1XL2
HIV-1 Protease in complex with pyrrolidinmethanamine
Summary for 1XL2
Entry DOI | 10.2210/pdb1xl2/pdb |
Related | 1AJX 1HVI 1XL5 |
Descriptor | PROTEASE RETROPEPSIN, CHLORIDE ION, N-BENZYL-2-(2,6-DIMETHYLPHENOXY)-N-[((3R,4S)-4-{[ISOBUTYL(PHENYLSULFONYL)AMINO]METHYL}PYRROLIDIN-3-YL)METHYL]ACETAMIDE, ... (5 entities in total) |
Functional Keywords | aspartyl protease; hiv protease; pyrrolidine inhibitor, hydrolase |
Biological source | Human immunodeficiency virus 1 |
Cellular location | Gag-Pol polyprotein: Host cell membrane ; Lipid-anchor. Matrix protein p17: Virion membrane; Lipid- anchor . Capsid protein p24: Virion . Nucleocapsid protein p7: Virion . Reverse transcriptase/ribonuclease H: Virion . Integrase: Virion : P03367 |
Total number of polymer chains | 2 |
Total formula weight | 22348.29 |
Authors | Boettcher, J.,Specker, E.,Heine, A.,Klebe, G. (deposition date: 2004-09-30, release date: 2005-06-07, Last modification date: 2023-08-23) |
Primary citation | Specker, E.,Boettcher, J.,Lilie, H.,Heine, A.,Schoop, A.,Muller, G.,Griebenow, N.,Klebe, G. An Old Target Revisited: Two New Privileged Skeletons and an Unexpected Binding Mode For HIV-Protease Inhibitors Angew.Chem.Int.Ed.Engl., 44:3140-3144, 2005 Cited by PubMed: 15822136DOI: 10.1002/anie.200462643 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.5 Å) |
Structure validation
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