Structure of PDB 1bif Chain A Binding Site BS01
Receptor Information
>1bif Chain A (length=432) Species:
10116
(Rattus norvegicus) [
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CPTLIVMVGLPARGKTYISKKLTRYLNFIGVPTREFNVGQYRRDMVKTYK
SFEFFLPDNEEGLKIRKQCALAALNDVRKFLSEEGGHVAVFDATNTTRER
RAMIFNFGEQNGYKTFFVESICVDPEVIAANIVQVKLGSPDYVNRDSDEA
TEDFMRRIECYENSYESLDEEQDRDLSYIKIMDVGQSYVVNRVADHIQSR
IVYYLMNIHVTPRSIYLCRHGESELNLKGRIGGDPGLSPRGREFSKHLAQ
FISDQNIKDLKVFTSQMKRTIQTAEALSVPYEQFKVLNEIDAGVCEEMTY
EEIQDHYPLEFALRDQDKYRYRYPKGESYEDLVQRLEPVIMELERQENVL
VICHQAVMRCLLAYFLDKAAEELPYLKCPLHTVLKLTPVAYGCKVESIFL
NVAAVNTHRDRPQNVDISRPSEEALVTVPAHQ
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
1bif Chain A Residue 510 [
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Receptor-Ligand Complex Structure
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PDB
1bif
The crystal structure of the bifunctional enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase reveals distinct domain homologies.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
R255 H256 R305 E325 H390
Binding residue
(residue number reindexed from 1)
R219 H220 R269 E289 H354
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R255 H256 N262 R305 E325 H390
Catalytic site (residue number reindexed from 1)
R219 H220 N226 R269 E289 H354
Enzyme Commision number
2.7.1.105
: 6-phosphofructo-2-kinase.
3.1.3.46
: fructose-2,6-bisphosphate 2-phosphatase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003873
6-phosphofructo-2-kinase activity
GO:0004331
fructose-2,6-bisphosphate 2-phosphatase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016787
hydrolase activity
Biological Process
GO:0006000
fructose metabolic process
GO:0006003
fructose 2,6-bisphosphate metabolic process
GO:0016310
phosphorylation
GO:0046835
carbohydrate phosphorylation
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1bif
,
PDBe:1bif
,
PDBj:1bif
PDBsum
1bif
PubMed
8805587
UniProt
P25114
|F264_RAT 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4 (Gene Name=Pfkfb4)
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