Structure of PDB 2qdg Chain D Binding Site BS01
Receptor Information
>2qdg Chain D (length=358) Species:
5665
(Leishmania mexicana) [
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MSRVTVLQSQLPAYNRLKTPYESELIATVKKLTTPGKGLLAADESIGSCT
KRFQPIGLSNTEEHRRQYRALMLEAEGFEQYISGVILHDETVGQKASNGQ
TFPEYLTARGVVPGIKTDMGLCPLLEGAEGEQMTEGLDGYVKRASAYYKK
GCRFCKWRNVYKIQNGTVSESAVRFNAETLARYAILSQMSGLVPIVEPEV
MIDGKHDIDTCQRVSEHVWREVVAALQRHGVIWEGCLLKPNMVVPGAESG
KTAAPEQVAHYTVMTLARTMPAMLPGVMFLSGGLSEVQASEYLNAINNSP
LPRPYFLSFSYARALQSSALKAWGGKESGLAAGRRAFLHRARMNSMAQLG
KYKRSDDD
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
2qdg Chain D Residue 2007 [
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Receptor-Ligand Complex Structure
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PDB
2qdg
Carboxy-Terminus Recruitment Induced by Substrate Binding in Eukaryotic Fructose Bis-phosphate Aldolases
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
E197 E199 R313
Binding residue
(residue number reindexed from 1)
E197 E199 R313
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D43 K156 E197 E199 K239 S310
Catalytic site (residue number reindexed from 1)
D43 K156 E197 E199 K239 S310
Enzyme Commision number
4.1.2.13
: fructose-bisphosphate aldolase.
Gene Ontology
Molecular Function
GO:0004332
fructose-bisphosphate aldolase activity
GO:0016829
lyase activity
Biological Process
GO:0006096
glycolytic process
GO:0030388
fructose 1,6-bisphosphate metabolic process
Cellular Component
GO:0005737
cytoplasm
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:2qdg
,
PDBe:2qdg
,
PDBj:2qdg
PDBsum
2qdg
PubMed
17661446
UniProt
Q9U5N6
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