Structure of PDB 5lqn Chain A Binding Site BS01
Receptor Information
>5lqn Chain A (length=213) Species:
10116
(Rattus norvegicus) [
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DTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMDA
VIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEINPDCAAITQQM
LNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDTL
LLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYMK
VVDGLEKAIYQGP
Ligand information
Ligand ID
72O
InChI
InChI=1S/C14H12ClN3OS/c1-9-14(12-5-6-16-18-12)20-13(17-9)8-19-11-4-2-3-10(15)7-11/h2-7H,8H2,1H3,(H,16,18)
InChIKey
NTAUPEMIWLSANJ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.5
Cc1c(sc(n1)COc2cccc(c2)Cl)c3ccn[nH]3
CACTVS 3.385
Cc1nc(COc2cccc(Cl)c2)sc1c3[nH]ncc3
Formula
C14 H12 Cl N3 O S
Name
2-[(3-chloranylphenoxy)methyl]-4-methyl-5-(1~{H}-pyrazol-5-yl)-1,3-thiazole
ChEMBL
DrugBank
ZINC
ZINC000000121221
PDB chain
5lqn Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5lqn
Crystal Structure of COMT in complex with 2-[(3-chlorophenoxy)methyl]-4-methyl-5-(1H-pyrazol-5-yl)-1,3-thiazole
Resolution
1.72 Å
Binding residue
(original residue number in PDB)
G66 Y68 M89 E90 I91 A118 S119 Q120 H142 W143 R146
Binding residue
(residue number reindexed from 1)
G64 Y66 M87 E88 I89 A116 S117 Q118 H140 W141 R144
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:5lqn
,
PDBe:5lqn
,
PDBj:5lqn
PDBsum
5lqn
PubMed
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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