Complex with U097410 [4- Hydroxy-3-[1-[3-[[[[(tert-butyloxycarbonyl) Aminomethyl]carbonyl]amino]phenyl]propyl]coumarin
  80. 4fiv: Fiv Protease Complexed with an Inhibitor Lp-130
  81. 3upj: Human Immunodeficiency Virus Type 2 Protease Mutant with Lys 57 Replaced by Leu (K57L) Complex with U096333 [4- Hydroxy-3-[1-(phenyl)propyl]-7-methoxycoumarin]
  82. 3tlh: Structural Studies of Hiv and Fiv Proteases Complexed Withan Efficient Inhibitor of Fiv Pr
  83. 1kj4: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
  84. 1kj7: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
  85. 1kjf: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
  86. 1kjg: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
  87. 1kjh: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
  88. 3oxc: Wild Type Hiv-1 Protease with Antiviral Drug Saquinavir
  89. 1kzk: Je-2147-hiv Protease Complex
  90. 3ok9: Crystal Structure of Wild-type Hiv-1 Protease with New Oxatricyclic Designed Inhibitor Grl-0519a
  91. 3nuo: Crystal Structure of Hiv-1 Protease Mutant L90M with Antiviral Drug Amprenavir
  92. 3nuj: Crystal Structure of Hiv-1 Protease Mutant I54V with Antiviral Drug Amprenavir
  93. 3nu9: Crystal Structure of Hiv-1 Protease Mutant I84V with Antiviral Drug Amprenavir
  94. 3nu6: Crystal Structure of Hiv-1 Protease Mutant I54M with Antiviral Drug Amprenavir
  95. 3nu5: Crystal Structure of Hiv-1 Protease Mutant I50V with Antiviral Drug Amprenavir
  96. 3nu4: Crystal Structure of Hiv-1 Protease Mutant V32I with Antiviral Drug Amprenavir
  97. 3nu3: Wild Type Hiv-1 Protease with Antiviral Drug Amprenavir
  98. 1lv1: Crystal Structure Analysis of The Non-active Site Mutant of Tethered Hiv-1 Protease to 2.1a Resolution
  99. 1lzq: Crystal Structure of The Complex of Mutant Hiv-1 Protease (A71V, V82T, I84V) with an Ethylenamine Peptidomimetic Inhibitor BOC-PHE-PSI[CH2CH2NH]-PHE-GLU-PHE-NH2
  100. 1m0b: Hiv-1 Protease in Complex with an Ethyleneamine Inhibitor
  101. 3n3i: Crystal Structure of G48V/C95F Tethered Hiv-1 Protease/saquinavir Complex
  102. 1mer: Hiv-1 Mutant (I84V) Protease Complexed with Dmp450
  103. 1mes: Hiv-1 Mutant (I84V) Protease Complexed with Dmp323
  104. 1met: Hiv-1 Mutant (V82F) Protease Complexed with Dmp323
  105. 1meu: Hiv-1 Mutant (V82F, I84V) Protease Complexed with Dmp323
  106. 3mxe: Crystal Structure of Hiv-1 Protease Inhibitor, Kc32 Complexed with Wild-type Protease
  107. 3mxd: Crystal Structure of Hiv-1 Protease Inhibitor Kc53 in Complex with Wild-type Protease
  108. 1mrw: Structure of Hiv Protease (mutant Q7K L33I L63I) Complexed with Kni-577
  109. 1mrx: Structure of Hiv Protease (mutant Q7K L33I L63I V82F I84V ) Complexed with Kni-577
  110. 1msm: The Hiv Protease (mutant Q7K L33I L63I) Complexed with Kni- 764 (an Inhibitor)
  111. 1msn: The Hiv Protease (mutant Q7K L33I L63I V82F I84V) Complexed with Kni-764 (an Inhibitor)
  112. 1mt7: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
  113. 1mt8: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
  114. 1mt9: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
  115. 1mtb: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
  116. 1mtr: Hiv-1 Protease Complexed with a Cyclic Phe-ile-val Peptidomimetic Inhibitor
  117. 1mui: Crystal Structure of Hiv-1 Protease Complexed with Lopinavir.
  118. 1n49: Viability of a Drug-resistant Hiv-1 Protease Variant: Structural Insights for Better Anti-viral Therapy
  119. 3lzv: Structure of Nelfinavir-resistant Hiv-1 Protease (D30N/N88D) in Complex with Darunavir.
  120. 3lzu: Crystal Structure of a Nelfinavir Resistant Hiv-1 Crf01_ae Protease Variant (N88S) in Complex with The Protease Inhibitor Darunavir.
  121. 3lzs: Crystal Structure of Hiv-1 Crf01_ae Protease in Complex with Darunavir
  122. 1nh0: 1.03 a Structure of Hiv-1 Protease: Inhibitor Binding inside and outside The Active Site
  123. 1npa: Crystal Structure of Hiv-1 Protease-hup
  124. 1npv: Crystal Structure of Hiv-1 Protease Complexed with Ldc271
  125. 1npw: Crystal Structure of Hiv Protease Complexed with Lgz479
  126. 3kt2: Crystal Structure of N88D Mutant Hiv-1 Protease
  127. 1odw: Native Hiv-1 Proteinase
  128. 1odx: Hiv-1 Proteinase Mutant A71T, V82A
  129. 1ody: Hiv-1 Protease Complexed with an Inhibitor Lp-130
  130. 3kfs: Hiv Protease (pr) Dimer with Inhibitor Tl-3 Bound and Fragment 2f4 in The Outside/top of Flap
  131. 3kfr: Hiv Protease (pr) Dimer with Inhibitor Tl-3 Bound and Fragment 1f1 in The Outside/top of Flap
  132. 3kfp: Hiv Protease (pr) with Inhibitor Tl-3 Bound, and Dmsos in Exo Site
  133. 3kfn: Hiv Protease (pr) with Inhibitor Tl-3 and Fragment Hit 4d9 by Soaking
  134. 3kf0: Hiv Protease with Fragment 4d9 Bound
  135. 3kdd: Crystal Structure of Hiv-1 Protease (Q7K, L33I, L63I) in Complex with Kni-10265
  136. 3kdc: Crystal Structure of Hiv-1 Protease (Q7K, L33I, L63I) in Complex with Kni-10074
  137. 3kdb: Crystal Structure of Hiv-1 Protease (Q7K, L33I, L63I) in Complex with Kni-10006
  138. 3k4v: New Crystal Form of Hiv-1 Protease/saquinavir Structure Reveals Carbamylation of N-terminal Proline
  139. 3jw2: Hiv-1 Protease Mutant G86S with Darunavir
  140. 3jvy: Hiv-1 Protease Mutant G86A with Darunavir
  141. 3jvw: Hiv-1 Protease Mutant G86A with Symmetric Inhibitor Dmp323
  142. 1pro: Hiv-1 Protease Dimer Complexed with A-98881
  143. 3i8w: Crystal Structure of a Metallacarborane Inhibitor Bound to Hiv Protease
  144. 3i6o: Crystal Structure of Wild Type Hiv-1 Protease with Macrocyclic Inhibitor Grl-0216a
  145. 1q94: Structures of Hla-a*1101 in Complex with Immunodominant Nonamer and Decamer Hiv-1 Epitopes Clearly Reveal The Presence of a Middle Anchor Residue
  146. 1q9p: Solution Structure of The Mature Hiv-1 Protease Monomer
  147. 1qbr: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
  148. 1qbs: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
  149. 1qbt: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
  150. 1qbu: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
  151. 3hdk: Crystal Structure of Chemically Synthesized [aib51/51']hiv-1 Protease
  152. 3hbo: Crystal Structure of Chemically Synthesized [d-ala51/51']hiv-1 Protease
  153. 3h5b: Crystal Structure of Wild Type Hiv-1 Protease with Novel P1'-ligand Grl-02031
  154. 1rl8: Crystal Structure of The Complex of Resistant Strain of Hiv- 1 PROTEASE(V82A Mutant) with Ritonavir
  155. 1rpi: Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity
  156. 1rq9: Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity
  157. 3ggu: Hiv Pr Drug Resistant Patient's Variant in Complex with Darunavir
  158. 1rv7: Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity
  159. 3fx5: Structure of Hiv-1 Protease in Complex with Potent Inhibitor Kni-272 Determined by High Resolution X-ray Crystallography
  160. 3fsm: Crystal Structure of a Chemically Synthesized 203 Amino Acid 'covalent Dimer' [l-ala51,d-ala51'] Hiv-1 Protease Molecule
  161. 1sdt: Crystal Structures of Hiv Protease V82A and L90M Mutants Reveal Changes in Indinavir Binding Site.
  162. 1sdu: Crystal Structures of Hiv Protease V82A and L90M Mutants Reveal Changes in Indinavir Binding Site.
  163. 1sdv: Crystal Structures of Hiv Protease V82A and L90M Mutants Reveal Changes in Indinavir Binding Site.
  164. 1sgu: Comparing The Accumulation of Active Site and Non-active Site Mutations in The Hiv-1 Protease
  165. 1sh9: Comparing The Accumulation of Active Site and Non-active Site Mutations in The Hiv-1 Protease
  166. 3fiv: Crystal Structure of Feline Immunodeficiency Virus Protease Complexed with a Substrate
  167. 1sp5: Crystal Structure of Hiv-1 Protease Complexed with a Product of Autoproteolysis
  168. 1t3r: Hiv Protease Wild-type in Complex with Tmc114 Inhibitor
  169. 1t7i: The Structural and Thermodynamic Basis for The Binding of Tmc114, a Next-generation Hiv-1 Protease Inhibitor.
  170. 1t7j: Crystal Structure of Inhibitor Amprenavir in Complex with a Multi-drug Resistant Variant of Hiv-1 Protease (L63P/V82T/I84V)
  171. 1t7k: Crystal Structure of Hiv Protease Complexed with Arylsulfonamide Azacyclic Urea
  172. 3em6: Crystal Structure of I50L/A71V Mutant of Hiv-1 Protease in Complex with Inhibitor Darunavir
  173. 3em4: Crystal Structure of Atazanavir (atv) in Complex with I50L/A71V Drug-resistant Hiv-1 Protease
  174. 3em3: Crystal Structure of Amprenavir (apv) in Complex with a Drug Resistant Hiv-1 Protease Variant (I50L/A71V).
  175. 1tcw: Siv Protease Complexed with Inhibitor Sb203386
  176. 1tcx: Hiv Triple Mutant Protease Complexed with Inhibitor Sb203386
  177. 3el9: Crystal Structure of Atazanavir (atv) in Complex with a Multidrug Hiv-1 Protease (V82T/I84V)
  178. 3el4: Crystal Structure of Inhibitor Saquinavir (sqv) Complexed with The Multidrug Hiv-1 Protease Variant L63P/V82T/I84V
  179. 3el1: Crystal Structure of Wild-type Hiv Protease in Complex with The Inhibitor, Atazanavir
  180. 3el0: Crystal Structure of The Inhibitor Nelfinavir (nfv) in Complex with a Multi-drug Resistant Hiv-1 Protease Variant (L10I/G48V/I54V/V64I/V82A) (refer: Flap+ in Citation)
  181. 3eky: Crystal Structure of Wild-type Hiv Protease in Complex with The Inhibitor, Atazanavir
  182. 3ekx: Crystal Structure of The Wild-type Hiv-1 Protease with The Inhibitor, Nelfinavir
  183. 3ekw: Crystal Structure of The Inhibitor Atazanavir (atv) in Complex with a Multi-drug Resistance Hiv-1 Protease Variant (L10I/G48V/I54V/V64I/V82A) Refer: Flap+ in Citation.
  184. 3ekv: Crystal Structure of The Wild Type Hiv-1 Protease with The Inhibitor, Amprenavir
  185. 3ekt: Crystal Structure of The Inhibitor Darunavir (drv) in Complex with a Multi-drug Resistant Hiv-1 Protease Variant (L10F/G48V/I54V/V64I/V82A) (refer: Flap+ in Citation.)
  186. 3ekq: Crystal Structure of Inhibitor Saquinavir (sqv) in Complex with Multi-drug Resistant Hiv-1 Protease (L63P/V82T/I84V) (referred to as Act in Paper)
  187. 3ekp: Crystal Structure of The Inhibitor Amprenavir (apv) in Complex with a Multi-drug Resistant Hiv-1 Protease Variant (L10I/G48V/I54V/V64I/V82A)REFER: Flap+ in Citation
  188. 1tsq: Crystal Structure of AP2V Substrate Variant of Nc-p1 Decamer Peptide in Complex with V82A/D25N Hiv-1 Protease Mutant
  189. 1tsu: Crystal Structure of Decamer Ncp1 Substrate Peptide in Complex with Wild-type D25N Hiv-1 Protease Variant
  190. 1tw7: Wide Open 1.3a Structure of a Multi-drug Resistant Hiv-1 Protease Represents a Novel Drug Target
  191. 3dox: X-ray Structure of Hiv-1 Protease in Situ Product Complex
  192. 1u8g: Crystal Structure of a Hiv-1 Protease in Complex with Peptidomimetic Inhibitor Ki2-phe-glu-glu-nh2
  193. 3dk1: Wild Type Hiv-1 Protease with Potent Antiviral Inhibitor Grl-0105a
  194. 3djk: Wild Type Hiv-1 Protease with Potent Antiviral Inhibitor Grl-0255a
  195. 3dcr: X-ray Structure of Hiv-1 Protease and Hydrated Form of Ketomethylene Isostere Inhibitor
  196. 3dck: X-ray Structure of D25N Chemical Analogue of Hiv-1 Protease Complexed with Ketomethylene Isostere Inhibitor
  197. 3d3t: Crystal Structure of Hiv-1 Crf01_ae in Complex with The Substrate P1-p6
  198. 3d20: Crystal Structure of Hiv-1 Mutant I54V and Inhibitor Darunavia
  199. 3d1z: Crystal Structure of Hiv-1 Mutant I54M and Inhibitor Darunavir
  200. 3d1y: Crystal Structure of Hiv-1 Mutant I54V and Inhibitor Saquina
  201. 3d1x: Crystal Structure of Hiv-1 Mutant I54M and Inhibitor Saquinavir
  202. 3cyx: Crystal Structure of Hiv-1 Mutant I50V and Inhibitor Saquinavira
  203. 3cyw: Effect of Flap Mutations on Structure of Hiv-1 Protease and Inhibition by Saquinavir and Darunavir
  204. 3ckt: Hiv-1 Protease in Complex with a Dimethylallyl Decorated Pyrrolidine Based Inhibitor (orthorombic Space Group)
  205. 1vij: Hiv-1 Protease Complexed with The Inhibitor Hoe/bay 793 Hexagonal Form
  206. 1vik: Hiv-1 Protease Complexed with The Inhibitor Hoe/bay 793 Orthorhombic Form
  207. 3bxs: Crystal Structures of Highly Constrained Substrate and Hydrolysis Products Bound to Hiv-1 Protease. Implications for Catalytic Mechanism
  208. 3bxr: Crystal Structures of Highly Constrained Substrate and Hydrolysis Products Bound to Hiv-1 Protease. Implications for Catalytic Mechanism
  209. 3bvb: Cystal Structure of Hiv-1 Active Site Mutant D25N and Inhibitor Darunavir
  210. 3bva: Cystal Structure of Hiv-1 Active Site Mutant D25N and P2-nc Analog Inhibitor
  211. 3bhe: Hiv-1 Protease in Complex with a Three Armed Pyrrolidine Derivative
  212. 3bgc: Hiv-1 Protease in Complex with a Benzyl Decorated Oligoamine
  213. 3bgb: Hiv-1 Protease in Complex with a Isobutyl Decorated Oligoamine
  214. 1w5v: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
  215. 1w5w: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
  216. 1w5x: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
  217. 1w5y: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
  218. 3bc4: I84V Hiv-1 Protease in Complex with a Pyrrolidine Diester
  219. 3b80: Hiv-1 Protease Mutant I54V Complexed with Gem-diol-amine Intermediate Nlltqi
  220. 3b7v: Hiv-1 Protease Complexed with Gem-diol-amine Tetrahedral Intermediate Nlltqi
  221. 3aid: A New Class of Hiv-1 Protease Inhibitor: The Crystallographic Structure, Inhibition and Chemical Synthesis of an Aminimide Peptide Isostere
  222. 3a2o: Crystal Structure of Hiv-1 Protease Complexed with Kni-1689
  223. 2zye: Structure of Hiv-1 Protease in Complex with Potent Inhibitor Kni-272 Determined by Neutron Crystallography
  224. 2zga: Hiv-1 Protease in Complex with a Dimethylallyl Decorated Pyrrolidine Based Inhibitor (hexagonal Space Group)
  225. 2z54: The Influence of I47A Mutation on Reduced Susceptibility to The Protease Inhibitor Lopinavir
  226. 2z4o: Wild Type Hiv-1 Protease with Potent Antiviral Inhibitor Grl-98065
  227. 1xl2: Hiv-1 Protease in Complex with Pyrrolidinmethanamine
  228. 1xl5: Hiv-1 Protease in Complex with Amidhyroxysulfone
  229. 2wl0: Hiv-1 Protease Inhibitors Containing a Tertiary Alcohol in The Transition-state Mimic with Improved Cell-based Antiviral Activity
  230. 2wkz: Hiv-1 Protease Inhibitors Containing a Tertiary Alcohol in The Transition-state Mimic with Improved Cell-based Antiviral Activity
  231. 1ytg: Siv Protease Crystallized with Peptide Product
  232. 1yth: Siv Protease Crystallized with Peptide Product
  233. 1yti: Siv Protease Crystallized with Peptide Product
  234. 1ytj: Siv Protease Crystallized with Peptide Product
  235. 2whh: Hiv-1 Protease Tethered Dimer Q-product Complex along with Nucleophilic Water Molecule
  236. 1z1h: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 3
  237. 1z1r: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 2
  238. 1z8c: Crystal Structure of The Complex of Mutant Hiv-1 Protease (L63P, A71V, V82T, I84V) with a Hydroxyethylamine Peptidomimetic Inhibitor BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE- Glu-phe-nh2
  239. 1zbg: Crystal Structure of a Complex of Mutant Hiv-1 Protease (A71V, V82T, I84V) with a Hydroxyethylamine Peptidomimetic Inhibitor BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE-GLU-PHE-NH2
  240. 1zj7: Crystal Structure of a Complex of Mutant Hiv-1 Protease (A71V, V82T, I84V) with a Hydroxyethylamine Peptidomimetic Inhibitor BOC-PHE-PSI[S-CH(OH)CH2NH]-PHE-GLU-PHE-NH2
  241. 1zlf: Crystal Structure of a Complex of Mutant Hiv-1 Protease (A71V, V82T, I84V) with a Hydroxyethylamine Peptidomimetic Inhibitor
  242. 1zp8: Hiv Protease with Inhibitor Ab-2
  243. 1zpa: Hiv Protease with Scripps Ab-3 Inhibitor
  244. 1zpk: Crystal Structure of The Complex of Mutant Hiv-1 Protease (A71V, V82T, I84V) with a Hydroxyethylamine Peptidomimetic Inhibitor BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE-GLU-PHE-NH2
  245. 1zsf: Crystal Structure of Complex of a Hydroxyethylamine Inhibitor with Hiv-1 Protease at 2.0a Resolution
  246. 1zsr: Crystal Structure of Wild Type Hiv-1 Protease (bru Isolate) with a Hydroxyethylamine Peptidomimetic Inhibitor Boc-phe- PSI[S-CH(OH)CH2NH]-PHE-GLU-PHE-NH2
  247. 1ztz: Crystal Structure of Hiv Protease- Metallacarborane Complex
  248. 2a1e: High Resolution Structure of Hiv-1 Pr with Ts-126
  249. 2a4f: Synthesis and Activity of N-axyl Azacyclic Urea Hiv-1 Protease Inhibitors with High Potency against Multiple Drug Resistant Viral Strains.
  250. 2aid: Structure of a Non-peptide Inhibitor Complexed with Hiv-1 Protease: Developing a Cycle of Structure-based Drug Design
  251. 2aoc: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Substrate Analog P2-nc
  252. 2aod: Crystal Structure Analysis of Hiv-1 Protease with a Substrate Analog P2-nc
  253. 2aoe: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog Ca-p2
  254. 2aof: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog P1-p6
  255. 2aog: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog P2-nc
  256. 2aoh: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog P6-pr
  257. 2aoi: Crystal Structure Analysis of Hiv-1 Protease with a Substrate Analog P1-p6
  258. 2aoj: Crystal Structure Analysis of Hiv-1 Protease with a Substrate Analog P6-pr
  259. 2uy0: Two-carbon-elongated Hiv-1 Protease Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic
  260. 2uxz: Two-carbon-elongated Hiv-1 Protease Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic
  261. 2aqu: Structure of Hiv-1 Protease Bound to Atazanavir
  262. 2avm: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
  263. 2avo: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
  264. 2avq: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
  265. 2avs: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
  266. 2avv: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
  267. 2upj: Hiv-1 Protease Complex with U100313 ([3-[[3-[cyclopropyl [4- Hydroxy-2oxo-6-[1-(phenylmethyl)propyl]-2h-pyran-3-yl] Methyl]phenyl]amino]-3-oxo-propyl]carbamic Acid Tert-butyl Ester)
  268. 2az8: Hiv-1 Protease Nl4-3 in Complex with Inhibitor, Tl-3
  269. 2az9: Hiv-1 Protease Nl4-3 1x Mutant
  270. 2azb: Hiv-1 Protease Nl4-3 3x Mutant in Complex with Inhibitor, Tl-3
  271. 2azc: Hiv-1 Protease Nl4-3 6x Mutant
  272. 2bb9: Structure of Hiv1 Protease and AKC4P_133A Complex.
  273. 2bbb: Structure of Hiv1 Protease and Hh1_173_3a Complex.
  274. 2rkg: Hiv-1 Pr Resistant Mutant + Lpv
  275. 2rkf: Hiv-1 Pr Resistant Mutant + Lpv
  276. 2bpv: Hiv-1 Protease-inhibitor Complex
  277. 2bpw: Hiv-1 Protease-inhibitor Complex
  278. 2bpx: Hiv-1 Protease-inhibitor Complex
  279. 2bpy: Hiv-1 Protease-inhibitor Complex
  280. 2bpz: Hiv-1 Protease-inhibitor Complex
  281. 2bqv: Hiv-1 Protease in Complex with Inhibitor Aha455
  282. 2r43: I50V Hiv-1 Protease in Complex with an Amino Decorated Pyrrolidine-based Inhibitor
  283. 2r3w: I84V Hiv-1 Protease in Complex with a Amino Decorated Pyrrolidine-based Inhibitor
  284. 2r3t: I50V Hiv-1 Protease Mutant in Complex with a Carbamoyl Decorated Pyrrolidine-based Inhibitor
  285. 2r38: I84V Hiv-1 Protease Mutant in Complex with a Carbamoyl Decorated Pyrrolidine-based Inhibitor
  286. 2qnq: Hiv-1 Protease in Complex with a Chloro Decorated Pyrrolidine-based Inhibitor
  287. 2qnp: Hiv-1 Protease in Complex with a Iodo Decorated Pyrrolidine- Based Inhibitor
  288. 2qnn: Hiv-1 Protease in Complex with a Multiple Decorated Pyrrolidine-based Inhibitor
  289. 2qmp: Crystal Structure of Hiv-1 Protease Complexed with Pl-100
  290. 2cej: P1' Extended Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol in The Transition-state Mimicking Scaffold
  291. 2cem: P1' Extended Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol in The Transition-state Mimicking Scaffold
  292. 2cen: P1' Extended Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol in The Transition-state Mimicking Scaffold
  293. 2qhc: The Influence of I47A Mutation on Reduced Susceptibility to The Protease Inhibitor Lopinavir
  294. 2qd8: Hiv-1 Protease Mutant I84V with Potent Antiviral Inhibitor Grl-98065
  295. 2qd7: Hiv-1 Protease Mutant V82A with Potent Antiviral Inhibitor Grl-98065
  296. 2qd6: Hiv-1 Protease Mutant I50V with Potent Antiviral Inhibitor Grl-98065
  297. 2qci: Hiv-1 Protease Mutant D30N with Potent Antiviral Inhibitor Grl-98065
  298. 2qak: Hiv-1 Pr Mutant in Complex with Nelfinavir
  299. 2q64: Hiv-1 Pr Mutant in Complex with Nelfinavir
  300. 2q63: Hiv-1 Pr Mutant in Complex with Nelfinavir
  301. 2pyn: Hiv-1 Pr Mutant in Complex with Nelfinavir
  302. 2pym: Hiv-1 Pr Mutant in Complex with Nelfinavir
  303. 2pwr: Hiv-1 Protease in Complex with a Carbamoyl Decorated Pyrrolidine-based Inhibitor
  304. 2pwc: Hiv-1 Protease in Complex with a Amino Decorated Pyrrolidine-based Inhibitor
  305. 2pqz: Hiv-1 Protease in Complex with a Pyrrolidine-based Inhibitor
  306. 2pc0: Apo Wild-type Hiv Protease in The Open Conformation
  307. 2p3d: Crystal Structure of The Multi-drug Resistant Mutant Subtype F Hiv Protease Complexed with Tl-3 Inhibitor
  308. 2p3c: Crystal Structure of The Subtype F Wild Type Hiv Protease Complexed with Tl-3 Inhibitor
  309. 2p3b: Crystal Structure of The Subtype B Wild Type Hiv Protease Complexed with Tl-3 Inhibitor
  310. 2p3a: Crystal Structure of The Multi-drug Resistant Mutant Subtype B Hiv Protease Complexed with Tl-3 Inhibitor
  311. 6y9z: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,9)
  312. 6y9y: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-7,13)
  313. 6y9x: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,7)
  314. 6y9w: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,8)
  315. 6y9v: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-8,13)
  316. 2o40: Crystal Structure of a Chemically Synthesized 203 Amino Acid 'covalent Dimer' Hiv-1 Protease Molecule
  317. 6b3h: Crystal Structure of Hiv Protease Complexed with N-(2-(2-((6r,9s)-2,2- Dioxido-2-thia-1,7-diazabicyclo[4.3.1]decan-9-yl)ethyl)-3- Fluorophenyl)-3,3-bis(4-fluorophenyl)propanamide
  318. 6b3g: Crystal Structure of Hiv Protease Complexed with N-(3-fluoro-2-(2- ((2s,6s)-6-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3- Bis(4-fluorophenyl)propanamide
  319. 6b3f: Crystal Structure of Hiv Protease Complexed with N-(3-fluoro-2-(2- ((2s,5s)-5-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3- Bis(4-fluorophenyl)propanamide
  320. 6b3c: Crystal Structure of Hiv Protease Complexed with N-(3-fluoro-2-(2- ((2s,6r)-6-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3- Bis(4-fluorophenyl)propanamide
  321. 6b38: Crystal Structure of Hiv Protease Complexed with N-(3-fluoro-2-(2- ((2s,6r)-6-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3- Bis(4-fluorophenyl)propanamide
  322. 6b36: Crystal Structure of Hiv Protease Complexed with (s)-n-(3-fluoro-2-(2- (1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3-bis(4- Fluorophenyl)propanamide
  323. 2nxm: Structure of Hiv-1 Protease D25N Complexed with The Rt-rh Analogue Peptide Gly-ala-gln-thr-phe*tyr-val-asp-gly-ala
  324. 2nxl: Structure of Hiv-1 Protease D25N Complexed with The Rt-rh Analogue Peptide Gly-ala-glu-val-phe*tyr-val-asp-gly-ala
  325. 2nxd: Structure of Hiv-1 Protease D25N Complexed with Rt-rh Analogue Peptide Gly-ala-asp-ile-phe*tyr-leu-asp-gly-ala
  326. 2nph: Crystal Structure of Hiv1 Protease in Situ Product Complex
  327. 2nnp: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Inhibitor Saquinavir
  328. 2nnk: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Inhibitor Saquinavir
  329. 2nmz: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Inhibitor Saquinavir
  330. 2nmy: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Inhibitor Saquinavir
  331. 2f3k: Substrate Envelope and Drug Resistance: Crystal Structure of R01 in Complex with Wild-type Hiv-1 Protease
  332. 2f80: Hiv-1 Protease Mutant D30N Complexed with Inhibitor Tmc114
  333. 2f81: Hiv-1 Protease Mutant L90M Complexed with Inhibitor Tmc114
  334. 2f8g: Hiv-1 Protease Mutant I50V Complexed with Inhibitor Tmc114
  335. 2fdd: Crystal Structure of Hiv Protease D545701 Bound with Gw0385
  336. 2fde: Wild Type Hiv Protease Bound with Gw0385
  337. 2fgu: X-ray Crystal Structure of Hiv-1 Protease T80S Variant in Complex with The Inhibitor Saquinavir Used to Explore The Role of Invariant Thr80 in Hiv-1 Protease Structure, Function, and Viral Infectivity.
  338. 2fgv: X-ray Crystal Structure of Hiv-1 Protease T80N Variant in Complex with The Inhibitor Saquinavir Used to Explore The Role of Invariant Thr80 in Hiv-1 Protease Structure, Function, and Viral Infectivity.
  339. 2fiv: Crystal Structure of Feline Immunodeficiency Virus Protease Complexed with a Substrate
  340. 2fns: Crystal Structure of Wild-type Inactive (D25N) Hiv-1 Protease Complexed with Wild-type Hiv-1 Nc-p1 Substrate.
  341. 2fnt: Crystal Structure of a Drug-resistant (V82A) Inactive (D25N) Hiv-1 Protease Complexed with AP2V Variant of Hiv-1 Nc-p1 Substrate.
  342. 2fxd: X-ray Crystal Structure of Hiv-1 Protease Irm Mutant Complexed with Atazanavir (bms-232632)
  343. 2fxe: X-ray Crystal Structure of Hiv-1 Protease Crm Mutant Complexed with Atazanavir (bms-232632)
  344. 2g69: Structure of Unliganded Hiv-1 Protease F53L Mutant
  345. 5yrs: X-ray Snapshot of Hiv-1 Protease in Action: Observation of Tetrahedral Intermediate and Its Sihb with Catalytic Aspartate
  346. 5yoj: Structure of A17 Hiv-1 Protease in Complex with Inhibitor Kni-1657
  347. 2hah: The Structure of Fiv 12s Protease in Complex with Tl-3
  348. 2hb2: Structure of Hiv Protease 6x Mutant in Apo Form
  349. 2hb4: Structure of Hiv Protease Nl4-3 in an Unliganded State
  350. 2hc0: Structure of Hiv Protease 6x Mutant in Complex with Ab-2.
  351. 2hs1: Ultra-high Resolution X-ray Crystal Structure of Hiv-1 Protease V32I Mutant with Tmc114 (darunavir) Inhibitor
  352. 2hs2: Crystal Structure of M46L Mutant of Hiv-1 Protease Complexed with Tmc114 (darunavir)
  353. 2i4d: Crystal Structure of Wt Hiv-1 Protease with Gs-8373
  354. 2i4u: Hiv-1 Protease with Tmc-126
  355. 2i4v: Hiv-1 Protease I84V, L90M with Tmc126
  356. 2i4w: Hiv-1 Protease Wt with Gs-8374
  357. 2i4x: Hiv-1 Protease I84V, L90M with Gs-8374
  358. 2idw: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Potent Non-peptide Inhibitor (uic-94017)
  359. 2ien: Crystal Structure Analysis of Hiv-1 Protease with a Potent Non-peptide Inhibitor (uic-94017)
  360. 2ieo: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Potent Non-peptide Inhibitor (uic-94017)
  361. 2jo0: The Solution Structure of The Monomeric Species of The C Terminal Domain of The Ca Protein of Hiv-1
  362. 3oy4: Crystal Structure of Hiv-1 L76V Protease in Complex with The Protease Inhibitor Darunavir.
  363. 3hau: Crystal Structure of Chemically Synthesized Hiv-1 Protease with Reduced Isostere Mvt-101 Inhibitor
  364. 3haw: Crystal Structure of [l-ala51/51']hiv-1 Protease with Reduced Isostere Mvt-101 Inhibitor
  365. 3hzc: Crystal Structure of a Chemically Synthesized 203 Amino Acid 'covalent Dimer' [gly51;aib51']hiv-1 Protease Molecule Complexed with Mvt-101 Reduced Isostere Inhibitor
  366. 3i2l: Crystal Structure of a Chemically Synthesized [allo-ile50/50']hiv-1 Protease Molecule Complexed with Mvt-101 Reduced Isostere Inhibitor
  367. 3iaw: Crystal Structure of a Chemically Synthesized 203 Amino Acid 'covalent Dimer' [gly51;aib51']hiv-1 Protease Molecule Complexed with Mvt-101 Reduced Isostere Inhibitor at 1.6 a Resolution
  368. 3ka2: Crystal Structure of Chemically Synthesized 203 Amino Acid 'covalent Dimer' [l-ala;gly51']hiv-1 Protease Molecule Complexed with Mvt-101 Reduced Isostere Inhibitor at 1.4 a Resolution
  369. 3mws: Crystal Structure of Group N Hiv-1 Protease
  370. 3pwm: Hiv-1 Protease Mutant L76V with Darunavir
  371. 3pwr: Hiv-1 Protease Mutant L76V Complexed with Saquinavir
  372. 3qin: Crystal Structure of Hiv-1 Rnase H P15 with Engineered E. Coli Loop and Pyrimidinol Carboxylic Acid Inhibitor
  373. 3qio: Crystal Structure of Hiv-1 Rnase H with Engineered E. Coli Loop and N- Hydroxy Quinazolinedione Inhibitor
  374. 3qip: Structure of Hiv-1 Reverse Transcriptase in Complex with an Rnase H Inhibitor and Nevirapine
  375. 6p9b: Hiv-1 Protease Multiple Drug Resistant Mutant PRS5B with Amprenavir
  376. 6p9a: Hiv-1 Protease Multiple Mutant PRS5B with Darunavir
  377. 3hlo: Crystal Structure of Chemically Synthesized 'covalent Dimer' [gly51/d- Ala51']hiv-1 Protease
  378. 3ia9: Crystal Structure of a Chemically Synthesized [D25N]HIV-1 Protease Molecule Complexed with Mvt-101 Reduced Isostere Inhibitor
  379. 3ndt: Hiv-1 Protease Saquinavir:ritonavir 1:1 Complex Structure
  380. 3ndu: Hiv-1 Protease Saquinavir:ritonavir 1:5 Complex Structure
  381. 3ndw: Hiv-1 Protease Saquinavir:ritonavir 1:15 Complex Structure
  382. 3ndx: Hiv-1 Protease Saquinavir:ritonavir 1:50 Complex Structure
  383. 6ujx: Hiv-1 Wild-type Reverse Transcriptase-dna Complex with (-)-ftc-tp
  384. 3gi0: Crystal Structure of a Chemically Synthesized 203 Amino Acid 'covalent Dimer' [l-ala51,d-ala51'] Hiv-1 Protease Molecule Complexed with Jg- 365 Inhibitor
  385. 3st5: Crystal Structure of Wild-type Hiv-1 Protease with C3-substituted Hexahydrocyclopentafuranyl Urethane as P2-ligand, Grl-0489a
  386. 3nls: Crystal Structure of Hiv-1 Protease in Complex with Kni-10772
  387. 3oxv: Crystal Structure of Hiv-1 I50V, A71 Protease in Complex with The Protease Inhibitor Amprenavir.
  388. 3oxw: Crystal Structure of Hiv-1 I50V, A71V Protease in Complex with The Protease Inhibitor Darunavir
  389. 3oxx: Crystal Structure of Hiv-1 I50V, A71V Protease in Complex with The Protease Inhibitor Atazanavir
  390. 3th9: Crystal Structure of Hiv-1 Protease Mutant Q7K V32I L63I with a Cyclic Sulfonamide Inhibitor
  391. 3so9: Darunavir in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
  392. 3spk: Tipranavir in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
  393. 3tam: Crystal Structure of Hiv-1 Reverse Transcriptase (K103N Mutant) in Complex with Inhibitor M06
  394. 3nwq: X-ray Structure of Ester Chemical Analogue [o-ile50,o-ile50']hiv-1 Protease Complexed with Mvt-101
  395. 3nwx: X-ray Structure of Ester Chemical Analogue [o-ile50,o-ile50']hiv-1 Protease Complexed with Kvs-1 Inhibitor
  396. 3nxe: X-ray Structure of Ester Chemical Analogue 'covalent Dimer' [ile50,o- Ile50']hiv-1 Protease Complexed with Mvt-101 Inhibitor
  397. 3nxn: X-ray Structure of Ester Chemical Analogue 'covalent Dimer' [ile50,o- Ile50']hiv-1 Protease Complexed with Kvs-1 Inhibitor
  398. 3nyg: X-ray Structure of Ester Chemical Analogue [o-gly51,o-gly51']hiv-1 Protease Complexed with Mvt-101 Inhibitor
  399. 2xye: Hiv-1 Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic and Various P2 and P1 Prime Substituents
  400. 2xyf: Hiv-1 Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic and Various P2 and P1 Prime Substituents
  401. 3psu: Hiv-1 Protease in Complex with an Isobutyl Decorated Oligoamine (symmetric Binding Mode)
  402. 3qaa: Hiv-1 Wild Type Protease with a Substituted Bis-tetrahydrofuran Inhibitor, Grl-044-10a
  403. 3qbf: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
  404. 3u7s: Hiv Pr Drug Resistant Patient's Variant in Complex with Darunavir
  405. 3qih: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Novel Inhibitor
  406. 6prf: Hiv-1 Protease Multiple Drug Resistant Clinical Isolate Mutant Pr20 with Grl-14213a
  407. 3qn8: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Novel Inhibitor
  408. 3qp0: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Novel Inhibitor
  409. 3qpj: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
  410. 3qrm: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
  411. 3qro: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
  412. 3qrs: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
  413. 3s43: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Amprenavir
  414. 3s53: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Darunavir in Space Group P212121
  415. 3s54: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Darunavir in Space Group P21212
  416. 3s56: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Saquinavir
  417. 6o9e: Structure of Hiv-1 Reverse Transcriptase in Complex with Dna and Indopy-1
  418. 4dfg: Crystal Structure of Wild-type Hiv-1 Protease with Cyclopentyltetrahydro- Furanyl Urethanes as P2-ligand, Grl-0249a
  419. 3uhl: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 in Complex with P2-nc Substrate Analog
  420. 3tkg: Crystal Structure of Hiv Model Protease Precursor/saquinavir Complex
  421. 3tkw: Crystal Structure of Hiv Protease Model Precursor/darunavir Complex
  422. 3tl9: Crystal Structure of Hiv Protease Model Precursor/saquinavir Complex
  423. 4a6b: Stereoselective Synthesis, X-ray Analysis, and Biological Evaluation of a New Class of Lactam Based Hiv-1 Protease Inhibitors
  424. 4a6c: Stereoselective Synthesis, X-ray Analysis, and Biological Evaluation of a New Class of Lactam Based Hiv-1 Protease Inhibitors
  425. 4ep2: Crystal Structure of Inactive Single Chain Wild-type Hiv-1 Protease in Complex with The Substrate Rt-rh
  426. 4ep3: Crystal Structure of Inactive Single Chain Wild-type Hiv-1 Protease in Complex with The Substrate Ca-p2
  427. 4epj: Crystal Structure of Inactive Single Chain Wild-type Hiv-1 Protease in Complex with The Substrate P2-nc
  428. 4eq0: Crystal Structure of Inactive Single Chain Variant of Hiv-1 Protease in Complex with The Substrate P2-nc
  429. 4eqj: Crystal Structure of Inactive Single Chain Variant of Hiv-1 Protease in Complex with The Substrate Rt-rh
  430. 3t3c: Structure of Hiv Pr Resistant Patient Derived Mutant (comprising 22 Mutations) in Complex with Drv
  431. 4fe6: Crystal Structure of Hiv-1 Protease in Complex with an Enamino- Oxindole Inhibitor
  432. 3tof: Hiv-1 Protease - Epoxydic Inhibitor Complex (ph 6 - Orthorombic Crystal Form P212121)
  433. 3tog: Hiv-1 Protease - Epoxydic Inhibitor Complex (ph 9 - Monoclinic Crystal Form P21)
  434. 3toh: Hiv-1 Protease - Epoxydic Inhibitor Complex (ph 9 - Orthorombic Crystal Form P212121)
  435. 3t11: Dimeric Inhibitor of Hiv-1 Protease.
  436. 3ttp: Structure of Multiresistant Hiv-1 Protease in Complex with Darunavir
  437. 4fae: Substrate P2/nc in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
  438. 4faf: Substrate Ca/p2 in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
  439. 6ixd: X-ray Crystal Structure of Bpi-11 Hiv-1 Protease Complex
  440. 4fl8: Hiv-1 Protease Complexed with Gem-diol-amine Tetrahedral Intermediate
  441. 4flg: Hiv-1 Protease Mutant I47V Complexed with Reaction Intermediate
  442. 4fm6: Hiv-1 Protease Mutant V32I Complexed with Reaction Intermediate
  443. 3vf5: Crystal Structure of Hiv-1 Protease Mutant I47V with Novel P1'-ligands Grl-02031
  444. 3vf7: Crystal Structure of Hiv-1 Protease Mutant L76V with Novel P1'-ligands Grl-02031
  445. 3vfa: Crystal Structure of Hiv-1 Protease Mutant V82A with Novel P1'-ligands Grl-02031
  446. 3vfb: Crystal Structure of Hiv-1 Protease Mutant N88D with Novel P1'-ligands Grl-02031
  447. 4a4q: Stereoselective Synthesis, X-ray Analysis, and Biological Evaluation of a New Class of Lactam Based Hiv-1 Protease Inhibitors
  448. 2fmb: Eiav Protease Complexed with an Inhibitor Lp-130
  449. 4b3o: Structures of Hiv-1 Rt and Rna-dna Complex Reveal a Unique Rt Conformation and Substrate Interface
  450. 4b3p: Structures of Hiv-1 Rt and Rna-dna Complex Reveal a Unique Rt Conformation and Substrate Interface
  451. 4b3q: Structures of Hiv-1 Rt and Rna-dna Complex Reveal a Unique Rt Conformation and Substrate Interface
  452. 4i2p: Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with Rilpivirine (tmc278) Based Analogue
  453. 4i2q: Crystal Structure of K103N/Y181C Mutant of Hiv-1 Reverse Transcriptase in Complex with Rilpivirine (tmc278) Analogue
  454. 6hak: Crystal Structure of Hiv-1 Reverse Transcriptase (rt) in Complex with a Double Stranded Rna Represents The Rt Transcription Initiation Complex Prior to Nucleotide Incorporation
  455. 4ej8: Apo Hiv Protease (pr) Dimer in Closed Form with Fragment 1f1 in The Outside/top of Flap
  456. 4ejd: Hiv Protease (pr) Dimer in Closed Form with Pepstatin in Active Site and Fragment 1f1 in The Outside/top of Flap
  457. 4ejk: Hiv Protease (pr) Dimer in Closed Form with Pepstatin in Active Site and Fragment 1f1-n in The Outside/top of Flap
  458. 4ejl: Apo Hiv Protease (pr) Dimer in Closed Form with Fragment 1f1-n in The Outside/top of Flap
  459. 4gvm: Hiv-1 Integrase Catalytic Core Domain A128T Mutant Complexed with Allosteric Inhibitor
  460. 4gw6: Hiv-1 Integrase Catalytic Core Domain Complexed with Allosteric Inhibitor
  461. 4id1: Hiv-1 Integrase Catalytic Core Domain Complexed with Allosteric Inhibitor
  462. 4f73: Crystal Structure of Active Hiv-1 Protease in Complex with The N Terminal Product of Ca-p2 Cleavage Site
  463. 4f74: Crystal Structure of Active Hiv-1 Protease in Complex with The N Terminal Product of The Substrate Ma-ca.
  464. 4f75: Crystal Structure of Active Hiv-1 Protease in Complex with The N Terminal Product of The Substrate Rh-in
  465. 4f76: Crystal Structure of The Active Hiv-1 Protease in Complex with The Products of P1-p6 Substrate
  466. 4j54: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 with The Potent Antiviral Inhibitor Grl-0519a
  467. 4j55: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 with The Potent Antiviral Inhibitor Grl-02031
  468. 4j5j: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 in Complex with Amprenavir
  469. 4hla: Crystal Structure of Wild Type Hiv-1 Protease in Complex with Darunavir
  470. 4i8w: Crystal Structure of Wild Type Hiv-1 Protease in Complex with Non- Peptidic Inhibitor, Grl007
  471. 4i8z: Crystal Structure of Wild Type Hiv-1 Protease in Complex with Non- Peptidic Inhibitor, Grl008
  472. 4jec: Joint Neutron and X-ray Structure of Per-deuterated Hiv-1 Protease in Complex with Clinical Inhibitor Amprenavir
  473. 4gb2: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Bicyclic Pyrrolidine Inhibitor
  474. 3zps: Design and Synthesis of P1-p3 Macrocyclic Tertiary Alcohol Comprising Hiv-1 Protease Inhibitors
  475. 3zpt: Design and Synthesis of P1-p3 Macrocyclic Tertiary Alcohol Comprising Hiv-1 Protease Inhibitors
  476. 3zpu: Design and Synthesis of P1-p3 Macrocyclic Tertiary Alcohol Comprising Hiv-1 Protease Inhibitors
  477. 6cdl: Hiv-1 Wild Type Protease with Grl-03214a, 6-5-5-ring Fused Umbrella- like Tetrahydropyranofuran as The P2-ligand, a Cyclopropylaminobenzothiazole as The P2'-ligand and 3,5- Difluorophenylmethyl as The P1-ligand
  478. 4gye: Mdr 769 Hiv-1 Protease in Complex with Reduced P1F
  479. 4gzf: Multi-drug Resistant Hiv-1 Protease 769 Variant with Reduced Lrf Peptide
  480. 4hdb: Crystal Structure of Hiv-1 Protease Mutants D30N Complexed with Inhibitor Grl-0519
  481. 4hdf: Crystal Structure of Hiv-1 Protease Mutants V82A Complexed with Inhibitor Grl-0519
  482. 4hdp: Crystal Structure of Hiv-1 Protease Mutants I50V Complexed with Inhibitor Grl-0519
  483. 4he9: Crystal Structure of Hiv-1 Protease Mutants I54M Complexed with Inhibitor Grl-0519
  484. 4heg: Crystal Structure of Hiv-1 Protease Mutants R8Q Complexed with Inhibitor Grl-0519
  485. 4jmu: Crystal Structure of Hiv Matrix Residues 1-111 in Complex with Inhibitor
  486. 4k4p: Tl-3 Inhibited TRP6ALA Hiv Protease
  487. 4k4q: Tl-3 Inhibited TRP6ALA Hiv Protease with 3-bromo-2,6-dimethoxybenzoic Acid Bound in Flap Site
  488. 4k4r: Tl-3 Inhibited TRP6ALA Hiv Protease with 1-bromo-2-napthoic Acid Bound in Exosite
  489. 4kb9: Crystal Structure of Wild-type Hiv-1 Protease with Novel Tricyclic P2- Ligands Grl-0739a
  490. 4m8x: Gs-8374, a Novel Phosphonate-containing Inhibitor of Hiv-1 Protease, Effectively Inhibits Hiv Pr Mutants with Amino Acid Insertions
  491. 4m8y: Gs-8374, a Novel Phosphonate-containing Inhibitor of Hiv-1 Protease, Effectively Inhibits Hiv Pr Mutants with Amino Acid Insertions
  492. 4mc1: Hiv Protease in Complex with SA526P
  493. 4mc2: Hiv Protease in Complex with SA525P
  494. 4mc6: Hiv Protease in Complex with Sa499
  495. 4mc9: Hiv Protease in Complex with Aa74
  496. 4qgi: X-ray Crystal Structure of Hiv-1 Protease Variant G48T/L89M in Complex with Saquinavir
  497. 4qj2: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with Wt P1-p6 Substrate
  498. 4qj6: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with P1-p6 Substrate Variant (L449F)
  499. 4qj7: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with P1-p6 Substrate Variant (R452S)
  500. 4qj8: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with P1-p6 Substrate Variant (P453L)
  501. 4qj9: Crystal Structure of Inactive Hiv-1 Protease in Complex with P1-p6 Substrate Variant (R452S)
  502. 4qja: Crystal Structure of Inactive Hiv-1 Protease in Complex with P1-p6 Substrate Variant (P453L)
  503. 4qlh: Crystal Structure of Drug Resistant V82S/V1082S Hiv-1 Protease
  504. 5vj3: Hiv Protease (pr) in Open Form with Mg2+ in Active Site and Hive-9 in Eye Site
  505. 4u8w: Hiv-1 Wild Type Protease with Grl-050-10a (a Gem-difluoro-bis- Tetrahydrofuran as P2-ligand)
  506. 5vea: Hiv Protease (pr) with Tl-3 in Active Site and 4-methylbenzene-1,2- Diamine in Exosite
  507. 5vck: Hiv Protease (pr) with Tl-3 in The Active Site and (z)-n-(thiazol-2- Yl)-n'-tosylcarbamimidate in The Exosite
  508. 4obd: Crystal Structure of Nelfinavir-resistant, Inactive Hiv-1 Protease (D30N/N88D) in Complex with The P1-p6 Substrate Variant (L449F/S451N)
  509. 4obf: Crystal Structure of Nelfinavir-resistant, Inactive Hiv-1 Protease Variant (D30N/N88D) in Complex with The P1-p6 Substrate Variant (S451N)
  510. 4obg: Crystal Structure of Nelfinavir-resistant, Inactive Hiv-1 Protease (D30N/N88D) in Complex with The P1-p6 Substrate.
  511. 4obh: Crystal Structure of Inactive Hiv-1 Protease in Complex with The P1-p6 Substrate Variant (L449F)
  512. 4obj: Crystal Structure of Inactive Hiv-1 Protease in Complex with The P1-p6 Substrate Variant (S451N)
  513. 4obk: Crystal Structure of Inactive Hiv-1 Protease in Complex with The P1-p6 Substrate Variant (L449F/S451N)
  514. 4we1: Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with 5-(2- (2-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)ethoxy)phenoxy)-2- Naphthonitrile (jlj600)
  515. 4coe: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  516. 4cp7: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  517. 4cpq: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  518. 4cpr: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  519. 4cps: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  520. 4cpt: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  521. 4cpu: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  522. 4cpw: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  523. 4cpx: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
  524. 5tw3: Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with 5-(2- (2-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)ethoxy)-4-fluorophenoxy)- 7-fluoro-2-naphthonitrile (jlj636), a Non-nucleoside Inhibitor
  525. 5tuq: Crystal Structure of a 6-cyclohexylmethyl-3-hydroxypyrimidine-2,4- Dione Inhibitor in Complex with Hiv Reverse Transcriptase
  526. 5ter: Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with 5- Chloro-7-(2-(2-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl)ethoxy) Phenoxy)-8-methyl-2-naphthonitrile (jlj651), a Non-nucleoside Inhibitor
  527. 5e5k: Joint X-ray/neutron Structure of Hiv-1 Protease Triple Mutant (V32I, I47V,V82I) with Darunavir at Ph 4.3
  528. 5c42: Crystal Structure of Hiv-1 Reverse Transcriptase (K101P) Variant in Complex with 8-(2-(2-(2,4-dioxo-3,4-dihydropyrimidin-1(2h)-yl) Ethoxy)phenoxy)indolizine-2-carbonitrile (jlj555), a Non-nucleoside Inhibitor
  529. 5c25: Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with 6- ((4-((4-cyanophenyl)amino)-1,3,5-triazin-2-yl)amino)-5,7-dimethyl-2- Naphthonitrile (jlj639), a Non-nucleoside Inhibitor
  530. 5c24: Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with 7- ((4-((4-cyanophenyl)amino)-1,3,5-triazin-2-yl)amino)-6,8- Dimethylindolizine-2-carbonitrile (jlj605), a Non-nucleoside Inhibitor
  531. 5bs4: Hiv-1 Wild Type Protease with Grl-047-11a (a Methylamine Bis- Tetrahydrofuran P2-ligand, 4-amino Sulfonamide Derivative)
  532. 5bry: Hiv-1 Wild Type Protease with Grl-011-11a (a Methylamine Bis- Tetrahydrofuran P2-ligand, Sulfonamide Isostere Derivate)
  533. 4q1w: Mutations outside The Active Site of Hiv-1 Protease Alter Enzyme Structure and Dynamic Ensemble of The Active Site to Confer Drug Resistance
  534. 4q1x: Mutations outside The Active Site of Hiv-1 Protease Alter Enzyme Structure and Dynamic Ensemble of The Active Site to Confer Drug Resistance
  535. 4q1y: Mutations outside The Active Site of Hiv-1 Protease Alter Enzyme Structure and Dynamic Ensemble of The Active Site to Confer Drug Resistance
  536. 5ah7: Disubstituted Bis-thf Moieties as New P2 Ligands in Non-peptidal Hiv-1 Protease Inhibitors (ii)
  537. 4zls: Hiv-1 Wild Type Protease with Grl-096-13a (a Boc-derivative P2-ligand, 3,-5-dimethylbiphenyl P1-ligand)
  538. 4zip: Hiv-1 Wild Type Protease with Grl-0648a (a Isophthalamide-derived P2- Ligand)
  539. 4q5m: D30N Tethered Hiv-1 Protease Dimer/saquinavir Complex
  540. 4yhq: Crystal Structure of Multidrug Resistant Clinical Isolate Pr20 with Grl-5010a
  541. 4ye3: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 with Inhibitor Grl-4410a
  542. 5agz: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
  543. 5ah6: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
  544. 5ah8: Disubstituted Bis-thf Moieties as New P2 Ligands in Non-peptidal Hiv-1 Protease Inhibitors (ii)
  545. 5ah9: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
  546. 5aha: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
  547. 5ahb: Disubstituted Bis-thf Moieties as New P2 Ligands in Non-peptidal Hiv-1 Protease Inhibitors (ii)
  548. 5ahc: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
  549. 7ahx: Hiv-1 Reverse Transcriptase Complex with Dna and D-aspartate Tenofovir with Bound Manganese
  550. 7aid: Hiv-1 Reverse Transcriptase Complex with Dna and D-aspartate Tenofovir
  551. 7aif: Hiv-1 Reverse Transcriptase Complex with Dna and L-glutamate Tenofovir with Bound Manganese
  552. 7aig: Hiv-1 Reverse Transcriptase Complex with Dna and L-glutamate Tenofovir
  553. 7aii: Hiv-1 Reverse Transcriptase Complex with Dna and L-methionine Tenofovir with Bound Manganese
  554. 7aij: Hiv-1 Reverse Transcriptase Complex with Dna and L-methionine Tenofovir
  555. 6vug: Diabody Bound to a Reverse Transcriptase Aptamer Complex
  556. 7n6t: Crystal Structure of Inhibitor-free Hiv-1 Prs17 Revertant Mutant Prs17 V48G
  557. 7n6v: Crystal Structure of Hiv-1 Protease Multiple Mutants Prs17 with Revertant Mutation V48G Bound to Inhibitor Amprenavir
  558. 7n6x: Crystal Structure of Hiv-1 Protease Multiple Mutants Prs17 Bound to Inhibitor Amprenavir
  559. 7oxq: Crystal Structure of Hiv-1 Reverse Transcriptase with a Double Stranded Dna in Complex with Fragment 048 at The Transient P-pocket.
  560. 7oz2: Crystal Structure of Hiv-1 Reverse Transcriptase with a Double Stranded Dna Showing a Transient P-pocket
  561. 7oz5: Crystal Structure of Hiv-1 Reverse Transcriptase with a Double Stranded Dna in Complex with Fragment 166 at The Transient P-pocket.
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