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| MMDB Description | |
|---|---|
| 73437 | Hiv-1 Protease in Complex With Sdz283-910 |
| 12513 | Counteracting Hiv-1 Protease Drug Resistance: Structural Analysis of Mutant Proteases Complexed With Xv638 and Sd146, Cyclic Urea Amides With Broad Specificities |
| 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 |
| 7495 | Hiv-1 Mutant (V82f) Protease Complexed With Dmp323 |
| 50612 | Native Hiv-1 Proteinase |
| 50613 | Hiv-1 Proteinase Mutant A71t, V82a |
| 4836 | Hiv-1 Protease Dimer Complexed With A-98881 |
| 2155 | An Orally-bioavailable Hiv-1 Protease Inhibitor Containing an Imidazole-derived Peptide Bond Replacement. Crystallographic and Pharmacokinetic Analysis |
| 9368 | Hiv-1 Protease Complexed With the Inhibitor Hoebay 793 Hexagonal Form |
| 9073 | Hiv-1 Protease Complexed With the Inhibitor Hoebay 793 Orthorhombic Form |
| 52538 | Hiv-1 Protease Nl4-3 1X Mutant |
| 52539 | Hiv-1 Protease Nl4-3 3X Mutant in Complex With Inhibitor, Tl-3 |
| 58047 | Three-dimensional Structure of Aspartyl Protease From Human Immunodeficiency Virus Hiv-1 |
| 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 |
| 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 |