Structure of PDB 5uck Chain A Binding Site BS03
Receptor Information
>5uck Chain A (length=291) Species:
85962
(Helicobacter pylori 26695) [
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MLVKGNEILLKAHKEGYGVGAFNFVNFEMLNAIFEAGNEENSPLFIQASE
GAIKYMGIDMAVGMVKIMCERYPHIPVALHLDHGTTFESCEKAVKAGFTS
VMIDASHHAFEENLELTSKVVKMAHNAGVSVEAELGRLVNPKEAEQFVKE
SQVDYLAPAIGTSHGAFKFKGEPKLDFERLQEVKRLTNIPLVLHGASAIP
DNVRKSYLDAGGDLKGSKGVPFEFLQESVKGGINKVNTDTDLRIAFIAEV
RKVANEDKSQFDLRKFFSPAQLALKNVVKERMKLLGSANKI
Ligand information
Ligand ID
G3H
InChI
InChI=1S/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h1,3,5H,2H2,(H2,6,7,8)/t3-/m0/s1
InChIKey
LXJXRIRHZLFYRP-VKHMYHEASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C([C@H](C=O)O)OP(=O)(O)O
OpenEye OEToolkits 1.7.0
C(C(C=O)O)OP(=O)(O)O
CACTVS 3.370
O[CH](CO[P](O)(O)=O)C=O
ACDLabs 12.01
O=P(OCC(O)C=O)(O)O
CACTVS 3.370
O[C@H](CO[P](O)(O)=O)C=O
Formula
C3 H7 O6 P
Name
GLYCERALDEHYDE-3-PHOSPHATE
ChEMBL
CHEMBL1232918
DrugBank
DB02263
ZINC
ZINC000003869936
PDB chain
5uck Chain A Residue 405 [
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Receptor-Ligand Complex Structure
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PDB
5uck
Active site remodeling during the catalytic cycle in metal-dependent fructose-1,6-bisphosphate aldolases.
Resolution
1.782 Å
Binding residue
(original residue number in PDB)
S49 D82 H83 H180 D255 R259
Binding residue
(residue number reindexed from 1)
S49 D82 H83 H164 D239 R243
Annotation score
5
Enzymatic activity
Enzyme Commision number
4.1.2.13
: fructose-bisphosphate aldolase.
Gene Ontology
Molecular Function
GO:0004332
fructose-bisphosphate aldolase activity
GO:0008270
zinc ion binding
GO:0016829
lyase activity
GO:0016832
aldehyde-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006096
glycolytic process
GO:0030388
fructose 1,6-bisphosphate metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5uck
,
PDBe:5uck
,
PDBj:5uck
PDBsum
5uck
PubMed
29593097
UniProt
P56109
|ALF_HELPY Fructose-bisphosphate aldolase (Gene Name=fba)
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