Structure of PDB 5p9t Chain A Binding Site BS02
Receptor Information
>5p9t Chain A (length=213) Species:
10116
(Rattus norvegicus) [
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DTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMDA
VIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQM
LNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDTL
LLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYMK
VVDGLEKAIYQGP
Ligand information
Ligand ID
7JD
InChI
InChI=1S/C14H9FN2O2/c15-10-3-1-8(2-4-10)9-5-11-13(12(18)6-9)16-7-17-14(11)19/h1-7,18H,(H,16,17,19)
InChIKey
MVFBYXBGOWGDLX-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Oc1cc(cc2C(=O)NC=Nc12)c3ccc(F)cc3
OpenEye OEToolkits 2.0.6
c1cc(ccc1c2cc3c(c(c2)O)N=CNC3=O)F
Formula
C14 H9 F N2 O2
Name
6-(4-fluorophenyl)-8-oxidanyl-3~{H}-quinazolin-4-one;
6-(4-fluorophenyl)-8-hydroxy-3H-quinazolin-4-one
ChEMBL
DrugBank
ZINC
PDB chain
5p9t Chain A Residue 304 [
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Receptor-Ligand Complex Structure
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PDB
5p9t
Crystal Structure of a COMT complex
Resolution
1.24 Å
Binding residue
(original residue number in PDB)
W38 M40 D141 H142 N170 P174 L198 E199
Binding residue
(residue number reindexed from 1)
W36 M38 D139 H140 N168 P172 L196 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:5p9t
,
PDBe:5p9t
,
PDBj:5p9t
PDBsum
5p9t
PubMed
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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