Structure of PDB 1jsl Chain D Binding Site BS01
Receptor Information
>1jsl Chain D (length=324) Species:
556
(Dickeya chrysanthemi) [
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LPNIVILATGGTIAGSAATGTQTTGYKAGALGVDTLINAVPEVKKLANVK
GEQFSNMASENMTGDVVLKLSQRVNELLARDDVDGVVITHGTDTVEESAY
FLHLTVKSDKPVVFVAAMRPATAISADGPMNLLEAVRVAGDKQSRGRGVM
VVINDRIGSARYITKTNASTLDTFRANEEGYLGVIIGNRIYYQNRIDKLH
TTRSVFDVRGLTSLPKVDILYGYQDDPEYLYDAAIQHGVKGIVYAGMGAG
SVSVRGIAGMRKALEKGVVVMRSTRTGNGIVPPDEELPGLVSDSLNPAHA
RILLMLALTRTSDPKVIQEYFHTY
Ligand information
Ligand ID
DDO
InChI
InChI=1S/C6H13NO3/c7-5(6(9)10)3-1-2-4-8/h5,8H,1-4,7H2,(H,9,10)/t5-/m1/s1
InChIKey
OLUWXTFAPJJWPL-RXMQYKEDSA-N
SMILES
Software
SMILES
CACTVS 3.341
N[CH](CCCCO)C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCCCO
OpenEye OEToolkits 1.5.0
C(CCO)CC(C(=O)O)N
OpenEye OEToolkits 1.5.0
C(CCO)C[C@H](C(=O)O)N
CACTVS 3.341
N[C@H](CCCCO)C(O)=O
Formula
C6 H13 N O3
Name
6-HYDROXY-D-NORLEUCINE
ChEMBL
DrugBank
DB02233
ZINC
ZINC000002035148
PDB chain
1jsl Chain D Residue 2404 [
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Receptor-Ligand Complex Structure
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PDB
1jsl
Do bacterial L-asparaginases utilize a catalytic triad Thr-Tyr-Glu?
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
T15 Y29 A61 S62 E63 G94 T95 D96 A120
Binding residue
(residue number reindexed from 1)
T12 Y26 A58 S59 E60 G91 T92 D93 A117
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
T15 Y29 T95 D96 K168
Catalytic site (residue number reindexed from 1)
T12 Y26 T92 D93 K165
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:1jsl
,
PDBe:1jsl
,
PDBj:1jsl
PDBsum
1jsl
PubMed
11755201
UniProt
P06608
|ASPG_DICCH L-asparaginase (Gene Name=ansB)
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