Structure of PDB 1mpy Chain D Binding Site BS01
Receptor Information
>1mpy Chain D (length=307) Species:
303
(Pseudomonas putida) [
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MNKGVMRPGHVQLRVLDMSKALEHYVELLGLIEMDRDDQGRVYLKAWTEV
DKFSLVLREADEPGMDFMGFKVVDEDALRQLERDLMAYGCAVEQLPAGEL
NSCGRRVRFQAPSGHHFELYADKEYTGKWGLNDVNPEAWPRDLKGMAAVR
FDHALMYGDELPATYDLFTKVLGFYLAEQVLDENGTRVAQFLSLSTKAHD
VAFIHHPEKGRLHHVSFHLETWEDLLRAADLISMTDTSIDIGPTRHGLTH
GKTIYFFDPSGNRNEVFCGGDYNYPDHKPVTWTTDQLGKAIFYHDRILNE
RFMTVLT
Ligand information
Ligand ID
FE2
InChI
InChI=1S/Fe/q+2
InChIKey
CWYNVVGOOAEACU-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Fe+2]
CACTVS 3.341
[Fe++]
Formula
Fe
Name
FE (II) ION
ChEMBL
DrugBank
DB14510
ZINC
PDB chain
1mpy Chain D Residue 308 [
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Receptor-Ligand Complex Structure
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PDB
1mpy
An archetypical extradiol-cleaving catecholic dioxygenase: the crystal structure of catechol 2,3-dioxygenase (metapyrocatechase) from Ppseudomonas putida mt-2.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
H153 H214 E265
Binding residue
(residue number reindexed from 1)
H153 H214 E265
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H153 H199 H214 H246 Y255 E265
Catalytic site (residue number reindexed from 1)
H153 H199 H214 H246 Y255 E265
Enzyme Commision number
1.13.11.2
: catechol 2,3-dioxygenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008198
ferrous iron binding
GO:0018577
catechol 2,3-dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0009056
catabolic process
GO:0042203
toluene catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1mpy
,
PDBe:1mpy
,
PDBj:1mpy
PDBsum
1mpy
PubMed
10368270
UniProt
P06622
|XYLE1_PSEPU Metapyrocatechase (Gene Name=xylE)
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