Structure of PDB 7uan Chain A Binding Site BS03
Receptor Information
>7uan Chain A (length=412) Species:
10116
(Rattus norvegicus) [
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RFLKVKNWETDVVLTDTLHLKSTLETGCTEHICMGSIMLPSVATKDQLFP
LAKEFLDQYYSSIKRFGSKAHMDRLEEVNKEIESTSTYQLKDTELIYGAK
HAWRNASRCVGRIQWSKLQVFDARDCTTAHGMFNYICNHVKYATNKGNLR
SAITIFPQRTDGKHDFRVWNSQLIRYAGYKQPDGSTLGDPANVQFTEICI
QQGWKAPRGRFDVLPLLLQANGNDPELFQIPPELVLEVPIRHPKFDWFKD
LGLKWYGLPAVSNMLLEIGGLEFSACPFSGWYMGTEIGVRDYCDNSRYNI
LEEVAKKMDLDMRKTSSLWKDQALVEINIAVLYSFQSDKVTIVDHHSATE
SFIKHMENEYRCRGGCPADWVWIVPPMSGSITPVFHQEMLNYRLTPSFEY
QPDPWNTHVWKG
Ligand information
Ligand ID
M5L
InChI
InChI=1S/C14H21F2N3/c1-11-9-12(18-13(17)10-11)3-2-6-19-7-4-14(15,16)5-8-19/h9-10H,2-8H2,1H3,(H2,17,18)
InChIKey
QUDAAAGCJFIIKZ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Cc1cc(N)nc(CCCN2CCC(F)(F)CC2)c1
ACDLabs 12.01
Cc1cc(CCCN2CCC(F)(F)CC2)nc(N)c1
OpenEye OEToolkits 2.0.7
Cc1cc(nc(c1)N)CCCN2CCC(CC2)(F)F
Formula
C14 H21 F2 N3
Name
6-[3-(4,4-difluoropiperidin-1-yl)propyl]-4-methylpyridin-2-amine
ChEMBL
CHEMBL5182377
DrugBank
ZINC
PDB chain
7uan Chain A Residue 803 [
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Receptor-Ligand Complex Structure
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PDB
7uan
2-Aminopyridines with a shortened amino sidechain as potent, selective, and highly permeable human neuronal nitric oxide synthase inhibitors.
Resolution
1.6969 Å
Binding residue
(original residue number in PDB)
P565 V567 N569 F584 W587 E592
Binding residue
(residue number reindexed from 1)
P259 V261 N263 F278 W281 E286
Annotation score
1
Enzymatic activity
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
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:7uan
,
PDBe:7uan
,
PDBj:7uan
PDBsum
7uan
PubMed
35772285
UniProt
P29476
|NOS1_RAT Nitric oxide synthase 1 (Gene Name=Nos1)
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