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2AOE

crystal structure analysis of HIV-1 protease mutant V82A with a substrate analog CA-P2

Summary for 2AOE
Entry DOI10.2210/pdb2aoe/pdb
Related1A8K 1A94 2AOC 2AOD 2AOF 2AOG 2AOH 2AOI 2AOJ
Related PRD IDPRD_000349
DescriptorPOL POLYPROTEIN, SODIUM ION, CHLORIDE ION, ... (8 entities in total)
Functional Keywordshiv-1 protease, substrate analog, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHuman immunodeficiency virus type 1 (BH5 ISOLATE)
Cellular locationGag-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 : P04587
Total number of polymer chains2
Total formula weight22802.12
Authors
Tie, Y.,Boross, P.I.,Wang, Y.F.,Gaddis, L.,Liu, F.,Chen, X.,Tozser, J.,Harrison, R.W.,Weber, I.T. (deposition date: 2005-08-12, release date: 2006-01-17, Last modification date: 2023-08-23)
Primary citationTie, Y.,Boross, P.I.,Wang, Y.F.,Gaddis, L.,Liu, F.,Chen, X.,Tozser, J.,Harrison, R.W.,Weber, I.T.
Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 angstroms resolution crystal structures of HIV-1 protease mutants with substrate analogs.
Febs J., 272:5265-5277, 2005
Cited by
PubMed: 16218957
DOI: 10.1111/j.1742-4658.2005.04923.x
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.54 Å)
Structure validation

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