Structure of PDB 1eo9 Chain B Binding Site BS01
Receptor Information
>1eo9 Chain B (length=238) Species:
62977
(Acinetobacter baylyi ADP1) [
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IIWGAYAQRNTEDHPPAYAPGYKTSVLRSPKNALISIAETLSEVTAPHFS
ADKFGPKDNDLILNYAKDGLPIGERVIVHGYVRDQFGRPVKNALVEVWQA
NASGRYRHPNDQYIGAMDPNFGGCGRMLTDDNGYYVFRTIKPGPYPWRNR
INEWRPAHIHFSLIADGWAQRLISQFYFEGDTLIDSCPILKTIPSEQQRR
ALIALEDKSNFIEADSRCYRFDITLRGRRATYFENDLT
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
1eo9 Chain B Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1eo9
Structure of Acinetobacter strain ADP1 protocatechuate 3, 4-dioxygenase at 2.2 A resolution: implications for the mechanism of an intradiol dioxygenase.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
Y408 Y447 H460 H462
Binding residue
(residue number reindexed from 1)
Y106 Y145 H158 H160
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y408 Y447 R457 H460 H462
Catalytic site (residue number reindexed from 1)
Y106 Y145 R155 H158 H160
Enzyme Commision number
1.13.11.3
: protocatechuate 3,4-dioxygenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005506
iron ion binding
GO:0005515
protein binding
GO:0008199
ferric iron binding
GO:0016702
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
GO:0018578
protocatechuate 3,4-dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0009056
catabolic process
GO:0019619
3,4-dihydroxybenzoate catabolic process
GO:0042952
beta-ketoadipate pathway
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Molecular Function
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Biological Process
External links
PDB
RCSB:1eo9
,
PDBe:1eo9
,
PDBj:1eo9
PDBsum
1eo9
PubMed
10891075
UniProt
P20372
|PCXB_ACIAD Protocatechuate 3,4-dioxygenase beta chain (Gene Name=pcaH)
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