Structure of PDB 5zol Chain J Binding Site BS01
Receptor Information
>5zol Chain J (length=221) Species:
83333
(Escherichia coli K-12) [
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SMELYLDTSDVVAVKALSRIFPLAGVTTNPSTIAAGKKPLDVVLPQLHEA
MGGQGRLFATVMATTAEGMVNDALKLRSIIADIVVKVPVTAEGLAAIKML
KAEGIPTLGTAVYGAAQGLLSALAGAEYVAPYVNRIDAQGGSGIQTVTDL
HQLLKMHAPQAKVLAASFKTPRQALDCLLAGCESITLPLDVAQQMQSYPA
VDAAVAKFEQDWQGAFGRTSI
Ligand information
Ligand ID
4Y8
InChI
InChI=1S/C3H6O2/c1-3(5)2-4/h4H,2H2,1H3
InChIKey
XLSMFKSTNGKWQX-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(C)CO
CACTVS 3.385
OpenEye OEToolkits 1.9.2
CC(=O)CO
Formula
C3 H6 O2
Name
1-hydroxypropan-2-one
ChEMBL
DrugBank
ZINC
ZINC000000895664
PDB chain
5zol Chain J Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5zol
The engineering of decameric d-fructose-6-phosphate aldolase A by combinatorial modulation of inter- and intra-subunit interactions.
Resolution
2.172 Å
Binding residue
(original residue number in PDB)
D6 N28 K85
Binding residue
(residue number reindexed from 1)
D7 N29 K86
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
P170 R171
Catalytic site (residue number reindexed from 1)
P171 R172
Enzyme Commision number
4.1.2.-
Gene Ontology
Molecular Function
GO:0016829
lyase activity
GO:0016832
aldehyde-lyase activity
GO:0042802
identical protein binding
GO:0097023
fructose 6-phosphate aldolase activity
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006000
fructose metabolic process
GO:0042182
ketone catabolic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5zol
,
PDBe:5zol
,
PDBj:5zol
PDBsum
5zol
PubMed
32519699
UniProt
P78055
|FSAA_ECOLI Fructose-6-phosphate aldolase 1 (Gene Name=fsaA)
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