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3SA3

Crystal structure of wild-type HIV-1 protease in complex with AG23

Summary for 3SA3
Entry DOI10.2210/pdb3sa3/pdb
Related3SA4 3SA5 3SA6 3SA7 3SA8 3SA9 3SAA 3SAB 3SAC
Related PRD IDPRD_000946
DescriptorProtease, ACETATE ION, PHOSPHATE ION, ... (5 entities in total)
Functional Keywordshiv-1 protease, drug resistance, drug design, protease inhibitors, aids, aspartyl protease, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains2
Total formula weight22506.49
Authors
Schiffer, C.A.,Nalam, M.N.L. (deposition date: 2011-06-02, release date: 2012-06-06, Last modification date: 2023-09-13)
Primary citationAltman, M.D.,Nalam, M.N.L.,Ali, A.,Cao, H.,Rana, T.M.,Schiffer, C.A.,Tidor, B.
Protease Inhibitors that protrude out from substrate envelope are more susceptible to developing drug resistance
To be Published,
Experimental method
X-RAY DIFFRACTION (1.65 Å)
Structure validation

218500

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