Structure of PDB 5k0l Chain C Binding Site BS02
Receptor Information
>5k0l Chain C (length=219) Species:
10116
(Rattus norvegicus) [
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GDTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMD
AVIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQ
MLNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDT
LLLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYM
KVVDGLEKAIYQGPSSPDK
Ligand information
Ligand ID
6P2
InChI
InChI=1S/C18H19N3OS/c1-11-17(23-12(2)19-11)15-10-16(21-20-15)18(8-9-18)13-4-6-14(22-3)7-5-13/h4-7,10H,8-9H2,1-3H3,(H,20,21)
InChIKey
ONGUVGXZNLWDHM-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.4
Cc1c(sc(n1)C)c2cc(n[nH]2)C3(CC3)c4ccc(cc4)OC
CACTVS 3.385
COc1ccc(cc1)C2(CC2)c3cc([nH]n3)c4sc(C)nc4C
ACDLabs 12.01
C2C(c1ccc(OC)cc1)(C2)c4cc(c3sc(nc3C)C)nn4
Formula
C18 H19 N3 O S
Name
5-{3-[1-(4-methoxyphenyl)cyclopropyl]-1H-pyrazol-5-yl}-2,4-dimethyl-1,3-thiazole
ChEMBL
CHEMBL4755152
DrugBank
ZINC
ZINC000584904761
PDB chain
5k0l Chain C Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5k0l
Design of Potent and Druglike Nonphenolic Inhibitors for Catechol O-Methyltransferase Derived from a Fragment Screening Approach Targeting the S-Adenosyl-l-methionine Pocket.
Resolution
2.02 Å
Binding residue
(original residue number in PDB)
M40 Y68 E90 I91 S119 H142 W143
Binding residue
(residue number reindexed from 1)
M39 Y67 E89 I90 S118 H141 W142
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:5k0l
,
PDBe:5k0l
,
PDBj:5k0l
PDBsum
5k0l
PubMed
27685665
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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