Structure of PDB 5lqj Chain B Binding Site BS01
Receptor Information
>5lqj Chain B (length=214) Species:
10116
(Rattus norvegicus) [
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DTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMDA
VIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQM
LNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDTL
LLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYMK
VVDGLEKAIYQGPS
Ligand information
Ligand ID
72N
InChI
InChI=1S/C12H13N3/c1-9-13-14-12(10-7-8-10)15(9)11-5-3-2-4-6-11/h2-6,10H,7-8H2,1H3
InChIKey
NNSGFXSZQIRXDG-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Cc1nnc(C2CC2)n1c3ccccc3
OpenEye OEToolkits 2.0.5
Cc1nnc(n1c2ccccc2)C3CC3
Formula
C12 H13 N3
Name
3-cyclopropyl-5-methyl-4-phenyl-1,2,4-triazole
ChEMBL
DrugBank
ZINC
ZINC000584905100
PDB chain
5lqj Chain B Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5lqj
Crystal Structure of COMT in complex with 3-cyclopropyl-5-methyl-4-phenyl-1,2,4-triazole
Resolution
2.41 Å
Binding residue
(original residue number in PDB)
L61 R85 L87 T113 Y130 V132 L135
Binding residue
(residue number reindexed from 1)
L59 R83 L85 T111 Y128 V130 L133
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:5lqj
,
PDBe:5lqj
,
PDBj:5lqj
PDBsum
5lqj
PubMed
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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