Structure of PDB 5k0c Chain B Binding Site BS01
Receptor Information
>5k0c Chain B (length=215) Species:
10116
(Rattus norvegicus) [
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GDTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMD
AVIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQ
MLNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDT
LLLEECGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYM
KVVDGLEKAIYQGPS
Ligand information
Ligand ID
6OZ
InChI
InChI=1S/C17H19N3S/c1-11-16(21-12(2)18-11)14-10-15(20-19-14)17(3,4)13-8-6-5-7-9-13/h5-10H,1-4H3,(H,19,20)
InChIKey
FAEGQXWWILYIST-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
Cc1sc(c2[nH]nc(c2)C(C)(C)c3ccccc3)c(C)n1
OpenEye OEToolkits 2.0.4
Cc1c(sc(n1)C)c2cc(n[nH]2)C(C)(C)c3ccccc3
ACDLabs 12.01
c1(ccccc1)C(c2nnc(c2)c3c(C)nc(C)s3)(C)C
Formula
C17 H19 N3 S
Name
2,4-dimethyl-5-[3-(2-phenylpropan-2-yl)-1H-pyrazol-5-yl]-1,3-thiazole
ChEMBL
CHEMBL4793611
DrugBank
ZINC
ZINC000584904693
PDB chain
5k0c Chain B Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
5k0c
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
1.95 Å
Binding residue
(original residue number in PDB)
G66 Y68 M89 E90 I91 A118 S119 H142 W143
Binding residue
(residue number reindexed from 1)
G65 Y67 M88 E89 I90 A117 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:5k0c
,
PDBe:5k0c
,
PDBj:5k0c
PDBsum
5k0c
PubMed
27685665
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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