Structure of PDB 1hg0 Chain A Binding Site BS01
Receptor Information
>1hg0 Chain A (length=327) Species:
556
(Dickeya chrysanthemi) [
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ADKLPNIVILATGGTIAGSAATGTQTTGYKAGALGVDTLINAVPEVKKLA
NVKGEQFSNMASENMTGDVVLKLSQRVNELLARDDVDGVVITHGTDTVEE
SAYFLHLTVKSDKPVVFVAAMRPATAISADGPMNLLEAVRVAGDKQSRGR
GVMVVINDRIGSARYITKTNASTLDTFRANEEGYLGVIIGNRIYYQNRID
KLHTTRSVFDVRGLTSLPKVDILYGYQDDPEYLYDAAIQHGVKGIVYAGM
GAGSVSVRGIAGMRKALEKGVVVMRSTRTGNGIVPPDEELPGLVSDSLNP
AHARILLMLALTRTSDPKVIQEYFHTY
Ligand information
Ligand ID
SIN
InChI
InChI=1S/C4H6O4/c5-3(6)1-2-4(7)8/h1-2H2,(H,5,6)(H,7,8)
InChIKey
KDYFGRWQOYBRFD-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
OC(=O)CCC(O)=O
OpenEye OEToolkits 1.7.0
C(CC(=O)O)C(=O)O
ACDLabs 12.01
O=C(O)CCC(=O)O
Formula
C4 H6 O4
Name
SUCCINIC ACID
ChEMBL
CHEMBL576
DrugBank
DB00139
ZINC
ZINC000000895030
PDB chain
1hg0 Chain A Residue 350 [
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Receptor-Ligand Complex Structure
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PDB
1hg0
Stuctural Basis for the Activity and Substrate Specificity of Erwinia Chrysanthemi L-Asparaginase
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
T15 A61 S62 G94 T95 D96
Binding residue
(residue number reindexed from 1)
T15 A61 S62 G94 T95 D96
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T15 Y29 T95 D96 K168
Catalytic site (residue number reindexed from 1)
T15 Y29 T95 D96 K168
Enzyme Commision number
3.5.1.1
: asparaginase.
Gene Ontology
Molecular Function
GO:0004067
asparaginase activity
GO:0016787
hydrolase activity
Biological Process
GO:0006520
amino acid metabolic process
GO:0006528
asparagine metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1hg0
,
PDBe:1hg0
,
PDBj:1hg0
PDBsum
1hg0
PubMed
11341830
UniProt
P06608
|ASPG_DICCH L-asparaginase (Gene Name=ansB)
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