Structure of PDB 4fua Chain A Binding Site BS01
Receptor Information
>4fua Chain A (length=206) Species:
562
(Escherichia coli) [
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MERNKLARQIIDTCLEMTRLGLNQGTAGNVSVRYQDGMLITPTGIPYEKL
TESHIVFIDGNGKHEEGKLPSSEWRFHMAAYQSRPDANAVVHNHAVHCTA
VSILNRSIPAIHYMIAAAGGNSIPCAPYATFGTRELSEHVALALKNRKAT
LLQHHGLIACEVNLEKALWLAHEVEVLAQLYLTTLAITDPVPVLSDEEIA
VVLEKF
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
4fua Chain A Residue 216 [
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Receptor-Ligand Complex Structure
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PDB
4fua
Catalytic mechanism of the metal-dependent fuculose aldolase from Escherichia coli as derived from the structure.
Resolution
2.43 Å
Binding residue
(original residue number in PDB)
H92 H94 H155
Binding residue
(residue number reindexed from 1)
H92 H94 H155
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E73 H92 H94 Y113 A117 H155
Catalytic site (residue number reindexed from 1)
E73 H92 H94 Y113 A117 H155
Enzyme Commision number
4.1.2.17
: L-fuculose-phosphate aldolase.
Gene Ontology
Molecular Function
GO:0008270
zinc ion binding
GO:0008738
L-fuculose-phosphate aldolase activity
GO:0016829
lyase activity
GO:0016830
carbon-carbon lyase activity
GO:0016832
aldehyde-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0005996
monosaccharide metabolic process
GO:0006004
fucose metabolic process
GO:0019317
fucose catabolic process
GO:0019323
pentose catabolic process
GO:0019568
arabinose catabolic process
GO:0019571
D-arabinose catabolic process
GO:0042355
L-fucose catabolic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4fua
,
PDBe:4fua
,
PDBj:4fua
PDBsum
4fua
PubMed
8676381
UniProt
P0AB87
|FUCA_ECOLI L-fuculose phosphate aldolase (Gene Name=fucA)
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