Structure of PDB 5pa3 Chain A Binding Site BS02
Receptor Information
>5pa3 Chain A (length=213) Species:
10116
(Rattus norvegicus) [
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DTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMDA
VIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQM
LNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDTL
LLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYMK
VVDGLEKAIYQGP
Ligand information
Ligand ID
7JV
InChI
InChI=1S/C16H14N2O3/c1-21-8-10-4-2-3-5-12(10)11-6-13-15(14(19)7-11)17-9-18-16(13)20/h2-7,9,19H,8H2,1H3,(H,17,18,20)
InChIKey
CBWCDEQPQXXGLJ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.6
COCc1ccccc1c2cc3c(c(c2)O)NC=NC3=O
CACTVS 3.385
COCc1ccccc1c2cc(O)c3NC=NC(=O)c3c2
Formula
C16 H14 N2 O3
Name
6-[2-(methoxymethyl)phenyl]-8-oxidanyl-1~{H}-quinazolin-4-one;
8-hydroxy-6-[2-(methoxymethyl)phenyl]-3H-quinazolin-4-one
ChEMBL
DrugBank
ZINC
PDB chain
5pa3 Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5pa3
Crystal Structure of a COMT complex
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
W38 M40 D141 H142 W143 N170 P174 E199
Binding residue
(residue number reindexed from 1)
W36 M38 D139 H140 W141 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:5pa3
,
PDBe:5pa3
,
PDBj:5pa3
PDBsum
5pa3
PubMed
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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