Structure of PDB 2q8m Chain A Binding Site BS03
Receptor Information
>2q8m Chain A (length=310) Species:
621
(Shigella boydii) [
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MKTLGEFIVEKQHEFSHATGELTALLSAIKLGAKIIHRDINKAGLFANEK
LKAALKARDIVAGIASEEEDEIVVFEGCEHAKYVVLMDPLDGSSNIDVNV
SVGTIFSIYRRVTPVGTPVTEEDFLQPGNKQVAAGYVVYGSSTMLVYTTG
CGVHAFTYDPSLGVFCLCQERMRFPEKGKTYSINEGNYIKFPNGVKKYIK
FCQEEDKSTNRPYTSRYIGSLVADFHRNLLKGGIYLYPSTASHPDGKLRL
LYECNPMAFLAEQAGGKASDGKERILDIIPETLHQRRSFFVGNDHMVEDV
ERFIREFPDA
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
2q8m Chain A Residue 347 [
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Receptor-Ligand Complex Structure
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PDB
2q8m
Structure of Inhibited Fructose-1,6-bisphosphatase from Escherichia coli: DISTINCT ALLOSTERIC INHIBITION SITES FOR AMP AND GLUCOSE 6-PHOSPHATE AND THE CHARACTERIZATION OF A GLUCONEOGENIC SWITCH.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
E89 D110 L112
Binding residue
(residue number reindexed from 1)
E67 D88 L90
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E89 E90 D110 L112 D113 E275
Catalytic site (residue number reindexed from 1)
E67 E68 D88 L90 D91 E253
Enzyme Commision number
3.1.3.11
: fructose-bisphosphatase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0000287
magnesium ion binding
GO:0016787
hydrolase activity
GO:0016791
phosphatase activity
GO:0042132
fructose 1,6-bisphosphate 1-phosphatase activity
GO:0042578
phosphoric ester hydrolase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0005986
sucrose biosynthetic process
GO:0006000
fructose metabolic process
GO:0006002
fructose 6-phosphate metabolic process
GO:0006094
gluconeogenesis
GO:0030388
fructose 1,6-bisphosphate metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0032991
protein-containing complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2q8m
,
PDBe:2q8m
,
PDBj:2q8m
PDBsum
2q8m
PubMed
17567577
UniProt
P0A993
|F16PA_ECOLI Fructose-1,6-bisphosphatase class 1 (Gene Name=fbp)
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