Structure of PDB 5oey Chain D Binding Site BS01
Receptor Information
>5oey Chain D (length=301) Species:
5664
(Leishmania major) [
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PTPTTLTQYIIKSQPGDFTLLMMAIQTSVKVIEKNIRRAGMKGMLGYAKL
DVISNIAFKAYLLSSTSVCVLGSEEEEQMIIAESGRRGDYLIFFDPLDGS
SNIDANVSVGSIWGVWRLPVIRMLKGTDMVSAGYAVYGSATNLVLTSGHG
VDGFTLDPNIGEFILTHPHISIPKKRSIYSVNEGNYGKWEPWFKEYIDYL
KMNKTTRYSARYIGSMVGDIHRTLLYGGIFCYPKDANQVEGKLRLLYEAA
PMAMIVEQAGGKAVGSNGRILEQSITRLHQRTPVYFGSRQEVDLCMAFRD
R
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
5oey Chain D Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
5oey
Structures of Leishmania Fructose-1,6-Bisphosphatase Reveal Species-Specific Differences in the Mechanism of Allosteric Inhibition.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
E97 D118 L120 D121
Binding residue
(residue number reindexed from 1)
E74 D95 L97 D98
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D74 E97 E98 D118 L120 D121 E284
Catalytic site (residue number reindexed from 1)
D51 E74 E75 D95 L97 D98 E248
Enzyme Commision number
3.1.3.11
: fructose-bisphosphatase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide 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: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:0020015
glycosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5oey
,
PDBe:5oey
,
PDBj:5oey
PDBsum
5oey
PubMed
28882541
UniProt
O97193
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