Structure of PDB 2fgv Chain B Binding Site BS01
Receptor Information
>2fgv Chain B (length=99) Species:
11676
(Human immunodeficiency virus 1) [
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PQITLWKRPLVTIRIGGQLKEALLDTGADDTVLEEMNLPGKWKPKMIGGI
GGFIKVRQYDQIPVEICGHKAIGTVLVGPNPVNIIGRNLLTQIGCTLNF
Ligand information
Ligand ID
QNC
InChI
InChI=1S/C10H7NO2/c12-10(13)9-6-5-7-3-1-2-4-8(7)11-9/h1-6H,(H,12,13)
InChIKey
LOAUVZALPPNFOQ-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)c1nc2ccccc2cc1
CACTVS 3.370
OC(=O)c1ccc2ccccc2n1
OpenEye OEToolkits 1.7.0
c1ccc2c(c1)ccc(n2)C(=O)O
Formula
C10 H7 N O2
Name
quinoline-2-carboxylic acid
ChEMBL
CHEMBL1160559
DrugBank
DB02428
ZINC
ZINC000000084153
PDB chain
2fgv Chain A Residue 508 [
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Receptor-Ligand Complex Structure
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PDB
2fgv
Role of invariant Thr80 in human immunodeficiency virus type 1 protease structure, function, and viral infectivity.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
R8 P81
Binding residue
(residue number reindexed from 1)
R8 P81
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=6.12,Kd=760nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D25 T26 G27
Catalytic site (residue number reindexed from 1)
D25 T26 G27
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:0004190
aspartic-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:2fgv
,
PDBe:2fgv
,
PDBj:2fgv
PDBsum
2fgv
PubMed
16809296
UniProt
P03369
|POL_HV1A2 Gag-Pol polyprotein (Gene Name=gag-pol)
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