Structure of PDB 3nf8 Chain A Binding Site BS01
Receptor Information
>3nf8 Chain A (length=149) Species:
11676
(Human immunodeficiency virus 1) [
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SPGIWQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAG
RWPVKTVHTDNGSNFTSTTVKAACWWAGIKQEDGIPYNPQSQGVIESMNK
ELKKIIGQVRDQAEHLKTAVQMAVFIHNHKRKGYSAGERIVDIIATDIQ
Ligand information
Ligand ID
CDQ
InChI
InChI=1S/C18H14ClNO5/c19-12-2-3-13-11(7-12)8-15(21)20(13)9-10-1-4-14-17(16(10)18(22)23)25-6-5-24-14/h1-4,7H,5-6,8-9H2,(H,22,23)
InChIKey
KBLBOZBAVQRJSU-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)c2c(ccc1OCCOc12)CN4c3ccc(Cl)cc3CC4=O
CACTVS 3.370
OC(=O)c1c(CN2C(=O)Cc3cc(Cl)ccc23)ccc4OCCOc14
OpenEye OEToolkits 1.7.0
c1cc2c(cc1Cl)CC(=O)N2Cc3ccc4c(c3C(=O)O)OCCO4
Formula
C18 H14 Cl N O5
Name
6-[(5-chloro-2-oxo-2,3-dihydro-1H-indol-1-yl)methyl]-2,3-dihydro-1,4-benzodioxine-5-carboxylic acid
ChEMBL
DrugBank
ZINC
ZINC000066166930
PDB chain
3nf8 Chain A Residue 225 [
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Receptor-Ligand Complex Structure
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PDB
3nf8
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)
R107 P109 I204 D207 I208
Binding residue
(residue number reindexed from 1)
R51 P53 I144 D147 I148
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=3.00,IC50>1000uM
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
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Biological Process
External links
PDB
RCSB:3nf8
,
PDBe:3nf8
,
PDBj:3nf8
PDBsum
3nf8
PubMed
21602613
UniProt
P12497
|POL_HV1N5 Gag-Pol polyprotein (Gene Name=gag-pol)
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