Structure of PDB 1gvf Chain A Binding Site BS02
Receptor Information
>1gvf Chain A (length=273) Species:
562
(Escherichia coli) [
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SIISTKYLLQDAQANGYAVPAFNIHNAETIQAILEVCSEMRSPVILAGTP
GTFKHIALEEIYALCSAYSTTYNMPLALHLDHHESLDDIRRKVHAGVRSA
MIDGSHFPFAENVKLVKSVVDFCHSQDCSVEAELGRLGSAFLTDPQEAKR
FVELTGVDSLAVAIGTAHGLYSKTPKIDFQRLAEIREVVDVPLVLHGASD
VPDEFVRRTIELGVTKVNVATELKIAFAGAVKAWFAENPQGNDPRYYMRV
GMDAMKEVVRNKINVCGSANRIS
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
1gvf Chain A Residue 288 [
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Receptor-Ligand Complex Structure
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PDB
1gvf
Structure of Tagatose-1,6-Bisphosphate Aldolase; Insight Into Chiral Discrimination, Mechanism and Specificity of Class II Aldolases
Resolution
1.45 Å
Binding residue
(original residue number in PDB)
H83 H180 H208
Binding residue
(residue number reindexed from 1)
H82 H168 H196
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D82 H83 H180 H208 N230
Catalytic site (residue number reindexed from 1)
D81 H82 H168 H196 N218
Enzyme Commision number
4.1.2.40
: tagatose-bisphosphate aldolase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0009025
tagatose-bisphosphate aldolase activity
GO:0016829
lyase activity
GO:0016832
aldehyde-lyase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0051289
protein homotetramerization
GO:2001059
D-tagatose 6-phosphate catabolic process
Cellular Component
GO:0005829
cytosol
GO:0032991
protein-containing complex
GO:1902494
catalytic complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1gvf
,
PDBe:1gvf
,
PDBj:1gvf
PDBsum
1gvf
PubMed
11940603
UniProt
P0AB74
|KBAY_ECOLI D-tagatose-1,6-bisphosphate aldolase subunit KbaY (Gene Name=kbaY)
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