Structure of PDB 2cl5 Chain A Binding Site BS04
Receptor Information
>2cl5 Chain A (length=214) Species:
10116
(Rattus norvegicus) [
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GDTKEQRILRYVQQNAKPGDPQSVLEAIDTYCTQKEWAMNVGDAKGQIMD
AVIREYSPSLVLELGAYCGYSAVRMARLLQPGARLLTMEMNPDYAAITQQ
MLNFAGLQDKVTILNGASQDLIPQLKKKYDVDTLDMVFLDHWKDRYLPDT
LLLEKCGLLRKGTVLLADNVIVPGTPDFLAYVRGSSSFECTHYSSYLEYM
KVVDGLEKAIYQGP
Ligand information
Ligand ID
BU3
InChI
InChI=1S/C4H10O2/c1-3(5)4(2)6/h3-6H,1-2H3/t3-,4-/m1/s1
InChIKey
OWBTYPJTUOEWEK-QWWZWVQMSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C[C@H]([C@@H](C)O)O
CACTVS 3.341
C[C@@H](O)[C@@H](C)O
ACDLabs 10.04
OC(C)C(O)C
OpenEye OEToolkits 1.5.0
CC(C(C)O)O
CACTVS 3.341
C[CH](O)[CH](C)O
Formula
C4 H10 O2
Name
(R,R)-2,3-BUTANEDIOL
ChEMBL
DrugBank
ZINC
ZINC000000901616
PDB chain
2cl5 Chain A Residue 1219 [
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Receptor-Ligand Complex Structure
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PDB
2cl5
Comparative Study of Ortho- and Meta-Nitrated Inhibitors of Catechol-O-Methyltransferase: Interactions with the Active Site and Regioselectivity of O-Methylation.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
W143 K144
Binding residue
(residue number reindexed from 1)
W142 K143
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:2cl5
,
PDBe:2cl5
,
PDBj:2cl5
PDBsum
2cl5
PubMed
16618795
UniProt
P22734
|COMT_RAT Catechol O-methyltransferase (Gene Name=Comt)
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