Structure of PDB 3ctl Chain B Binding Site BS02
Receptor Information
>3ctl Chain B (length=219) Species:
562
(Escherichia coli) [
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MKISPSLMCMDLLKFKEQIEFIDSHADYFHIDIMDGHFVPNLTLSPFFVS
QVKKLATKPLDCHLMVTRPQDYIAQLARAGADFITLHPETINGQAFRLID
EIRRHDMKVGLILNPETPVEAMKYYIHKADKITVMTVDPGFAGQPFIPEM
LDKLAELKAWREREGLEYEIEVDGSCNQATYEKLMAAGADVFIVGTSGLF
NHAENIDEAWRIMTAQILA
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
3ctl Chain B Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
3ctl
Structural basis for substrate specificity in phosphate binding (beta/alpha)8-barrels: D-allulose 6-phosphate 3-epimerase from Escherichia coli K-12.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
H30 D32 H63 D173
Binding residue
(residue number reindexed from 1)
H30 D32 H63 D173
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S6 H30 D32 M34 H63 M65 M135 D173
Catalytic site (residue number reindexed from 1)
S6 H30 D32 M34 H63 M65 M135 D173
Enzyme Commision number
5.1.3.-
Gene Ontology
Molecular Function
GO:0004750
D-ribulose-phosphate 3-epimerase activity
GO:0016853
isomerase activity
GO:0016857
racemase and epimerase activity, acting on carbohydrates and derivatives
GO:0034700
allulose 6-phosphate 3-epimerase activity
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0009052
pentose-phosphate shunt, non-oxidative branch
GO:0019316
D-allose 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:3ctl
,
PDBe:3ctl
,
PDBj:3ctl
PDBsum
3ctl
PubMed
18700786
UniProt
P32719
|ALSE_ECOLI D-allulose-6-phosphate 3-epimerase (Gene Name=alsE)
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