Structure of PDB 5k0l Chain A Binding Site BS02
Receptor Information
>5k0l Chain A (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 A 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 G66 Y68 M89 E90 I91 S119 H142 W143
Binding residue
(residue number reindexed from 1)
M39 G65 Y67 M88 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
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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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