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Your request to link to MMDB for Dimer of Gag-Pol polyprotein [489-587,L499I,L508Q,K509R,E524D,M525I,S526N,M535I,I539V,I543V,I551V,L552P,A560V,V571A,L579M]
| MMDB Description | |
|---|---|
| 73437 | Hiv-1 Protease in Complex With Sdz283-910 |
| 14951 | Alternate Binding Site for the P1-p3 Group of a Class of Potent Hiv-1 Protease Inhibitors as a Result of Concerted Structural Change in 80's Loop |
| 14952 | Alternate Binding Site for the P1-p3 Group of a Class of Potent Hiv-1 Protease Inhibitors as a Result of Concerted Structural Change in 80's Loop |
| 14953 | Alternate Binding Site for the P1-p3 Group of a Class of Potent Hiv-1 Protease Inhibitors as a Result of Concerted Structural Change in 80's Loop |
| 19723 | Hiv-1 Protease in Complex With the Inhibitor Bea369 |
| 73646 | Crystal Structure of a Complex of Hiv-1 Protease With a Dihydroethylene-containing Inhibitor: Comparisons With Molecular Modeling |
| 1289 | Structural Basis of Drug Resistance for the V82a Mutant of Hiv-1 Protease: Backbone Flexibility and Subsite Repacking |
| 49549 | Hiv-1 Proteinase Complexed With RO 31-8959 |
| 7007 | Hiv-1 Protease Dimer Complexed With A-84538 |
| 21361 | Inhibitor of HIV Protease With Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants |
| 21362 | Inhibitor of HIV Protease With Unusual Binding Mode Potently Inhibiting Multi-resistant Protease Mutants |
| 50612 | Native Hiv-1 Proteinase |
| 50613 | Hiv-1 Proteinase Mutant A71t, V82a |
| 4836 | Hiv-1 Protease Dimer Complexed With A-98881 |
| 30822 | Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity |
| 30824 | Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity |
| 30832 | Crystal Structures of a Multidrug-resistant Hiv-1 Protease Reveal an Expanded Active Site Cavity |
| 2155 | An Orally-bioavailable Hiv-1 Protease Inhibitor Containing an Imidazole-derived Peptide Bond Replacement. Crystallographic and Pharmacokinetic Analysis |
| 29356 | Comparing the Accumulation of Active Site and Non-active Site Mutations in the Hiv-1 Protease |
| 29357 | Comparing the Accumulation of Active Site and Non-active Site Mutations in the Hiv-1 Protease |
| 34066 | Wide Open 1.3a Structure of a Multi-drug Resistant Hiv-1 Protease Represents a Novel Drug Target |
| 9368 | Hiv-1 Protease Complexed With the Inhibitor Hoebay 793 Hexagonal Form |
| 9073 | Hiv-1 Protease Complexed With the Inhibitor Hoebay 793 Orthorhombic Form |
| 52200 | 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 |
| 52538 | Hiv-1 Protease Nl4-3 1X Mutant |
| 52539 | Hiv-1 Protease Nl4-3 3X Mutant in Complex With Inhibitor, Tl-3 |
| 42560 | Structure of Hiv-1 Protease Mutant Bound to Ritonavir |
| 42561 | Structure of Hiv-1 Protease Mutant Bound to Indinavir |
| 37729 | Crystal Structure of HIV Protease D545701 Bound With Gw0385 |
| 58047 | Three-dimensional Structure of Aspartyl Protease From Human Immunodeficiency Virus Hiv-1 |
| 45722 | Crystal Structure of the Multi-drug Resistant Mutant Subtype B HIV Protease Complexed With Tl-3 Inhibitor |
| 65553 | Crystal Structure of Hiv-1 Protease Complexed With Pl-100 |
| 66403 | I50v Hiv-1 Protease Mutant in Complex With a Carbamoyl Decorated Pyrrolidine-based Inhibitor |
| 66548 | I50v Hiv-1 Protease in Complex With an Amino Decorated Pyrrolidine- Based Inhibitor |
| 83066 | HIV Protease Complexed With Compound 10B |
| 89684 | Crystal Structures of Multidrug-resistant Clinical Isolate 769 Hiv-1 Protease Variants |
| 89685 | Crystal Structures of Multidrug-resistant Clinical Isolate 769 Hiv-1 Protease Variants |
| 89686 | Crystal Structures of Multidrug-resistant Clinical Isolate 769 Hiv-1 Protease Variants |
| 89529 | Mdr769 Hiv-1 Protease Complexed With Maca Hepta-peptide |
| 89530 | Mdr769 Hiv-1 Protease Complexed With Rtrh Hepta-peptide |
| 89531 | Mdr769 Hiv-1 Protease Complexed With Rhin Hepta-peptide |
| 89532 | Mdr769 Hiv-1 Protease Complexed With Prrt Hepta-peptide |
| 89533 | Mdr769 Hiv-1 Protease Complexed With Tfpr Hepta-peptide |
| 89534 | Mdr769 Hiv-1 Protease Complexed With P1p6 Hepta-peptide |
| 89535 | Mdr769 Hiv-1 Protease Complexed With Ncp1 Hepta-peptide |
| 89536 | Mdr769 Hiv-1 Protease Complexed With P2nc Hepta-peptide |
| 89537 | Mdr769 Hiv-1 Protease Complexed With Cap2 Hepta-peptide |
| 89695 | Crystal Structures of Multidrug-resistant Clinical Isolate 769 Hiv-1 Protease Variants |
| 3200 | X-ray Crystal Structure of the HIV Protease Complex With L- 700,417, an Inhibitor With Pseudo C2 Symmetry |
| 54778 | Crystallographic Analysis of a Complex Between Human Immunodeficiency Virus Type 1 Protease and Acetyl- Pepstatin at 2.0-angstroms Resolution |
| 54880 | Design, Activity and 2.8 Angstroms Crystal Structure of a C2 Symmetric Inhibitor Complexed to Hiv-1 Protease |