Structure of PDB 3zt3 Chain A Binding Site BS01
Receptor Information
>3zt3 Chain A (length=149) Species:
12721
(Human immunodeficiency virus) [
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SPGIWQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAG
RWPVKTVHTDNGSNFTSTTVKAACWWAGIKQEDGIPYNPQSQGVIESMNK
ELKKIIGQVRDQAEHLKTAVQMAVFIHNHKRKGYSAGERIVDIIATDIQ
Ligand information
Ligand ID
ZT4
InChI
InChI=1S/C18H14O5/c19-14-8-10-3-1-2-4-12(10)13(14)7-11-5-6-15-17(23-9-22-15)16(11)18(20)21/h1-7,14,19H,8-9H2,(H,20,21)/b13-7+/t14-/m0/s1
InChIKey
SLQGUUWKGRSNCG-GUNGLEHYSA-N
SMILES
Software
SMILES
CACTVS 3.385
O[CH]1Cc2ccccc2C1=Cc3ccc4OCOc4c3C(O)=O
CACTVS 3.385
O[C@H]1Cc2ccccc2\C1=C/c3ccc4OCOc4c3C(O)=O
OpenEye OEToolkits 1.9.2
c1ccc2c(c1)CC(C2=Cc3ccc4c(c3C(=O)O)OCO4)O
ACDLabs 12.01
O=C(O)c1c(ccc2OCOc12)/C=C4\c3ccccc3CC4O
Formula
C18 H14 O5
Name
5-{(E)-[(2R)-2-HYDROXY-2,3-DIHYDRO-1H-INDEN-1-YLIDENE]METHYL}-1,3-BENZODIOXOLE-4-CARBOXYLIC ACID
ChEMBL
DrugBank
ZINC
ZINC000095920888
PDB chain
3zt3 Chain A Residue 1216 [
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Receptor-Ligand Complex Structure
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PDB
3zt3
Small Molecule Inhibitors of the Ledgf Site of Human Immunodeficiency Virus Integrase Identified by Fragment Screening and Structure Based Design.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
A169 E170 H171 T174 M178
Binding residue
(residue number reindexed from 1)
A113 E114 H115 T118 M122
Annotation score
1
Binding affinity
MOAD
: Kd=1435uM
PDBbind-CN
: -logKd/Ki=2.86,Kd=1375uM
Enzymatic activity
Enzyme Commision number
2.7.7.-
2.7.7.49
: RNA-directed DNA polymerase.
2.7.7.7
: DNA-directed DNA polymerase.
3.1.-.-
3.1.13.2
: exoribonuclease H.
3.1.26.13
: retroviral ribonuclease H.
3.4.23.16
: HIV-1 retropepsin.
Gene Ontology
Molecular Function
GO:0003676
nucleic acid binding
Biological Process
GO:0015074
DNA integration
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3zt3
,
PDBe:3zt3
,
PDBj:3zt3
PDBsum
3zt3
PubMed
22808106
UniProt
P12497
|POL_HV1N5 Gag-Pol polyprotein (Gene Name=gag-pol)
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