Structure of PDB 1gqw Chain B Binding Site BS01
Receptor Information
>1gqw Chain B (length=273) Species:
562
(Escherichia coli) [
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ERLSITPLGPYIGAQISGADRPLSDNQFEQLYHAVLRHQVVFLRDQAITP
QQQRALAQRFGELHIHPVYPHAEGVDEIIVLDTHNDNPPDNDNWHTDVTF
IETPPAGAILAAKELPSTGGDTLWTSGIAAYEALSVPFRQLLSGLRAEHD
FRKSFPEYKYEHQRWREAVAKNPPLLHPVVRTHPVSGKQALFVNEGFTTR
IVDVSEKESEALLSFLFAHITKPEFQVRWRWQPNDIAIWDNRVTQHYANA
DYLPQRRIMHRATILGDKPFYRA
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
1gqw Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1gqw
X-Ray Crystal Structure of Escherichia Coli Taurine/Alpha-Ketoglutarate Dioxygenase Complexed to Ferrous Iron and Substrates
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
H99 D101 H255
Binding residue
(residue number reindexed from 1)
H95 D97 H246
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H99 D101 H255 R270
Catalytic site (residue number reindexed from 1)
H95 D97 H246 R261
Enzyme Commision number
1.14.11.17
: taurine dioxygenase.
Gene Ontology
Molecular Function
GO:0000908
taurine dioxygenase activity
GO:0008198
ferrous iron binding
GO:0016491
oxidoreductase activity
GO:0031418
L-ascorbic acid binding
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0006790
sulfur compound metabolic process
GO:0019529
taurine catabolic process
GO:0051289
protein homotetramerization
Cellular Component
GO:0005737
cytoplasm
GO:1990205
taurine dioxygenase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1gqw
,
PDBe:1gqw
,
PDBj:1gqw
PDBsum
1gqw
PubMed
11955067
UniProt
P37610
|TAUD_ECOLI Alpha-ketoglutarate-dependent taurine dioxygenase (Gene Name=tauD)
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