Structure of PDB 5p98 Chain A Binding Site BS02
Receptor Information
>5p98 Chain A (length=214) Species:
10116
(Rattus norvegicus) [
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GDTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMD
AVIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEMNPDYAAITQQ
MLNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDT
LLLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYM
KVVDGLEKAIYQGP
Ligand information
Ligand ID
77L
InChI
InChI=1S/C15H14FNO4/c16-11-3-1-9(2-4-11)10-7-12(14(20)13(19)8-10)15(21)17-5-6-18/h1-4,7-8,18-20H,5-6H2,(H,17,21)
InChIKey
ASGZSLFHJDBZNV-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
OCCNC(=O)c1cc(cc(O)c1O)c2ccc(F)cc2
OpenEye OEToolkits 1.7.6
c1cc(ccc1c2cc(c(c(c2)O)O)C(=O)NCCO)F
ACDLabs 12.01
c2c(c1ccc(F)cc1)cc(c(c2C(=O)NCCO)O)O
Formula
C15 H14 F N O4
Name
5-(4-fluorophenyl)-2,3-dihydroxy-N-(2-hydroxyethyl)benzamide
ChEMBL
DrugBank
ZINC
PDB chain
5p98 Chain A Residue 308 [
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Receptor-Ligand Complex Structure
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PDB
5p98
Crystal Structure of a COMT complex
Resolution
1.2 Å
Binding residue
(original residue number in PDB)
W38 M40 D141 H142 K144 N170 P174 E199
Binding residue
(residue number reindexed from 1)
W37 M39 D140 H141 K143 N169 P173 E198
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D141 K144 D169 N170 E199
Catalytic site (residue number reindexed from 1)
D140 K143 D168 N169 E198
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
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5p98
,
PDBe:5p98
,
PDBj:5p98
PDBsum
5p98
PubMed
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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