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7N6X

Crystal structure of HIV-1 Protease multiple mutants PRS17 bound to inhibitor Amprenavir

Summary for 7N6X
Entry DOI10.2210/pdb7n6x/pdb
Related5T2E 5T2Z 6O54 6O57 6O5A 6O5X
DescriptorProtease, {3-[(4-AMINO-BENZENESULFONYL)-ISOBUTYL-AMINO]-1-BENZYL-2-HYDROXY-PROPYL}-CARBAMIC ACID TETRAHYDRO-FURAN-3-YL ESTER (3 entities in total)
Functional Keywordsdrug resistance, prs17, hydrolase
Biological sourceHuman immunodeficiency virus type 1 group M subtype B (isolate BRU/LAI) (HIV-1)
Total number of polymer chains2
Total formula weight22090.92
Authors
Burnaman, S.H.,Wang, Y.-F.,Weber, I.T. (deposition date: 2021-06-09, release date: 2021-09-08, Last modification date: 2023-10-18)
Primary citationBurnaman, S.H.,Kneller, D.W.,Wang, Y.F.,Kovalevsky, A.,Weber, I.T.
Revertant mutation V48G alters conformational dynamics of highly drug resistant HIV protease PRS17.
J.Mol.Graph.Model., 108:108005-108005, 2021
Cited by
PubMed: 34419931
DOI: 10.1016/j.jmgm.2021.108005
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.47 Å)
Structure validation

220472

数据于2024-05-29公开中

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