Structure of PDB 1m9r Chain A Binding Site BS03
Receptor Information
>1m9r Chain A (length=400) Species:
9606
(Homo sapiens) [
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KFPRVKNWEVGSITYDTLSAQAQQDGPCTPRRCLGSLVFPEQLLSQARDF
INQYYSSIKRSGSQAHEQRLQEVEAEVAATGTYQLRESELVFGAKQAWRN
APRCVGRIQWGKLQVFDARDCRSAQEMFTYICNHIKYATNRGNLRSAITV
FPQRCPGRGDFRIWNSQLVRYAGYRQQDGSVRGDPANVEITELCIQHGWT
PGNGRFDVLPLLLQAPDEPPELFLLPPELVLEVPLEHPTLEWFAALGLRW
YALPAVSNMLLEIGGLEFPAAPFSGWYMSTEIGTRNLCDPHRYNILEDVA
VCMDLDTRTTSSLWKDKAAVEINVAVLHSYQLAKVTIVDHHAATASFMKH
LENEQKARGGCPADWAWIVPPISGSLTPVFHQEMVNYFLSPAFRYQPDPW
Ligand information
Ligand ID
INE
InChI
InChI=1S/C7H4BrN3O2/c8-7-4-2-1-3-5(11(12)13)6(4)9-10-7/h1-3H,(H,9,10)
InChIKey
NFSTZPMYAZRZPC-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
[O-][N+](=O)c1cccc2c1nnc2Br
OpenEye OEToolkits 1.5.0
c1cc2c(c(c1)[N+](=O)[O-])[nH]nc2Br
CACTVS 3.341
[O-][N+](=O)c1cccc2c(Br)n[nH]c12
Formula
C7 H4 Br N3 O2
Name
3-BROMO-7-NITROINDAZOLE
ChEMBL
CHEMBL479014
DrugBank
DB01997
ZINC
ZINC000003870920
PDB chain
1m9r Chain A Residue 906 [
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Receptor-Ligand Complex Structure
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PDB
1m9r
Conformational Changes in Nitric Oxide Synthases Induced by Chlorzoxazone and Nitroindazoles: Crystallographic and Computational Analyses of Inhibitor Potency
Resolution
2.56 Å
Binding residue
(original residue number in PDB)
P334 F353 S354 G355 W356 Y357 M358 E361
Binding residue
(residue number reindexed from 1)
P254 F273 S274 G275 W276 Y277 M278 E281
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C184 R187 W356 E361
Catalytic site (residue number reindexed from 1)
C104 R107 W276 E281
Enzyme Commision number
1.14.13.39
: nitric-oxide synthase (NADPH).
Gene Ontology
Molecular Function
GO:0004517
nitric-oxide synthase activity
GO:0020037
heme binding
Biological Process
GO:0006809
nitric oxide biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1m9r
,
PDBe:1m9r
,
PDBj:1m9r
PDBsum
1m9r
PubMed
12437348
UniProt
P29474
|NOS3_HUMAN Nitric oxide synthase 3 (Gene Name=NOS3)
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