Enzyme classes: General information:
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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:
- 1a30: Hiv-1 Protease Complexed with a Tripeptide Inhibitor
- 1a8g: Hiv-1 Protease in Complex with Sdz283-910
- 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
- 1a94: Structural Basis for Specificity of Retroviral Proteases
- 1aid: Structure of a Non-peptide Inhibitor Complexed with Hiv-1 Protease: Developing a Cycle of Structure-based Drug Design
- 1ajv: Hiv-1 Protease in Complex with The Cyclic Sulfamide Inhibitor Aha006
- 1ajx: Hiv-1 Protease in Complex with The Cyclic Urea Inhibitor Aha001
- 1axa: Active-site Mobility in Human Immunodeficiency Virus Type 1 Protease as Demonstrated by Crystal Structure of A28S Mutant
- 1az5: Unliganded Siv Protease Structure in an "open" Conformation
- 1b11: Structure of Feline Immunodeficiency Virus Protease Complexed with Tl-3-093
- 1b6j: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 1
- 1b6k: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 5
- 1b6l: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 4
- 1b6m: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 6
- 1b6p: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 7
- 1bdl: Hiv-1 (2:31-37) Protease Complexed with Inhibitor Sb203386
- 1bdq: Hiv-1 (2:31-37, 47, 82) Protease Complexed with Inhibitor Sb203386
- 1bdr: Hiv-1 (2: 31, 33-37) Protease Complexed with Inhibitor Sb203386
- 1bv7: Counteracting Hiv-1 Protease Drug Resistance: Structural Analysis of Mutant Proteases Complexed with Xv638 and Sd146, Cyclic Urea Amides with Broad Specificities
- 1bv9: Hiv-1 Protease (I84V) Complexed with Xv638 of Dupont Pharmaceuticals
- 1bve: Hiv-1 Protease-dmp323 Complex in Solution, Nmr, 28 Structures
- 1bvg: Hiv-1 Protease-dmp323 Complex in Solution, Nmr Minimized Average Structure
- 1bwa: Hiv-1 Protease (V82F/I84V) Double Mutant Complexed with Xv638 of Dupont Pharmaceuticals
- 1bwb: Hiv-1 Protease (V82F/I84V) Double Mutant Complexed with Sd146 of Dupont Pharmaceuticals
- 1d4h: Hiv-1 Protease in Complex with The Inhibitor Bea435
- 1d4i: Hiv-1 Protease in Complex with The Inhibitor Bea425
- 1d4j: Hiv-1 Protease in Complex with The Inhibitor Msl370
- 1d4k: Hiv-1 Protease Complexed with a Macrocyclic Peptidomimetic Inhibitor
- 1d4l: Hiv-1 Protease Complexed with a Macrocyclic Peptidomimetic Inhibitor
- 1d4s: Hiv-1 Protease V82F/I84V Double Mutant/tipranavir Complex
- 1d4y: Hiv-1 Protease Triple Mutant/tipranavir Complex
- 1daz: Structural and Kinetic Analysis of Drug Resistant Mutants of Hiv-1 Protease
- 1dmp: Structure of Hiv-1 Protease Complex
- 1dw6: Structural and Kinetic Analysis of Drug Resistant Mutants of Hiv-1 Protease
- 1ebk: Structural and Kinetic Analysis of Drug Resistant Mutants of Hiv-1 Protease
- 1ebw: Hiv-1 Protease in Complex with The Inhibitor Bea322
- 1eby: Hiv-1 Protease in Complex with The Inhibitor Bea369
- 1ebz: Hiv-1 Protease in Complex with The Inhibitor Bea388
- 1ec0: Hiv-1 Protease in Complex with The Inhibitor Bea403
- 1ec1: Hiv-1 Protease in Complex with The Inhibitor Bea409
- 1ec2: Hiv-1 Protease in Complex with The Inhibitor Bea428
- 1ec3: Hiv-1 Protease in Complex with The Inhibitor Msa367
- 1f7a: How Does a Symmetric Dimer Recognize an Asymmetric Substrate? a Substrate Complex of Hiv-1 Protease.
- 1fej: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
- 1ff0: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes.
- 1fff: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease : High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes.
- 1ffi: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
- 1fg6: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
- 1fg8: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
- 1fgc: Structural Implications of Drug Resistant Mutants of Hiv-1 Protease: High Resolution Crystal Structures of The Mutant Protease/substrate Analog Complexes
- 1fiv: Structure of an Inhibitor Complex of Proteinase from Feline Immunodeficiency Virus
- 1fmb: Eiav Protease Complexed with The Inhibitor Hby-793
- 1fqx: Crystal Structure of The Complex of Hiv-1 Protease with a Peptidomimetic Inhibitor
- 1g2k: Hiv-1 Protease with Cyclic Sulfamide Inhibitor, Aha047
- 1g35: Crystal Structure of Hiv-1 Protease in Complex with Inhibitor, Aha024
- 1g6l: 1.9a Crystal Structure of Tethered Hiv-1 Protease
- 1hpo: Hiv-1 Protease Triple Mutant/u103265 Complex
- 1hvh: Nonpeptide Cyclic Cyanoguanidines as Hiv Protease Inhibitors
- 1hwr: Molecular Recognition of Cyclic Urea Hiv Protease Inhibitors
- 1hxb: Hiv-1 Proteinase Complexed with Ro 31-8959
- 1hxw: Hiv-1 Protease Dimer Complexed with A-84538
- 1iiq: Crystal Structure of Hiv-1 Protease Complexed with a Hydroxyethylamine Peptidomimetic Inhibitor
- 1izh: Inhibitor of Hiv Protease with Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants
- 1izi: Inhibitor of Hiv Protease with Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants
- 1jld: Potent Hiv Protease Inhibitors Containing a Novel (hydroxyethyl)amide Isostere
- 1k1t: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
- 1k1u: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
- 1k2b: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
- 1k2c: Combining Mutations in Hiv-1 Protease to Understand Mechanisms of Resistance
- 1k6c: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
- 1k6p: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
- 1k6t: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
- 1k6v: Lack of Synergy for Inhibitors Targeting a Multi-drug Resistant Hiv-1 Protease
- 7upj: Hiv-1 Protease/u101935 Complex
- 6upj: Hiv-2 Protease/u99294 Complex
- 6fiv: Structural Studies of Hiv and Fiv Proteases Complexed with an Efficient Inhibitor of Fiv Pr
- 5upj: Hiv-2 Protease/u99283 Complex
- 5fiv: Structural Studies of Hiv and Fiv Proteases Complexed with an Efficient Inhibitor of Fiv Pr
- 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
- 4fiv: Fiv Protease Complexed with an Inhibitor Lp-130
- 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]
- 3tlh: Structural Studies of Hiv and Fiv Proteases Complexed Withan Efficient Inhibitor of Fiv Pr
- 1kj4: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
- 1kj7: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
- 1kjf: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
- 1kjg: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
- 1kjh: Substrate Shape Determines Specificity of Recognition Recognition for Hiv-1 Protease: Analysis of Crystal Structures of Six Substrate Complexes
- 3oxc: Wild Type Hiv-1 Protease with Antiviral Drug Saquinavir
- 1kzk: Je-2147-hiv Protease Complex
- 3ok9: Crystal Structure of Wild-type Hiv-1 Protease with New Oxatricyclic Designed Inhibitor Grl-0519a
- 3nuo: Crystal Structure of Hiv-1 Protease Mutant L90M with Antiviral Drug Amprenavir
- 3nuj: Crystal Structure of Hiv-1 Protease Mutant I54V with Antiviral Drug Amprenavir
- 3nu9: Crystal Structure of Hiv-1 Protease Mutant I84V with Antiviral Drug Amprenavir
- 3nu6: Crystal Structure of Hiv-1 Protease Mutant I54M with Antiviral Drug Amprenavir
- 3nu5: Crystal Structure of Hiv-1 Protease Mutant I50V with Antiviral Drug Amprenavir
- 3nu4: Crystal Structure of Hiv-1 Protease Mutant V32I with Antiviral Drug Amprenavir
- 3nu3: Wild Type Hiv-1 Protease with Antiviral Drug Amprenavir
- 1lv1: Crystal Structure Analysis of The Non-active Site Mutant of Tethered Hiv-1 Protease to 2.1a Resolution
- 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
- 1m0b: Hiv-1 Protease in Complex with an Ethyleneamine Inhibitor
- 3n3i: Crystal Structure of G48V/C95F Tethered Hiv-1 Protease/saquinavir Complex
- 1mer: Hiv-1 Mutant (I84V) Protease Complexed with Dmp450
- 1mes: Hiv-1 Mutant (I84V) Protease Complexed with Dmp323
- 1met: Hiv-1 Mutant (V82F) Protease Complexed with Dmp323
- 1meu: Hiv-1 Mutant (V82F, I84V) Protease Complexed with Dmp323
- 3mxe: Crystal Structure of Hiv-1 Protease Inhibitor, Kc32 Complexed with Wild-type Protease
- 3mxd: Crystal Structure of Hiv-1 Protease Inhibitor Kc53 in Complex with Wild-type Protease
- 1mrw: Structure of Hiv Protease (mutant Q7K L33I L63I) Complexed with Kni-577
- 1mrx: Structure of Hiv Protease (mutant Q7K L33I L63I V82F I84V ) Complexed with Kni-577
- 1msm: The Hiv Protease (mutant Q7K L33I L63I) Complexed with Kni- 764 (an Inhibitor)
- 1msn: The Hiv Protease (mutant Q7K L33I L63I V82F I84V) Complexed with Kni-764 (an Inhibitor)
- 1mt7: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
- 1mt8: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
- 1mt9: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
- 1mtb: Viability of a Drug-resistant Hiv-1 Protease Mutant: Structural Insights for Better Antiviral Therapy
- 1mtr: Hiv-1 Protease Complexed with a Cyclic Phe-ile-val Peptidomimetic Inhibitor
- 1mui: Crystal Structure of Hiv-1 Protease Complexed with Lopinavir.
- 1n49: Viability of a Drug-resistant Hiv-1 Protease Variant: Structural Insights for Better Anti-viral Therapy
- 3lzv: Structure of Nelfinavir-resistant Hiv-1 Protease (D30N/N88D) in Complex with Darunavir.
- 3lzu: Crystal Structure of a Nelfinavir Resistant Hiv-1 Crf01_ae Protease Variant (N88S) in Complex with The Protease Inhibitor Darunavir.
- 3lzs: Crystal Structure of Hiv-1 Crf01_ae Protease in Complex with Darunavir
- 1nh0: 1.03 a Structure of Hiv-1 Protease: Inhibitor Binding inside and outside The Active Site
- 1npa: Crystal Structure of Hiv-1 Protease-hup
- 1npv: Crystal Structure of Hiv-1 Protease Complexed with Ldc271
- 1npw: Crystal Structure of Hiv Protease Complexed with Lgz479
- 3kt2: Crystal Structure of N88D Mutant Hiv-1 Protease
- 1odw: Native Hiv-1 Proteinase
- 1odx: Hiv-1 Proteinase Mutant A71T, V82A
- 1ody: Hiv-1 Protease Complexed with an Inhibitor Lp-130
- 3kfs: Hiv Protease (pr) Dimer with Inhibitor Tl-3 Bound and Fragment 2f4 in The Outside/top of Flap
- 3kfr: Hiv Protease (pr) Dimer with Inhibitor Tl-3 Bound and Fragment 1f1 in The Outside/top of Flap
- 3kfp: Hiv Protease (pr) with Inhibitor Tl-3 Bound, and Dmsos in Exo Site
- 3kfn: Hiv Protease (pr) with Inhibitor Tl-3 and Fragment Hit 4d9 by Soaking
- 3kf0: Hiv Protease with Fragment 4d9 Bound
- 3kdd: Crystal Structure of Hiv-1 Protease (Q7K, L33I, L63I) in Complex with Kni-10265
- 3kdc: Crystal Structure of Hiv-1 Protease (Q7K, L33I, L63I) in Complex with Kni-10074
- 3kdb: Crystal Structure of Hiv-1 Protease (Q7K, L33I, L63I) in Complex with Kni-10006
- 3k4v: New Crystal Form of Hiv-1 Protease/saquinavir Structure Reveals Carbamylation of N-terminal Proline
- 3jw2: Hiv-1 Protease Mutant G86S with Darunavir
- 3jvy: Hiv-1 Protease Mutant G86A with Darunavir
- 3jvw: Hiv-1 Protease Mutant G86A with Symmetric Inhibitor Dmp323
- 1pro: Hiv-1 Protease Dimer Complexed with A-98881
- 3i8w: Crystal Structure of a Metallacarborane Inhibitor Bound to Hiv Protease
- 3i6o: Crystal Structure of Wild Type Hiv-1 Protease with Macrocyclic Inhibitor Grl-0216a
- 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
- 1q9p: Solution Structure of The Mature Hiv-1 Protease Monomer
- 1qbr: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
- 1qbs: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
- 1qbt: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
- 1qbu: Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
- 3hdk: Crystal Structure of Chemically Synthesized [aib51/51']hiv-1 Protease
- 3hbo: Crystal Structure of Chemically Synthesized [d-ala51/51']hiv-1 Protease
- 3h5b: Crystal Structure of Wild Type Hiv-1 Protease with Novel P1'-ligand Grl-02031
- 1rl8: Crystal Structure of The Complex of Resistant Strain of Hiv- 1 PROTEASE(V82A Mutant) with Ritonavir
- 1rpi: Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity
- 1rq9: Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity
- 3ggu: Hiv Pr Drug Resistant Patient's Variant in Complex with Darunavir
- 1rv7: Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity
- 3fx5: Structure of Hiv-1 Protease in Complex with Potent Inhibitor Kni-272 Determined by High Resolution X-ray Crystallography
- 3fsm: Crystal Structure of a Chemically Synthesized 203 Amino Acid 'covalent Dimer' [l-ala51,d-ala51'] Hiv-1 Protease Molecule
- 1sdt: Crystal Structures of Hiv Protease V82A and L90M Mutants Reveal Changes in Indinavir Binding Site.
- 1sdu: Crystal Structures of Hiv Protease V82A and L90M Mutants Reveal Changes in Indinavir Binding Site.
- 1sdv: Crystal Structures of Hiv Protease V82A and L90M Mutants Reveal Changes in Indinavir Binding Site.
- 1sgu: Comparing The Accumulation of Active Site and Non-active Site Mutations in The Hiv-1 Protease
- 1sh9: Comparing The Accumulation of Active Site and Non-active Site Mutations in The Hiv-1 Protease
- 3fiv: Crystal Structure of Feline Immunodeficiency Virus Protease Complexed with a Substrate
- 1sp5: Crystal Structure of Hiv-1 Protease Complexed with a Product of Autoproteolysis
- 1t3r: Hiv Protease Wild-type in Complex with Tmc114 Inhibitor
- 1t7i: The Structural and Thermodynamic Basis for The Binding of Tmc114, a Next-generation Hiv-1 Protease Inhibitor.
- 1t7j: Crystal Structure of Inhibitor Amprenavir in Complex with a Multi-drug Resistant Variant of Hiv-1 Protease (L63P/V82T/I84V)
- 1t7k: Crystal Structure of Hiv Protease Complexed with Arylsulfonamide Azacyclic Urea
- 3em6: Crystal Structure of I50L/A71V Mutant of Hiv-1 Protease in Complex with Inhibitor Darunavir
- 3em4: Crystal Structure of Atazanavir (atv) in Complex with I50L/A71V Drug-resistant Hiv-1 Protease
- 3em3: Crystal Structure of Amprenavir (apv) in Complex with a Drug Resistant Hiv-1 Protease Variant (I50L/A71V).
- 1tcw: Siv Protease Complexed with Inhibitor Sb203386
- 1tcx: Hiv Triple Mutant Protease Complexed with Inhibitor Sb203386
- 3el9: Crystal Structure of Atazanavir (atv) in Complex with a Multidrug Hiv-1 Protease (V82T/I84V)
- 3el4: Crystal Structure of Inhibitor Saquinavir (sqv) Complexed with The Multidrug Hiv-1 Protease Variant L63P/V82T/I84V
- 3el1: Crystal Structure of Wild-type Hiv Protease in Complex with The Inhibitor, Atazanavir
- 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)
- 3eky: Crystal Structure of Wild-type Hiv Protease in Complex with The Inhibitor, Atazanavir
- 3ekx: Crystal Structure of The Wild-type Hiv-1 Protease with The Inhibitor, Nelfinavir
- 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.
- 3ekv: Crystal Structure of The Wild Type Hiv-1 Protease with The Inhibitor, Amprenavir
- 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.)
- 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)
- 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
- 1tsq: Crystal Structure of AP2V Substrate Variant of Nc-p1 Decamer Peptide in Complex with V82A/D25N Hiv-1 Protease Mutant
- 1tsu: Crystal Structure of Decamer Ncp1 Substrate Peptide in Complex with Wild-type D25N Hiv-1 Protease Variant
- 1tw7: Wide Open 1.3a Structure of a Multi-drug Resistant Hiv-1 Protease Represents a Novel Drug Target
- 3dox: X-ray Structure of Hiv-1 Protease in Situ Product Complex
- 1u8g: Crystal Structure of a Hiv-1 Protease in Complex with Peptidomimetic Inhibitor Ki2-phe-glu-glu-nh2
- 3dk1: Wild Type Hiv-1 Protease with Potent Antiviral Inhibitor Grl-0105a
- 3djk: Wild Type Hiv-1 Protease with Potent Antiviral Inhibitor Grl-0255a
- 3dcr: X-ray Structure of Hiv-1 Protease and Hydrated Form of Ketomethylene Isostere Inhibitor
- 3dck: X-ray Structure of D25N Chemical Analogue of Hiv-1 Protease Complexed with Ketomethylene Isostere Inhibitor
- 3d3t: Crystal Structure of Hiv-1 Crf01_ae in Complex with The Substrate P1-p6
- 3d20: Crystal Structure of Hiv-1 Mutant I54V and Inhibitor Darunavia
- 3d1z: Crystal Structure of Hiv-1 Mutant I54M and Inhibitor Darunavir
- 3d1y: Crystal Structure of Hiv-1 Mutant I54V and Inhibitor Saquina
- 3d1x: Crystal Structure of Hiv-1 Mutant I54M and Inhibitor Saquinavir
- 3cyx: Crystal Structure of Hiv-1 Mutant I50V and Inhibitor Saquinavira
- 3cyw: Effect of Flap Mutations on Structure of Hiv-1 Protease and Inhibition by Saquinavir and Darunavir
- 3ckt: Hiv-1 Protease in Complex with a Dimethylallyl Decorated Pyrrolidine Based Inhibitor (orthorombic Space Group)
- 1vij: Hiv-1 Protease Complexed with The Inhibitor Hoe/bay 793 Hexagonal Form
- 1vik: Hiv-1 Protease Complexed with The Inhibitor Hoe/bay 793 Orthorhombic Form
- 3bxs: Crystal Structures of Highly Constrained Substrate and Hydrolysis Products Bound to Hiv-1 Protease. Implications for Catalytic Mechanism
- 3bxr: Crystal Structures of Highly Constrained Substrate and Hydrolysis Products Bound to Hiv-1 Protease. Implications for Catalytic Mechanism
- 3bvb: Cystal Structure of Hiv-1 Active Site Mutant D25N and Inhibitor Darunavir
- 3bva: Cystal Structure of Hiv-1 Active Site Mutant D25N and P2-nc Analog Inhibitor
- 3bhe: Hiv-1 Protease in Complex with a Three Armed Pyrrolidine Derivative
- 3bgc: Hiv-1 Protease in Complex with a Benzyl Decorated Oligoamine
- 3bgb: Hiv-1 Protease in Complex with a Isobutyl Decorated Oligoamine
- 1w5v: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
- 1w5w: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
- 1w5x: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
- 1w5y: Hiv-1 Protease in Complex with Fluoro Substituted Diol- Based C2-symmetric Inhibitor
- 3bc4: I84V Hiv-1 Protease in Complex with a Pyrrolidine Diester
- 3b80: Hiv-1 Protease Mutant I54V Complexed with Gem-diol-amine Intermediate Nlltqi
- 3b7v: Hiv-1 Protease Complexed with Gem-diol-amine Tetrahedral Intermediate Nlltqi
- 3aid: A New Class of Hiv-1 Protease Inhibitor: The Crystallographic Structure, Inhibition and Chemical Synthesis of an Aminimide Peptide Isostere
- 3a2o: Crystal Structure of Hiv-1 Protease Complexed with Kni-1689
- 2zye: Structure of Hiv-1 Protease in Complex with Potent Inhibitor Kni-272 Determined by Neutron Crystallography
- 2zga: Hiv-1 Protease in Complex with a Dimethylallyl Decorated Pyrrolidine Based Inhibitor (hexagonal Space Group)
- 2z54: The Influence of I47A Mutation on Reduced Susceptibility to The Protease Inhibitor Lopinavir
- 2z4o: Wild Type Hiv-1 Protease with Potent Antiviral Inhibitor Grl-98065
- 1xl2: Hiv-1 Protease in Complex with Pyrrolidinmethanamine
- 1xl5: Hiv-1 Protease in Complex with Amidhyroxysulfone
- 2wl0: Hiv-1 Protease Inhibitors Containing a Tertiary Alcohol in The Transition-state Mimic with Improved Cell-based Antiviral Activity
- 2wkz: Hiv-1 Protease Inhibitors Containing a Tertiary Alcohol in The Transition-state Mimic with Improved Cell-based Antiviral Activity
- 1ytg: Siv Protease Crystallized with Peptide Product
- 1yth: Siv Protease Crystallized with Peptide Product
- 1yti: Siv Protease Crystallized with Peptide Product
- 1ytj: Siv Protease Crystallized with Peptide Product
- 2whh: Hiv-1 Protease Tethered Dimer Q-product Complex along with Nucleophilic Water Molecule
- 1z1h: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 3
- 1z1r: Hiv-1 Protease Complexed with Macrocyclic Peptidomimetic Inhibitor 2
- 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
- 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
- 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
- 1zlf: Crystal Structure of a Complex of Mutant Hiv-1 Protease (A71V, V82T, I84V) with a Hydroxyethylamine Peptidomimetic Inhibitor
- 1zp8: Hiv Protease with Inhibitor Ab-2
- 1zpa: Hiv Protease with Scripps Ab-3 Inhibitor
- 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
- 1zsf: Crystal Structure of Complex of a Hydroxyethylamine Inhibitor with Hiv-1 Protease at 2.0a Resolution
- 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
- 1ztz: Crystal Structure of Hiv Protease- Metallacarborane Complex
- 2a1e: High Resolution Structure of Hiv-1 Pr with Ts-126
- 2a4f: Synthesis and Activity of N-axyl Azacyclic Urea Hiv-1 Protease Inhibitors with High Potency against Multiple Drug Resistant Viral Strains.
- 2aid: Structure of a Non-peptide Inhibitor Complexed with Hiv-1 Protease: Developing a Cycle of Structure-based Drug Design
- 2aoc: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Substrate Analog P2-nc
- 2aod: Crystal Structure Analysis of Hiv-1 Protease with a Substrate Analog P2-nc
- 2aoe: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog Ca-p2
- 2aof: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog P1-p6
- 2aog: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog P2-nc
- 2aoh: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Substrate Analog P6-pr
- 2aoi: Crystal Structure Analysis of Hiv-1 Protease with a Substrate Analog P1-p6
- 2aoj: Crystal Structure Analysis of Hiv-1 Protease with a Substrate Analog P6-pr
- 2uy0: Two-carbon-elongated Hiv-1 Protease Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic
- 2uxz: Two-carbon-elongated Hiv-1 Protease Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic
- 2aqu: Structure of Hiv-1 Protease Bound to Atazanavir
- 2avm: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
- 2avo: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
- 2avq: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
- 2avs: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
- 2avv: Kinetics, Stability, and Structural Changes in High Resolution Crystal Structures of Hiv-1 Protease with Drug Resistant Mutations L24I, I50V, and G73S
- 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)
- 2az8: Hiv-1 Protease Nl4-3 in Complex with Inhibitor, Tl-3
- 2az9: Hiv-1 Protease Nl4-3 1x Mutant
- 2azb: Hiv-1 Protease Nl4-3 3x Mutant in Complex with Inhibitor, Tl-3
- 2azc: Hiv-1 Protease Nl4-3 6x Mutant
- 2bb9: Structure of Hiv1 Protease and AKC4P_133A Complex.
- 2bbb: Structure of Hiv1 Protease and Hh1_173_3a Complex.
- 2rkg: Hiv-1 Pr Resistant Mutant + Lpv
- 2rkf: Hiv-1 Pr Resistant Mutant + Lpv
- 2bpv: Hiv-1 Protease-inhibitor Complex
- 2bpw: Hiv-1 Protease-inhibitor Complex
- 2bpx: Hiv-1 Protease-inhibitor Complex
- 2bpy: Hiv-1 Protease-inhibitor Complex
- 2bpz: Hiv-1 Protease-inhibitor Complex
- 2bqv: Hiv-1 Protease in Complex with Inhibitor Aha455
- 2r43: I50V Hiv-1 Protease in Complex with an Amino Decorated Pyrrolidine-based Inhibitor
- 2r3w: I84V Hiv-1 Protease in Complex with a Amino Decorated Pyrrolidine-based Inhibitor
- 2r3t: I50V Hiv-1 Protease Mutant in Complex with a Carbamoyl Decorated Pyrrolidine-based Inhibitor
- 2r38: I84V Hiv-1 Protease Mutant in Complex with a Carbamoyl Decorated Pyrrolidine-based Inhibitor
- 2qnq: Hiv-1 Protease in Complex with a Chloro Decorated Pyrrolidine-based Inhibitor
- 2qnp: Hiv-1 Protease in Complex with a Iodo Decorated Pyrrolidine- Based Inhibitor
- 2qnn: Hiv-1 Protease in Complex with a Multiple Decorated Pyrrolidine-based Inhibitor
- 2qmp: Crystal Structure of Hiv-1 Protease Complexed with Pl-100
- 2cej: P1' Extended Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol in The Transition-state Mimicking Scaffold
- 2cem: P1' Extended Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol in The Transition-state Mimicking Scaffold
- 2cen: P1' Extended Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol in The Transition-state Mimicking Scaffold
- 2qhc: The Influence of I47A Mutation on Reduced Susceptibility to The Protease Inhibitor Lopinavir
- 2qd8: Hiv-1 Protease Mutant I84V with Potent Antiviral Inhibitor Grl-98065
- 2qd7: Hiv-1 Protease Mutant V82A with Potent Antiviral Inhibitor Grl-98065
- 2qd6: Hiv-1 Protease Mutant I50V with Potent Antiviral Inhibitor Grl-98065
- 2qci: Hiv-1 Protease Mutant D30N with Potent Antiviral Inhibitor Grl-98065
- 2qak: Hiv-1 Pr Mutant in Complex with Nelfinavir
- 2q64: Hiv-1 Pr Mutant in Complex with Nelfinavir
- 2q63: Hiv-1 Pr Mutant in Complex with Nelfinavir
- 2pyn: Hiv-1 Pr Mutant in Complex with Nelfinavir
- 2pym: Hiv-1 Pr Mutant in Complex with Nelfinavir
- 2pwr: Hiv-1 Protease in Complex with a Carbamoyl Decorated Pyrrolidine-based Inhibitor
- 2pwc: Hiv-1 Protease in Complex with a Amino Decorated Pyrrolidine-based Inhibitor
- 2pqz: Hiv-1 Protease in Complex with a Pyrrolidine-based Inhibitor
- 2pc0: Apo Wild-type Hiv Protease in The Open Conformation
- 2p3d: Crystal Structure of The Multi-drug Resistant Mutant Subtype F Hiv Protease Complexed with Tl-3 Inhibitor
- 2p3c: Crystal Structure of The Subtype F Wild Type Hiv Protease Complexed with Tl-3 Inhibitor
- 2p3b: Crystal Structure of The Subtype B Wild Type Hiv Protease Complexed with Tl-3 Inhibitor
- 2p3a: Crystal Structure of The Multi-drug Resistant Mutant Subtype B Hiv Protease Complexed with Tl-3 Inhibitor
- 6y9z: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,9)
- 6y9y: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-7,13)
- 6y9x: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,7)
- 6y9w: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-13,8)
- 6y9v: Structure of The Native Full-length Hiv-1 Capsid Protein in Complex with Cyclophilin a from Helical Assembly (-8,13)
- 2o40: Crystal Structure of a Chemically Synthesized 203 Amino Acid 'covalent Dimer' Hiv-1 Protease Molecule
- 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
- 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
- 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
- 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
- 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
- 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
- 2nxm: Structure of Hiv-1 Protease D25N Complexed with The Rt-rh Analogue Peptide Gly-ala-gln-thr-phe*tyr-val-asp-gly-ala
- 2nxl: Structure of Hiv-1 Protease D25N Complexed with The Rt-rh Analogue Peptide Gly-ala-glu-val-phe*tyr-val-asp-gly-ala
- 2nxd: Structure of Hiv-1 Protease D25N Complexed with Rt-rh Analogue Peptide Gly-ala-asp-ile-phe*tyr-leu-asp-gly-ala
- 2nph: Crystal Structure of Hiv1 Protease in Situ Product Complex
- 2nnp: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Inhibitor Saquinavir
- 2nnk: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Inhibitor Saquinavir
- 2nmz: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Inhibitor Saquinavir
- 2nmy: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Inhibitor Saquinavir
- 2f3k: Substrate Envelope and Drug Resistance: Crystal Structure of R01 in Complex with Wild-type Hiv-1 Protease
- 2f80: Hiv-1 Protease Mutant D30N Complexed with Inhibitor Tmc114
- 2f81: Hiv-1 Protease Mutant L90M Complexed with Inhibitor Tmc114
- 2f8g: Hiv-1 Protease Mutant I50V Complexed with Inhibitor Tmc114
- 2fdd: Crystal Structure of Hiv Protease D545701 Bound with Gw0385
- 2fde: Wild Type Hiv Protease Bound with Gw0385
- 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.
- 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.
- 2fiv: Crystal Structure of Feline Immunodeficiency Virus Protease Complexed with a Substrate
- 2fns: Crystal Structure of Wild-type Inactive (D25N) Hiv-1 Protease Complexed with Wild-type Hiv-1 Nc-p1 Substrate.
- 2fnt: Crystal Structure of a Drug-resistant (V82A) Inactive (D25N) Hiv-1 Protease Complexed with AP2V Variant of Hiv-1 Nc-p1 Substrate.
- 2fxd: X-ray Crystal Structure of Hiv-1 Protease Irm Mutant Complexed with Atazanavir (bms-232632)
- 2fxe: X-ray Crystal Structure of Hiv-1 Protease Crm Mutant Complexed with Atazanavir (bms-232632)
- 2g69: Structure of Unliganded Hiv-1 Protease F53L Mutant
- 5yrs: X-ray Snapshot of Hiv-1 Protease in Action: Observation of Tetrahedral Intermediate and Its Sihb with Catalytic Aspartate
- 5yoj: Structure of A17 Hiv-1 Protease in Complex with Inhibitor Kni-1657
- 2hah: The Structure of Fiv 12s Protease in Complex with Tl-3
- 2hb2: Structure of Hiv Protease 6x Mutant in Apo Form
- 2hb4: Structure of Hiv Protease Nl4-3 in an Unliganded State
- 2hc0: Structure of Hiv Protease 6x Mutant in Complex with Ab-2.
- 2hs1: Ultra-high Resolution X-ray Crystal Structure of Hiv-1 Protease V32I Mutant with Tmc114 (darunavir) Inhibitor
- 2hs2: Crystal Structure of M46L Mutant of Hiv-1 Protease Complexed with Tmc114 (darunavir)
- 2i4d: Crystal Structure of Wt Hiv-1 Protease with Gs-8373
- 2i4u: Hiv-1 Protease with Tmc-126
- 2i4v: Hiv-1 Protease I84V, L90M with Tmc126
- 2i4w: Hiv-1 Protease Wt with Gs-8374
- 2i4x: Hiv-1 Protease I84V, L90M with Gs-8374
- 2idw: Crystal Structure Analysis of Hiv-1 Protease Mutant V82A with a Potent Non-peptide Inhibitor (uic-94017)
- 2ien: Crystal Structure Analysis of Hiv-1 Protease with a Potent Non-peptide Inhibitor (uic-94017)
- 2ieo: Crystal Structure Analysis of Hiv-1 Protease Mutant I84V with a Potent Non-peptide Inhibitor (uic-94017)
- 2jo0: The Solution Structure of The Monomeric Species of The C Terminal Domain of The Ca Protein of Hiv-1
- 3oy4: Crystal Structure of Hiv-1 L76V Protease in Complex with The Protease Inhibitor Darunavir.
- 3hau: Crystal Structure of Chemically Synthesized Hiv-1 Protease with Reduced Isostere Mvt-101 Inhibitor
- 3haw: Crystal Structure of [l-ala51/51']hiv-1 Protease with Reduced Isostere Mvt-101 Inhibitor
- 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
- 3i2l: Crystal Structure of a Chemically Synthesized [allo-ile50/50']hiv-1 Protease Molecule Complexed with Mvt-101 Reduced Isostere Inhibitor
- 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
- 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
- 3mws: Crystal Structure of Group N Hiv-1 Protease
- 3pwm: Hiv-1 Protease Mutant L76V with Darunavir
- 3pwr: Hiv-1 Protease Mutant L76V Complexed with Saquinavir
- 3qin: Crystal Structure of Hiv-1 Rnase H P15 with Engineered E. Coli Loop and Pyrimidinol Carboxylic Acid Inhibitor
- 3qio: Crystal Structure of Hiv-1 Rnase H with Engineered E. Coli Loop and N- Hydroxy Quinazolinedione Inhibitor
- 3qip: Structure of Hiv-1 Reverse Transcriptase in Complex with an Rnase H Inhibitor and Nevirapine
- 6p9b: Hiv-1 Protease Multiple Drug Resistant Mutant PRS5B with Amprenavir
- 6p9a: Hiv-1 Protease Multiple Mutant PRS5B with Darunavir
- 3hlo: Crystal Structure of Chemically Synthesized 'covalent Dimer' [gly51/d- Ala51']hiv-1 Protease
- 3ia9: Crystal Structure of a Chemically Synthesized [D25N]HIV-1 Protease Molecule Complexed with Mvt-101 Reduced Isostere Inhibitor
- 3ndt: Hiv-1 Protease Saquinavir:ritonavir 1:1 Complex Structure
- 3ndu: Hiv-1 Protease Saquinavir:ritonavir 1:5 Complex Structure
- 3ndw: Hiv-1 Protease Saquinavir:ritonavir 1:15 Complex Structure
- 3ndx: Hiv-1 Protease Saquinavir:ritonavir 1:50 Complex Structure
- 6ujx: Hiv-1 Wild-type Reverse Transcriptase-dna Complex with (-)-ftc-tp
- 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
- 3st5: Crystal Structure of Wild-type Hiv-1 Protease with C3-substituted Hexahydrocyclopentafuranyl Urethane as P2-ligand, Grl-0489a
- 3nls: Crystal Structure of Hiv-1 Protease in Complex with Kni-10772
- 3oxv: Crystal Structure of Hiv-1 I50V, A71 Protease in Complex with The Protease Inhibitor Amprenavir.
- 3oxw: Crystal Structure of Hiv-1 I50V, A71V Protease in Complex with The Protease Inhibitor Darunavir
- 3oxx: Crystal Structure of Hiv-1 I50V, A71V Protease in Complex with The Protease Inhibitor Atazanavir
- 3th9: Crystal Structure of Hiv-1 Protease Mutant Q7K V32I L63I with a Cyclic Sulfonamide Inhibitor
- 3so9: Darunavir in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
- 3spk: Tipranavir in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
- 3tam: Crystal Structure of Hiv-1 Reverse Transcriptase (K103N Mutant) in Complex with Inhibitor M06
- 3nwq: X-ray Structure of Ester Chemical Analogue [o-ile50,o-ile50']hiv-1 Protease Complexed with Mvt-101
- 3nwx: X-ray Structure of Ester Chemical Analogue [o-ile50,o-ile50']hiv-1 Protease Complexed with Kvs-1 Inhibitor
- 3nxe: X-ray Structure of Ester Chemical Analogue 'covalent Dimer' [ile50,o- Ile50']hiv-1 Protease Complexed with Mvt-101 Inhibitor
- 3nxn: X-ray Structure of Ester Chemical Analogue 'covalent Dimer' [ile50,o- Ile50']hiv-1 Protease Complexed with Kvs-1 Inhibitor
- 3nyg: X-ray Structure of Ester Chemical Analogue [o-gly51,o-gly51']hiv-1 Protease Complexed with Mvt-101 Inhibitor
- 2xye: Hiv-1 Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic and Various P2 and P1 Prime Substituents
- 2xyf: Hiv-1 Inhibitors with a Tertiary-alcohol-containing Transition-state Mimic and Various P2 and P1 Prime Substituents
- 3psu: Hiv-1 Protease in Complex with an Isobutyl Decorated Oligoamine (symmetric Binding Mode)
- 3qaa: Hiv-1 Wild Type Protease with a Substituted Bis-tetrahydrofuran Inhibitor, Grl-044-10a
- 3qbf: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
- 3u7s: Hiv Pr Drug Resistant Patient's Variant in Complex with Darunavir
- 3qih: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Novel Inhibitor
- 6prf: Hiv-1 Protease Multiple Drug Resistant Clinical Isolate Mutant Pr20 with Grl-14213a
- 3qn8: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Novel Inhibitor
- 3qp0: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Novel Inhibitor
- 3qpj: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
- 3qrm: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
- 3qro: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
- 3qrs: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Three-armed Pyrrolidine-based Inhibitor
- 3s43: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Amprenavir
- 3s53: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Darunavir in Space Group P212121
- 3s54: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Darunavir in Space Group P21212
- 3s56: Hiv-1 Protease Triple Mutants V32I, I47V, V82I with Antiviral Drug Saquinavir
- 6o9e: Structure of Hiv-1 Reverse Transcriptase in Complex with Dna and Indopy-1
- 4dfg: Crystal Structure of Wild-type Hiv-1 Protease with Cyclopentyltetrahydro- Furanyl Urethanes as P2-ligand, Grl-0249a
- 3uhl: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 in Complex with P2-nc Substrate Analog
- 3tkg: Crystal Structure of Hiv Model Protease Precursor/saquinavir Complex
- 3tkw: Crystal Structure of Hiv Protease Model Precursor/darunavir Complex
- 3tl9: Crystal Structure of Hiv Protease Model Precursor/saquinavir Complex
- 4a6b: Stereoselective Synthesis, X-ray Analysis, and Biological Evaluation of a New Class of Lactam Based Hiv-1 Protease Inhibitors
- 4a6c: Stereoselective Synthesis, X-ray Analysis, and Biological Evaluation of a New Class of Lactam Based Hiv-1 Protease Inhibitors
- 4ep2: Crystal Structure of Inactive Single Chain Wild-type Hiv-1 Protease in Complex with The Substrate Rt-rh
- 4ep3: Crystal Structure of Inactive Single Chain Wild-type Hiv-1 Protease in Complex with The Substrate Ca-p2
- 4epj: Crystal Structure of Inactive Single Chain Wild-type Hiv-1 Protease in Complex with The Substrate P2-nc
- 4eq0: Crystal Structure of Inactive Single Chain Variant of Hiv-1 Protease in Complex with The Substrate P2-nc
- 4eqj: Crystal Structure of Inactive Single Chain Variant of Hiv-1 Protease in Complex with The Substrate Rt-rh
- 3t3c: Structure of Hiv Pr Resistant Patient Derived Mutant (comprising 22 Mutations) in Complex with Drv
- 4fe6: Crystal Structure of Hiv-1 Protease in Complex with an Enamino- Oxindole Inhibitor
- 3tof: Hiv-1 Protease - Epoxydic Inhibitor Complex (ph 6 - Orthorombic Crystal Form P212121)
- 3tog: Hiv-1 Protease - Epoxydic Inhibitor Complex (ph 9 - Monoclinic Crystal Form P21)
- 3toh: Hiv-1 Protease - Epoxydic Inhibitor Complex (ph 9 - Orthorombic Crystal Form P212121)
- 3t11: Dimeric Inhibitor of Hiv-1 Protease.
- 3ttp: Structure of Multiresistant Hiv-1 Protease in Complex with Darunavir
- 4fae: Substrate P2/nc in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
- 4faf: Substrate Ca/p2 in Complex with a Human Immunodeficiency Virus Type 1 Protease Variant
- 6ixd: X-ray Crystal Structure of Bpi-11 Hiv-1 Protease Complex
- 4fl8: Hiv-1 Protease Complexed with Gem-diol-amine Tetrahedral Intermediate
- 4flg: Hiv-1 Protease Mutant I47V Complexed with Reaction Intermediate
- 4fm6: Hiv-1 Protease Mutant V32I Complexed with Reaction Intermediate
- 3vf5: Crystal Structure of Hiv-1 Protease Mutant I47V with Novel P1'-ligands Grl-02031
- 3vf7: Crystal Structure of Hiv-1 Protease Mutant L76V with Novel P1'-ligands Grl-02031
- 3vfa: Crystal Structure of Hiv-1 Protease Mutant V82A with Novel P1'-ligands Grl-02031
- 3vfb: Crystal Structure of Hiv-1 Protease Mutant N88D with Novel P1'-ligands Grl-02031
- 4a4q: Stereoselective Synthesis, X-ray Analysis, and Biological Evaluation of a New Class of Lactam Based Hiv-1 Protease Inhibitors
- 2fmb: Eiav Protease Complexed with an Inhibitor Lp-130
- 4b3o: Structures of Hiv-1 Rt and Rna-dna Complex Reveal a Unique Rt Conformation and Substrate Interface
- 4b3p: Structures of Hiv-1 Rt and Rna-dna Complex Reveal a Unique Rt Conformation and Substrate Interface
- 4b3q: Structures of Hiv-1 Rt and Rna-dna Complex Reveal a Unique Rt Conformation and Substrate Interface
- 4i2p: Crystal Structure of Hiv-1 Reverse Transcriptase in Complex with Rilpivirine (tmc278) Based Analogue
- 4i2q: Crystal Structure of K103N/Y181C Mutant of Hiv-1 Reverse Transcriptase in Complex with Rilpivirine (tmc278) Analogue
- 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
- 4ej8: Apo Hiv Protease (pr) Dimer in Closed Form with Fragment 1f1 in The Outside/top of Flap
- 4ejd: Hiv Protease (pr) Dimer in Closed Form with Pepstatin in Active Site and Fragment 1f1 in The Outside/top of Flap
- 4ejk: Hiv Protease (pr) Dimer in Closed Form with Pepstatin in Active Site and Fragment 1f1-n in The Outside/top of Flap
- 4ejl: Apo Hiv Protease (pr) Dimer in Closed Form with Fragment 1f1-n in The Outside/top of Flap
- 4gvm: Hiv-1 Integrase Catalytic Core Domain A128T Mutant Complexed with Allosteric Inhibitor
- 4gw6: Hiv-1 Integrase Catalytic Core Domain Complexed with Allosteric Inhibitor
- 4id1: Hiv-1 Integrase Catalytic Core Domain Complexed with Allosteric Inhibitor
- 4f73: Crystal Structure of Active Hiv-1 Protease in Complex with The N Terminal Product of Ca-p2 Cleavage Site
- 4f74: Crystal Structure of Active Hiv-1 Protease in Complex with The N Terminal Product of The Substrate Ma-ca.
- 4f75: Crystal Structure of Active Hiv-1 Protease in Complex with The N Terminal Product of The Substrate Rh-in
- 4f76: Crystal Structure of The Active Hiv-1 Protease in Complex with The Products of P1-p6 Substrate
- 4j54: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 with The Potent Antiviral Inhibitor Grl-0519a
- 4j55: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 with The Potent Antiviral Inhibitor Grl-02031
- 4j5j: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 in Complex with Amprenavir
- 4hla: Crystal Structure of Wild Type Hiv-1 Protease in Complex with Darunavir
- 4i8w: Crystal Structure of Wild Type Hiv-1 Protease in Complex with Non- Peptidic Inhibitor, Grl007
- 4i8z: Crystal Structure of Wild Type Hiv-1 Protease in Complex with Non- Peptidic Inhibitor, Grl008
- 4jec: Joint Neutron and X-ray Structure of Per-deuterated Hiv-1 Protease in Complex with Clinical Inhibitor Amprenavir
- 4gb2: Hiv-1 Protease (mutant Q7K L33I L63I) in Complex with a Bicyclic Pyrrolidine Inhibitor
- 3zps: Design and Synthesis of P1-p3 Macrocyclic Tertiary Alcohol Comprising Hiv-1 Protease Inhibitors
- 3zpt: Design and Synthesis of P1-p3 Macrocyclic Tertiary Alcohol Comprising Hiv-1 Protease Inhibitors
- 3zpu: Design and Synthesis of P1-p3 Macrocyclic Tertiary Alcohol Comprising Hiv-1 Protease Inhibitors
- 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
- 4gye: Mdr 769 Hiv-1 Protease in Complex with Reduced P1F
- 4gzf: Multi-drug Resistant Hiv-1 Protease 769 Variant with Reduced Lrf Peptide
- 4hdb: Crystal Structure of Hiv-1 Protease Mutants D30N Complexed with Inhibitor Grl-0519
- 4hdf: Crystal Structure of Hiv-1 Protease Mutants V82A Complexed with Inhibitor Grl-0519
- 4hdp: Crystal Structure of Hiv-1 Protease Mutants I50V Complexed with Inhibitor Grl-0519
- 4he9: Crystal Structure of Hiv-1 Protease Mutants I54M Complexed with Inhibitor Grl-0519
- 4heg: Crystal Structure of Hiv-1 Protease Mutants R8Q Complexed with Inhibitor Grl-0519
- 4jmu: Crystal Structure of Hiv Matrix Residues 1-111 in Complex with Inhibitor
- 4k4p: Tl-3 Inhibited TRP6ALA Hiv Protease
- 4k4q: Tl-3 Inhibited TRP6ALA Hiv Protease with 3-bromo-2,6-dimethoxybenzoic Acid Bound in Flap Site
- 4k4r: Tl-3 Inhibited TRP6ALA Hiv Protease with 1-bromo-2-napthoic Acid Bound in Exosite
- 4kb9: Crystal Structure of Wild-type Hiv-1 Protease with Novel Tricyclic P2- Ligands Grl-0739a
- 4m8x: Gs-8374, a Novel Phosphonate-containing Inhibitor of Hiv-1 Protease, Effectively Inhibits Hiv Pr Mutants with Amino Acid Insertions
- 4m8y: Gs-8374, a Novel Phosphonate-containing Inhibitor of Hiv-1 Protease, Effectively Inhibits Hiv Pr Mutants with Amino Acid Insertions
- 4mc1: Hiv Protease in Complex with SA526P
- 4mc2: Hiv Protease in Complex with SA525P
- 4mc6: Hiv Protease in Complex with Sa499
- 4mc9: Hiv Protease in Complex with Aa74
- 4qgi: X-ray Crystal Structure of Hiv-1 Protease Variant G48T/L89M in Complex with Saquinavir
- 4qj2: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with Wt P1-p6 Substrate
- 4qj6: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with P1-p6 Substrate Variant (L449F)
- 4qj7: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with P1-p6 Substrate Variant (R452S)
- 4qj8: Crystal Structure of Inactive Hiv-1 Protease Variant (I50V/A71V) in Complex with P1-p6 Substrate Variant (P453L)
- 4qj9: Crystal Structure of Inactive Hiv-1 Protease in Complex with P1-p6 Substrate Variant (R452S)
- 4qja: Crystal Structure of Inactive Hiv-1 Protease in Complex with P1-p6 Substrate Variant (P453L)
- 4qlh: Crystal Structure of Drug Resistant V82S/V1082S Hiv-1 Protease
- 5vj3: Hiv Protease (pr) in Open Form with Mg2+ in Active Site and Hive-9 in Eye Site
- 4u8w: Hiv-1 Wild Type Protease with Grl-050-10a (a Gem-difluoro-bis- Tetrahydrofuran as P2-ligand)
- 5vea: Hiv Protease (pr) with Tl-3 in Active Site and 4-methylbenzene-1,2- Diamine in Exosite
- 5vck: Hiv Protease (pr) with Tl-3 in The Active Site and (z)-n-(thiazol-2- Yl)-n'-tosylcarbamimidate in The Exosite
- 4obd: Crystal Structure of Nelfinavir-resistant, Inactive Hiv-1 Protease (D30N/N88D) in Complex with The P1-p6 Substrate Variant (L449F/S451N)
- 4obf: Crystal Structure of Nelfinavir-resistant, Inactive Hiv-1 Protease Variant (D30N/N88D) in Complex with The P1-p6 Substrate Variant (S451N)
- 4obg: Crystal Structure of Nelfinavir-resistant, Inactive Hiv-1 Protease (D30N/N88D) in Complex with The P1-p6 Substrate.
- 4obh: Crystal Structure of Inactive Hiv-1 Protease in Complex with The P1-p6 Substrate Variant (L449F)
- 4obj: Crystal Structure of Inactive Hiv-1 Protease in Complex with The P1-p6 Substrate Variant (S451N)
- 4obk: Crystal Structure of Inactive Hiv-1 Protease in Complex with The P1-p6 Substrate Variant (L449F/S451N)
- 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)
- 4coe: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cp7: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cpq: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cpr: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cps: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cpt: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cpu: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cpw: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 4cpx: Macrocyclic Transition-state Mimicking Hiv-1 Protease Inhibitors Encompassing a Tertiary Alcohol
- 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
- 5tuq: Crystal Structure of a 6-cyclohexylmethyl-3-hydroxypyrimidine-2,4- Dione Inhibitor in Complex with Hiv Reverse Transcriptase
- 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
- 5e5k: Joint X-ray/neutron Structure of Hiv-1 Protease Triple Mutant (V32I, I47V,V82I) with Darunavir at Ph 4.3
- 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
- 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
- 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
- 5bs4: Hiv-1 Wild Type Protease with Grl-047-11a (a Methylamine Bis- Tetrahydrofuran P2-ligand, 4-amino Sulfonamide Derivative)
- 5bry: Hiv-1 Wild Type Protease with Grl-011-11a (a Methylamine Bis- Tetrahydrofuran P2-ligand, Sulfonamide Isostere Derivate)
- 4q1w: Mutations outside The Active Site of Hiv-1 Protease Alter Enzyme Structure and Dynamic Ensemble of The Active Site to Confer Drug Resistance
- 4q1x: Mutations outside The Active Site of Hiv-1 Protease Alter Enzyme Structure and Dynamic Ensemble of The Active Site to Confer Drug Resistance
- 4q1y: Mutations outside The Active Site of Hiv-1 Protease Alter Enzyme Structure and Dynamic Ensemble of The Active Site to Confer Drug Resistance
- 5ah7: Disubstituted Bis-thf Moieties as New P2 Ligands in Non-peptidal Hiv-1 Protease Inhibitors (ii)
- 4zls: Hiv-1 Wild Type Protease with Grl-096-13a (a Boc-derivative P2-ligand, 3,-5-dimethylbiphenyl P1-ligand)
- 4zip: Hiv-1 Wild Type Protease with Grl-0648a (a Isophthalamide-derived P2- Ligand)
- 4q5m: D30N Tethered Hiv-1 Protease Dimer/saquinavir Complex
- 4yhq: Crystal Structure of Multidrug Resistant Clinical Isolate Pr20 with Grl-5010a
- 4ye3: Crystal Structure of Multidrug Resistant Hiv-1 Protease Clinical Isolate Pr20 with Inhibitor Grl-4410a
- 5agz: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
- 5ah6: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
- 5ah8: Disubstituted Bis-thf Moieties as New P2 Ligands in Non-peptidal Hiv-1 Protease Inhibitors (ii)
- 5ah9: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
- 5aha: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
- 5ahb: Disubstituted Bis-thf Moieties as New P2 Ligands in Non-peptidal Hiv-1 Protease Inhibitors (ii)
- 5ahc: Disubstituted Bis-thf Moieties as New P2 Ligands in Non- Peptidal Hiv-1 Protease Inhibitors (ii)
- 7ahx: Hiv-1 Reverse Transcriptase Complex with Dna and D-aspartate Tenofovir with Bound Manganese
- 7aid: Hiv-1 Reverse Transcriptase Complex with Dna and D-aspartate Tenofovir
- 7aif: Hiv-1 Reverse Transcriptase Complex with Dna and L-glutamate Tenofovir with Bound Manganese
- 7aig: Hiv-1 Reverse Transcriptase Complex with Dna and L-glutamate Tenofovir
- 7aii: Hiv-1 Reverse Transcriptase Complex with Dna and L-methionine Tenofovir with Bound Manganese
- 7aij: Hiv-1 Reverse Transcriptase Complex with Dna and L-methionine Tenofovir
- 6vug: Diabody Bound to a Reverse Transcriptase Aptamer Complex
- 7n6t: Crystal Structure of Inhibitor-free Hiv-1 Prs17 Revertant Mutant Prs17 V48G
- 7n6v: Crystal Structure of Hiv-1 Protease Multiple Mutants Prs17 with Revertant Mutation V48G Bound to Inhibitor Amprenavir
- 7n6x: Crystal Structure of Hiv-1 Protease Multiple Mutants Prs17 Bound to Inhibitor Amprenavir
- 7oxq: Crystal Structure of Hiv-1 Reverse Transcriptase with a Double Stranded Dna in Complex with Fragment 048 at The Transient P-pocket.
- 7oz2: Crystal Structure of Hiv-1 Reverse Transcriptase with a Double Stranded Dna Showing a Transient P-pocket
- 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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