Structure of PDB 6ng4 Chain A Binding Site BS03
Receptor Information
>6ng4 Chain A (length=414) Species:
9606
(Homo sapiens) [
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CPRFLKVKNWETEVVLTDTLHLKSTLETGCTEYICMGSIMHPEDVATKDQ
LFPLAKEFIDQYYSSIKRFGSKAHMERLEEVNKEIDTTSTYQLKDTELIY
GAKHAWRNASRCVGRIQWSKLQVFDARDCTTAHGMFNYICNHVKYATNKG
NLRSAITIFPQRTDGKHDFRVWNSQLIRYAGYKQPDGSTLGDPANVQFTE
ICIQQGWKPPRGRFDVLPLLLQANGNDPELFQIPPELVLEVPIRHPKFEW
FKDLGLKWYGLPAVSNMLLEIGGLEFSACPFSGWYMGTEIGVRDYCDNSR
YNILEEVAKKMNLDMRKTSSLWKDQALVEINIAVLYSFQSDKVTIVDHHS
ATESFIKHMENEYRCRGGCPADWVWIVPPMSGSITPVFHQEMLNYRLTPS
FEYQPDPWNTHVWK
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
6ng4 Chain A Residue 803 [
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Receptor-Ligand Complex Structure
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PDB
6ng4
Optimization of Blood-Brain Barrier Permeability with Potent and Selective Human Neuronal Nitric Oxide Synthase Inhibitors Having a 2-Aminopyridine Scaffold.
Resolution
1.776 Å
Binding residue
(original residue number in PDB)
C331 C336
Binding residue
(residue number reindexed from 1)
C30 C35
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C420 R423 W592 E597
Catalytic site (residue number reindexed from 1)
C112 R115 W284 E289
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
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Biological Process
External links
PDB
RCSB:6ng4
,
PDBe:6ng4
,
PDBj:6ng4
PDBsum
6ng4
PubMed
30802056
UniProt
P29475
|NOS1_HUMAN Nitric oxide synthase 1 (Gene Name=NOS1)
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