Structure of PDB 5vjd Chain A Binding Site BS01
Receptor Information
>5vjd Chain A (length=343) Species:
83333
(Escherichia coli K-12) [
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SKIFDFVKPGVITGDDVQKVFQVAKENNFALPAVNCVGTDSINAVLETAA
KVKAPVIVQFSNGGASFIAGKGVKSDVPQGAAILGAISGAHHVHQMAEHY
GVPVILHTDHCAKKLLPWIDGLLDAGEKHFAATGKPLFSSHMIDLSEESL
QENIEICSKYLERMSKIGMTLEIELGCTGGYTQPEDVDYAYTELSKISPR
FTIAASFGNVHGVYKPGNVVLTPTILRDSQEYVSKKHNLPHNSLNFVFHG
GSGSTAQEIKDSVSYGVVKMNIDTDTQWATWEGVLNYYKANEAYLQGQLG
NPKGEDQPNKKYYDPRVWLRAGQTSMIARLEKAFQELNAIDVL
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
5vjd Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5vjd
Active site remodeling during the catalytic cycle in metal-dependent fructose-1,6-bisphosphate aldolases.
Resolution
1.701 Å
Binding residue
(original residue number in PDB)
H110 H226 H264
Binding residue
(residue number reindexed from 1)
H110 H211 H249
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D109 H110 H226 H264 N286
Catalytic site (residue number reindexed from 1)
D109 H110 H211 H249 N271
Enzyme Commision number
4.1.2.13
: fructose-bisphosphate aldolase.
Gene Ontology
Molecular Function
GO:0004332
fructose-bisphosphate aldolase activity
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0016829
lyase activity
GO:0016832
aldehyde-lyase activity
GO:0042802
identical protein binding
GO:0042803
protein homodimerization 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:5vjd
,
PDBe:5vjd
,
PDBj:5vjd
PDBsum
5vjd
PubMed
29593097
UniProt
P0AB71
|ALF_ECOLI Fructose-bisphosphate aldolase class 2 (Gene Name=fbaA)
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