Structure of PDB 5p9v Chain A Binding Site BS03
Receptor Information
>5p9v Chain A (length=213) Species:
10116
(Rattus norvegicus) [
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DTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMDA
VIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQM
LNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDTL
LLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYMK
VVDGLEKAIYQGP
Ligand information
Ligand ID
7JM
InChI
InChI=1S/C14H11N3O2/c1-8-10(3-2-4-15-8)9-5-11-13(12(18)6-9)16-7-17-14(11)19/h2-7,18H,1H3,(H,16,17,19)
InChIKey
VPSVVKQCDRXIFW-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Cc1ncccc1c2cc(O)c3N=CNC(=O)c3c2
OpenEye OEToolkits 2.0.6
Cc1c(cccn1)c2cc3c(c(c2)O)N=CNC3=O
Formula
C14 H11 N3 O2
Name
6-(2-methylpyridin-3-yl)-8-oxidanyl-3~{H}-quinazolin-4-one;
8-hydroxy-6-(2-methylpyridin-3-yl)-3H-quinazolin-4-one
ChEMBL
DrugBank
ZINC
PDB chain
5p9v Chain A Residue 306 [
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Receptor-Ligand Complex Structure
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PDB
5p9v
Crystal Structure of a COMT complex
Resolution
1.04 Å
Binding residue
(original residue number in PDB)
W38 M40 D141 H142 N170 P174 E199
Binding residue
(residue number reindexed from 1)
W36 M38 D139 H140 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:5p9v
,
PDBe:5p9v
,
PDBj:5p9v
PDBsum
5p9v
PubMed
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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