Structure of PDB 4osy Chain B Binding Site BS02
Receptor Information
>4osy Chain B (length=295) Species:
9606
(Homo sapiens) [
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HMNPIVVVHGGGAGPISKDRKERVHQGMVRAATVGYGILREGGSAVDAVE
GAVVALEDDPEFNAGCGSVLNTNGEVEMDASIMDGKDLSAGAVSAVQCIA
NPIKLARLVMEKTPHCFLTDQGAAQFAAAMGVPEIPGEKLVTERNKKRLE
KEKHTVGAVALDCKGNVAYATSTGGIVNKMVGRVGDSPCLGAGGYADNDI
GAVSTTGHGESILKVNLARLTLFHIEQGKTVEEAADLSLGYMKSRVKGLG
GLIVVSKTGDWVAKWTSTSMPWAAAKDGKLHFGIDPDDTTITDLP
Ligand information
Ligand ID
GLY
InChI
InChI=1S/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5)
InChIKey
DHMQDGOQFOQNFH-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(C(=O)O)N
CACTVS 3.341
NCC(O)=O
ACDLabs 10.04
O=C(O)CN
Formula
C2 H5 N O2
Name
GLYCINE
ChEMBL
CHEMBL773
DrugBank
DB00145
ZINC
ZINC000004658552
PDB chain
4osy Chain B Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
4osy
Free glycine accelerates the autoproteolytic activation of human asparaginase.
Resolution
1.91 Å
Binding residue
(original residue number in PDB)
T168 R196 D199 G220 G222
Binding residue
(residue number reindexed from 1)
T155 R183 D186 G207 G209
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N62 T168 T186 R196 T219 G220
Catalytic site (residue number reindexed from 1)
N63 T155 T173 R183 T206 G207
Enzyme Commision number
3.4.19.5
: beta-aspartyl-peptidase.
3.5.1.1
: asparaginase.
Gene Ontology
Molecular Function
GO:0003948
N4-(beta-N-acetylglucosaminyl)-L-asparaginase activity
GO:0004067
asparaginase activity
GO:0008233
peptidase activity
GO:0008798
beta-aspartyl-peptidase activity
GO:0016787
hydrolase activity
Biological Process
GO:0006508
proteolysis
GO:0033345
asparagine catabolic process via L-aspartate
Cellular Component
GO:0001917
photoreceptor inner segment
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4osy
,
PDBe:4osy
,
PDBj:4osy
PDBsum
4osy
PubMed
23601642
UniProt
Q7L266
|ASGL1_HUMAN Isoaspartyl peptidase/L-asparaginase (Gene Name=ASRGL1)
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