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1XL2

HIV-1 Protease in complex with pyrrolidinmethanamine

Summary for 1XL2
Entry DOI10.2210/pdb1xl2/pdb
Related1AJX 1HVI 1XL5
DescriptorPROTEASE 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 Keywordsaspartyl protease; hiv protease; pyrrolidine inhibitor, hydrolase
Biological sourceHuman immunodeficiency virus 1
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 : P03367
Total number of polymer chains2
Total formula weight22348.29
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 citationSpecker, 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: 15822136
DOI: 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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