Structure of PDB 5fhq Chain A Binding Site BS03
Receptor Information
>5fhq Chain A (length=213) Species:
10116
(Rattus norvegicus) [
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DTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMDA
VIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEMNPDYAAITQQM
LNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDTL
LLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYMK
VVDGLEKAIYQGP
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
5fhq Chain A Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
5fhq
Effects of Active-Site Modification and Quaternary Structure on the Regioselectivity of Catechol-O-Methyltransferase.
Resolution
1.63 Å
Binding residue
(original residue number in PDB)
D141 D169 N170
Binding residue
(residue number reindexed from 1)
D139 D167 N168
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5fhq
,
PDBe:5fhq
,
PDBj:5fhq
PDBsum
5fhq
PubMed
26797714
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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