CHEBI:16015
ChEBI
30572
ChemSpider
C4H4O5
Oxalacetic acid
132.00587
SMP0002304
SMPDB
937
ChemSpider
2.0
C00152
KEGG Compound
C00036
KEGG Compound
6267
PubChem-compound
328-50-7
CAS
AMP
BioCyc
Water
Adenosine monophosphate
1.0
Asparagine synthetase [glutamine-hydrolyzing] 2
SMILES
O
C10H14N5O7P
Adenosine monophosphate
347.06308
50
ChemSpider
HMDB0000250
HMDB
SMILES
[O-]P([O-])(=O)OP([O-])([O-])=O
14000-31-8
CAS
L-asparaginase 1
CHEBI:16027
ChEBI
HMDB0000538
HMDB
CHEBI:17196
ChEBI
OXALACETIC_ACID
BioCyc
ATP
BioCyc
asparaginase
C00049
KEGG Compound
5961
PubChem-compound
1.0
H4N
Ammonium
18.034374
56-85-9
CAS
L-Aspartic acid
328-42-7
CAS
HMDB0000148
HMDB
51
PubChem-compound
14798-03-9
CAS
559142
ChemSpider
1.0
2.0
1.0
Oxoglutaric acid
CHEBI:15422
ChEBI
SMP0002206
SMPDB
5746
ChemSpider
P38986
UniProt
5745
ChemSpider
5742
ChemSpider
ASN
BioCyc
SMILES
OC(=O)CC(=O)C(O)=O
1038
PubChem-compound
7732-18-5
CAS
L-ASPARTATE
BioCyc
61-19-8
CAS
GO:0005829
GENE ONTOLOGY
SMILES
NC1=C2N=CN([C@@H]3O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1
56-86-0
CAS
C5H6O5
Oxoglutaric acid
146.02153
Aspartate aminotransferase, mitochondrial
C5H9NO4
L-Glutamic acid
147.05316
Water
33032
PubChem-compound
L-Glutamic acid
5858
ChemSpider
SMILES
[NH4+]
C10H16N5O13P3
Adenosine triphosphate
506.99576
Pyrophosphate
1.0
CHEBI:17053
ChEBI
Oxalacetic acid
SubPathwayOutput
SubPathwayInteraction110047
SubPathway110047Reaction
SubPathwayReaction
C00064
KEGG Compound
945
ChemSpider
1010
ChemSpider
Saccharomyces cerevisiae
6031
ChemSpider
1.0
HMDB0000045
HMDB
HMDB0000168
HMDB
PPI
BioCyc
Mitochondrion
1.0
962
PubChem-compound
4.0
Ammonium
1.0
2-KETOGLUTARATE
BioCyc
C5H10N2O3
L-Glutamine
146.06914
Q01802
UniProt
HMDB0000208
HMDB
Cytosol
aspartate transaminase
asparagine synthetase A
218
ChemSpider
1.0
C00080
KEGG Compound
Asparagine synthetase [glutamine-hydrolyzing] 2
SMILES
OC(=O)CCC(=O)C(O)=O
Reaction6186
false
L-Glutamic acid + Oxalacetic acid → L-Aspartic acid + Oxoglutaric acid
LEFT_TO_RIGHT
Asparagine synthetase [glutamine-hydrolyzing] 1
ReactionCatalysis6136
ACTIVATION
1.0
CHEBI:30915
ChEBI
ReactionCatalysis6135
ACTIVATION
3.4.19.5
false
3.4.19.5
L-Asparagine + Water → Ammonium + L-Aspartic acid
LEFT_TO_RIGHT
ReactionCatalysis6134
ACTIVATION
L-asparaginase 1
Aspartate aminotransferase, mitochondrial
C4H8N2O3
L-Asparagine
132.0535
SMILES
N[C@@H](CCC(O)=O)C(O)=O
HMDB0002111
HMDB
ReactionCatalysis6138
ACTIVATION
ReactionCatalysis6137
ACTIVATION
CHEBI:15377
ChEBI
CHEBI:15378
ChEBI
SMILES
[H+]
Hydrogen Ion
6.3.5.4
false
6.3.5.4
Adenosine triphosphate + L-Aspartic acid + L-Glutamine + Water → Adenosine monophosphate + Hydrogen Ion + L-Asparagine + L-Glutamic acid + Pyrophosphate
LEFT_TO_RIGHT
6.3.5.4
false
6.3.5.4
Adenosine triphosphate + Ammonium + L-Aspartic acid → Adenosine monophosphate + Hydrogen Ion + L-Asparagine + Pyrophosphate
LEFT_TO_RIGHT
C00001
KEGG Compound
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
PW002274
PathWhiz
2.0
CHEBI:18361
ChEBI
C00002
KEGG Compound
asparagine synthetase B
1.0
1.0
HMDB0000223
HMDB
TCA Cycle
SubPathway
L-Aspartic acid
CHEBI:30744
ChEBI
GLN
BioCyc
GLT
BioCyc
Oxalacetic acid
C4H7NO4
L-Aspartic acid
133.0375
1.0
644102
PubChem-compound
1.0
L-Glutamine
4932
TAXONOMY
6083
PubChem-compound
44367445
PubChem-compound
Asparagine synthetase [glutamine-hydrolyzing] 1
16741146
PubChem-compound
1.0
C01342
KEGG Compound
CHEBI:28938
ChEBI
SMILES
N[C@@H](CCC(N)=O)C(O)=O
P49089
UniProt
C00013
KEGG Compound
SMILES
N[C@@H](CC(N)=O)C(O)=O
L-Aspartic acid
O7P2
Pyrophosphate
173.91193
CHEBI:18050
ChEBI
H2O
Water
18.010565
L-Asparagine
1.0
5957
PubChem-compound
HMDB0000191
HMDB
Ammonium
H
Hydrogen Ion
1.007825
HMDB0041827
HMDB
L-Asparagine
HMDB0059597
HMDB
P49090
UniProt
PW002377
PathWhiz
56-84-8
CAS
56-65-5
CAS
C00020
KEGG Compound
L-Glutamic acid
970
PubChem-compound
C00026
KEGG Compound
1.0
C00025
KEGG Compound
GO:0005739
GENE ONTOLOGY
1.0
Adenosine triphosphate
HMDB0000641
HMDB
Asparagine Metabolism
70-47-3
CAS
SMILES
N[C@@H](CC(O)=O)C(O)=O