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3ZSZ

Small molecule inhibitors of the LEDGF site of HIV type 1 integrase identified by fragment screening and structure based drug design

Entity
Entity IDChain IDDescriptionTypeChain lengthFormula weightNumber of moleculesDB Name (Accession)Biological sourceDescriptive keywords
1A, BINTEGRASEpolymer16718395.82UniProt (Q76353)
Pfam (PF00665)
UniProt (by SIFTS) (P12497)
In PDB
HUMAN IMMUNODEFICIENCY VIRUS
2A, BSULFATE IONnon-polymer96.16Chemie (SO4)
3A, BACETATE IONnon-polymer59.05Chemie (ACT)
4A, B(R)-[2-[[(2S)-BUTAN-2-YL]CARBAMOYL]PHENYL]METHYL-[(4-CARBOXY-1,3-BENZODIOXOL-5-YL)METHYL]-METHYL-AZANIUMnon-polymer399.52Chemie (OM2)
5BCHLORIDE IONnon-polymer35.51Chemie (CL)
6waterwater18.096Chemie (HOH)
Sequence modifications
A, B: 56 - 212 (UniProt: Q76353)
PDBExternal DatabaseDetails
Met 46-expression tag
Gly 47-expression tag
Ser 48-expression tag
Ser 49-expression tag
His 50-expression tag
His 51-expression tag
His 52-expression tag
His 53-expression tag
His 54-expression tag
His 55-expression tag
Ser 56Cys 56engineered mutation
Asp 139Phe 139engineered mutation
His 185Phe 185engineered mutation
Sequence viewer
Contents of the asymmetric unit
PolymersNumber of chains2
Total formula weight36791.7
Non-Polymers*Number of molecules14
Total formula weight1706.0
All*Total formula weight38497.7
*Water molecules are not included.

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PDB entries from 2024-07-10

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