Structure of PDB 6pa3 Chain A Binding Site BS02
Receptor Information
>6pa3 Chain A (length=334) Species:
83333
(Escherichia coli K-12) [
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MDHHHHHHLPNITILATGGTIAGGGDSATKSNYTVGKVGVENLVNAVPQL
KDIANVKGEQVVNIGSQDMNDNVWLTLAKKINTDCDKTDGFVITHGVDTM
EETAYFLDLTVKCDKPVVMVGAMRPSTSMSADGPFNLYNAVVTAADKASA
NRGVLVVMNDTVLDGRDVTTTNTTDVATFKSVNYGPLGYIHNGKIDYQRT
PARKHTSDTPFDVSKLNELPKVGIVYNYANASDLPAKALVDAGYDGIVSA
GVGNGNLYKSVFDTLATAAKTGTAVVRSSRVPTGATTQDAEVDDAKYGFV
ASGTLNPQKARVLLQLALTQTKDPQQIQQIFNQY
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
6pa3 Chain A Residue 405 [
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Receptor-Ligand Complex Structure
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PDB
6pa3
Geometric considerations support the double-displacement catalytic mechanism of l-asparaginase.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
H-4 H-2
Binding residue
(residue number reindexed from 1)
H4 H6
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T12 Y25 V89 D90 T162 E283
Catalytic site (residue number reindexed from 1)
T20 Y33 V97 D98 T170 E291
Enzyme Commision number
3.5.1.1
: asparaginase.
Gene Ontology
Molecular Function
GO:0004067
asparaginase activity
GO:0016787
hydrolase activity
GO:0042802
identical protein binding
Biological Process
GO:0006520
amino acid metabolic process
GO:0006528
asparagine metabolic process
GO:0006530
asparagine catabolic process
GO:0051289
protein homotetramerization
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0032991
protein-containing complex
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6pa3
,
PDBe:6pa3
,
PDBj:6pa3
PDBsum
6pa3
PubMed
31423681
UniProt
P00805
|ASPG2_ECOLI L-asparaginase 2 (Gene Name=ansB)
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