Structure of PDB 7cbr Chain A Binding Site BS02
Receptor Information
>7cbr Chain A (length=321) Species:
1648923
(Bacillus paralicheniformis) [
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KKKVALITTGGTIASRKTESGRLAAGAISGPELAEMCSLPEDVQIDVYPA
FQLPSMHITFQHLLELKQTVERVFQDGSYDGVVVTHGTDTLEETAYFLDL
TLQDERPVVVTGSQRAPEQQGTDAYTNIRHAVYTACSPDIKGAGTVVVFN
ERIFNARYVKKVHASNLQGFDVFGFGYLGIIDNDKVYVYQKPLKRDVHQL
QRPLPEVDIVKCYLDGDGKFIRAAVREGAAGIVLEGVGRGQVPPNMVGDI
EQALHQGVYIVITTSAEEGEVYTTYDMAGSSYDLAKKGVILGKDYDSKKA
RMKLAVLLASYEEGIKDKFCY
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
7cbr Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
7cbr
Structures of l-asparaginase from Bacillus licheniformis Reveal an Essential Residue for its Substrate Stereoselectivity.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
E268 D295
Binding residue
(residue number reindexed from 1)
E267 D294
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T13 L24 E36 T89 D90 N156 K162 T274 A279 G280 S282
Catalytic site (residue number reindexed from 1)
T12 L23 E35 T88 D89 N155 K161 T273 A278 G279 S281
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0004067
asparaginase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological Process
GO:0006520
amino acid metabolic process
GO:0006528
asparagine metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:7cbr
,
PDBe:7cbr
,
PDBj:7cbr
PDBsum
7cbr
PubMed
33371681
UniProt
A0A6I7U6Y2
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