Structure of PDB 3qm3 Chain D Binding Site BS01
Receptor Information
>3qm3 Chain D (length=344) Species:
197
(Campylobacter jejuni) [
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SNAMGVLDIVKAGVISGDELNKIYDYAKAEGFAIPAVNVVGTDSINAVLE
AAKKVNSPVIIQFSNGGAKFYAGKNCPNGEVLGAISGAKHVHLLAKAYGV
PVILHTDHAARKLLPWIDGLIEANAQYKKTHGQALFSSHMLDLSEESLEE
NLSTCEVYLQKLDALGVALEIELGCTGGTGIDNSKLYTQPEDVALAYERL
GKISDKFSIAASFGNVHGVSLQPEILKNSQKFVKDKFALNSDKPINFVFH
GGSGSELKDIKNAVSYGVIKMNIDTDTQWAFWDGVREYELKNRAYLQGQI
GNPEGDDKPNKKYYDPRVWLRSGEESMIKRLEIAFEDLNCINKN
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
3qm3 Chain D Residue 355 [
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Receptor-Ligand Complex Structure
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PDB
3qm3
1.85 Angstrom Resolution Crystal Structure of Fructose-bisphosphate Aldolase (Fba) from Campylobacter jejuni
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
H105 E169 H221 H260
Binding residue
(residue number reindexed from 1)
H108 E172 H217 H250
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D104 H105 H221 H260 N282
Catalytic site (residue number reindexed from 1)
D107 H108 H217 H250 N272
Enzyme Commision number
4.1.2.13
: fructose-bisphosphate aldolase.
Gene Ontology
Molecular Function
GO:0004332
fructose-bisphosphate aldolase activity
GO:0008270
zinc ion binding
GO:0016829
lyase activity
GO:0016832
aldehyde-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006094
gluconeogenesis
GO:0006096
glycolytic 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:3qm3
,
PDBe:3qm3
,
PDBj:3qm3
PDBsum
3qm3
PubMed
UniProt
Q0PAS0
|ALF_CAMJE Fructose-bisphosphate aldolase (Gene Name=fba)
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