Structure of PDB 5uo6 Chain B Binding Site BS02
Receptor Information
>5uo6 Chain B (length=410) Species:
9606
(Homo sapiens) [
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PRFLKVKNWETEVVLTDTLHLKSTLETGCTEYICMGSIMHPSATKDQLFP
LAKEFIDQYYSSIKRFGSKAHMERLEEVNKEIDTTSTYQLKDTELIYGAK
HAWRNASRCVGRIQWSKLQVFDARDCTTAHGMFNYICNHVKYATNKGNLR
SAITIFPQRTDGKHDFRVWNSQLIRYAGYKQPDGSTLGDPANVQFTEICI
QQGWKPPRGRFDVLPLLLQANGNDPELFQIPPELVLEVPIRHPKFEWFKD
LGLKWYGLPAVSNMLLEIGGLEFSACPFSGWYMGTEIGVRDYCDNSRYNI
LEEVAKKMNLDMRKTSSLWKDQALVEINIAVLYSFQSDKVTIVDHHSATE
SFIKHMENEYRCRGGCPADWVWIVPPMSGSITPVFHQEMLNYRLTPSFEY
QPDPWNTHVW
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
5uo6 Chain A Residue 806 [
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Receptor-Ligand Complex Structure
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PDB
5uo6
Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors.
Resolution
1.96 Å
Binding residue
(original residue number in PDB)
C331 C336
Binding residue
(residue number reindexed from 1)
C29 C34
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C420 R423 W592 E597
Catalytic site (residue number reindexed from 1)
C109 R112 W281 E286
Enzyme Commision number
1.14.13.39
: nitric-oxide synthase (NADPH).
Gene Ontology
Molecular Function
GO:0004517
nitric-oxide synthase activity
Biological Process
GO:0006809
nitric oxide biosynthetic process
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Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5uo6
,
PDBe:5uo6
,
PDBj:5uo6
PDBsum
5uo6
PubMed
28422508
UniProt
P29475
|NOS1_HUMAN Nitric oxide synthase 1 (Gene Name=NOS1)
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