Structure of PDB 1m9r Chain A Binding Site BS04
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 903 [
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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)
W445 F460 H461 Q462 E463
Binding residue
(residue number reindexed from 1)
W365 F380 H381 Q382 E383
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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