Structure of PDB 5pa0 Chain A Binding Site BS02
Receptor Information
>5pa0 Chain A (length=213) Species:
10116
(Rattus norvegicus) [
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DTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMDA
VIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQM
LNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDTL
LLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYMK
VVDGLEKAIYQGP
Ligand information
Ligand ID
7JR
InChI
InChI=1S/C12H11NO2/c1-13-8-10(7-11(14)12(13)15)9-5-3-2-4-6-9/h2-8,14H,1H3
InChIKey
NDVZUSAEFIBAFV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.6
CN1C=C(C=C(C1=O)O)c2ccccc2
CACTVS 3.385
CN1C=C(C=C(O)C1=O)c2ccccc2
Formula
C12 H11 N O2
Name
1-methyl-3-oxidanyl-5-phenyl-pyridin-2-one;
3-hydroxy-1-methyl-5-phenylpyridin-2-one
ChEMBL
DrugBank
ZINC
PDB chain
5pa0 Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5pa0
Crystal Structure of a COMT complex
Resolution
1.26 Å
Binding residue
(original residue number in PDB)
X40 W143 K144 N170 P174 E199
Binding residue
(residue number reindexed from 1)
X38 W141 K142 N168 P172 E197
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D141 K144 D169 N170 E199
Catalytic site (residue number reindexed from 1)
D139 K142 D167 N168 E197
Enzyme Commision number
2.1.1.6
: catechol O-methyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0008171
O-methyltransferase activity
GO:0016206
catechol O-methyltransferase activity
Biological Process
GO:0006584
catecholamine metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:5pa0
,
PDBe:5pa0
,
PDBj:5pa0
PDBsum
5pa0
PubMed
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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