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4Q1X

Mutations Outside the Active Site of HIV-1 Protease Alter Enzyme Structure and Dynamic Ensemble of the Active Site to Confer Drug Resistance

Entity
Entity IDChain IDDescriptionTypeChain lengthFormula weightNumber of moleculesDB Name (Accession)Biological sourceDescriptive keywords
1A, B
(A, B)
ASPARTYL PROTEASEpolymer9910829.82UniProt (V5Y949)
Pfam (PF00077)
UniProt (by SIFTS) (P04585)
Human immunodeficiency virus 1
2C
(A)
(3R,3AS,6AR)-HEXAHYDROFURO[2,3-B]FURAN-3-YL(1S,2R)-3-[[(4-AMINOPHENYL)SULFONYL](ISOBUTYL)AMINO]-1-BENZYL-2-HYDROXYPROPYLCARBAMATEnon-polymer547.71Chemie (017)
3D
(A)
GLYCEROLnon-polymer92.11Chemie (GOL)
4E
(B)
PHOSPHATE IONnon-polymer95.01Chemie (PO4)
5F, G
(A, B)
waterwater18.093Chemie (HOH)
Sequence modifications
A, B: 1 - 99 (UniProt: V5Y949)
PDBExternal DatabaseDetails
Lys 7Gln 7engineered mutation
Ile 32Val 32engineered mutation
Sequence viewer
Contents of the asymmetric unit
PolymersNumber of chains2
Total formula weight21659.6
Non-Polymers*Number of molecules3
Total formula weight734.7
All*Total formula weight22394.4
*Water molecules are not included.

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PDB entries from 2025-06-18

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