Structure of PDB 1jaz Chain B Binding Site BS01
Receptor Information
>1jaz Chain B (length=305) Species:
562
(Escherichia coli) [
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LPNITILATGGTIAGNAVPQLKDIANVKGEQVVNIGSQDMNDNVWLTLAK
KINTDCDKTDGFVITHGTETMEETAYFLDLTVKCDKPVVMVGAMRPSTSM
SADGPFNLYNAVVTAADKASANRGVLVVMNDTVLDGRDVTKTNTTDVATF
KSVNYGPLGYIHNGKIDYQRTPARKHTSDTPFDVSKLNELPKVGIVYNYA
NASDLPAKALVDAGYDGIVSAGVGNGNLYKSVFDTLATAAKTGTAVVRSS
RVPTGATTQDAEVDDAKYGFVASGTLNPQKARVLLQLALTQTKDPQQIQQ
IFNQY
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
1jaz Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
1jaz
Crystal structure of active site mutant of antileukemic L-asparaginase reveals conserved zinc-binding site.
Resolution
2.27 Å
Binding residue
(original residue number in PDB)
D100 H197
Binding residue
(residue number reindexed from 1)
D79 H176
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T12 T89 E90 K162 E283
Catalytic site (residue number reindexed from 1)
T12 T68 E69 K141 E262
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:1jaz
,
PDBe:1jaz
,
PDBj:1jaz
PDBsum
1jaz
PubMed
25040257
UniProt
P00805
|ASPG2_ECOLI L-asparaginase 2 (Gene Name=ansB)
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