Structure of PDB 3nf6 Chain A Binding Site BS02
Receptor Information
>3nf6 Chain A (length=149) Species:
11676
(Human immunodeficiency virus 1) [
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SPGIWQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAG
RWPVKTVHTDNGSNFTSTTVKAACWWAGIKQEDGIPYNPQSQGVIESMNK
ELKKIIGQVRDQAEHLKTAVQMAVFIHNHKRKGYSAGERIVDIIATDIQ
Ligand information
Ligand ID
IMV
InChI
InChI=1S/C17H13NO5/c19-14-7-10-3-1-2-4-12(10)18(14)8-11-5-6-13-16(23-9-22-13)15(11)17(20)21/h1-6H,7-9H2,(H,20,21)
InChIKey
WSADZPAZSYSTNO-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C2N(c1ccccc1C2)Cc3ccc4OCOc4c3C(=O)O
CACTVS 3.370
OC(=O)c1c(CN2C(=O)Cc3ccccc23)ccc4OCOc14
OpenEye OEToolkits 1.7.0
c1ccc2c(c1)CC(=O)N2Cc3ccc4c(c3C(=O)O)OCO4
Formula
C17 H13 N O5
Name
5-[(2-oxo-2,3-dihydro-1H-indol-1-yl)methyl]-1,3-benzodioxole-4-carboxylic acid
ChEMBL
CHEMBL1738817
DrugBank
ZINC
ZINC000066156784
PDB chain
3nf6 Chain A Residue 230 [
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Receptor-Ligand Complex Structure
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PDB
3nf6
Structural basis for a new mechanism of inhibition of HIV-1 integrase identified by fragment screening and structure-based design
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
V79 G82 V150 M154 E157 H183
Binding residue
(residue number reindexed from 1)
V23 G26 V94 M98 E101 H127
Annotation score
1
Binding affinity
MOAD
: ic50=295uM
PDBbind-CN
: -logKd/Ki=3.53,IC50=295uM
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:3nf6
,
PDBe:3nf6
,
PDBj:3nf6
PDBsum
3nf6
PubMed
21602613
UniProt
P12497
|POL_HV1N5 Gag-Pol polyprotein (Gene Name=gag-pol)
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