C11H19NO11P
N-Acetylmuramate 6-phosphate
372.06958
6022
PubChem-compound
C2H4O2
Acetic acid
60.02113
C23H38N7O17P3S
Acetyl-CoA
809.1258
CHEBI:58690
ChEBI
Unknown
ReactionCatalysis173429
ACTIVATION
937
ChemSpider
3315
PubChem-compound
1.0
64-19-7
CAS
TransportCatalysis912
ACTIVATION
SMILES
O
HMDB0001062
HMDB
1.0
6133
PubChem-compound
Beta-hexosaminidase
Bifunctional protein GlmU
A6VF30
UniProt
HMDB0000538
HMDB
Phosphoglucosamine mutase
ATP
BioCyc
CHEBI:16264
ChEBI
C8H16NO9P
N-Acetyl-D-Glucosamine 6-Phosphate
301.05627
1.0
1.0
C3H6O3
D-Lactic acid
90.03169
528-04-1
CAS
6816
PubChem-compound
SubPathwayInteraction112324
SubPathway112324Reaction
SubPathwayReaction
SubPathwayInteraction112325
SubPathway112325Reaction
SubPathwayReaction
D-Lactic acid
ADP
BioCyc
1.0
ALPHA-D-GALACTOSYL-13-BETA-D-GALACTOS
BioCyc
N-Acetyl-D-Glucosamine 6-Phosphate
N-ACETYL-D-GLUCOSAMINE-6-P
BioCyc
1.0
D-LACTATE
BioCyc
N-acetylglucosamine-6-phosphate deacetylase
1.0
N-acetylmuramic acid 6-phosphate etherase
5742
ChemSpider
1038
PubChem-compound
C04256
KEGG Compound
GO:0005829
GENE ONTOLOGY
Lipopolysaccharide Biosynthesis
SubPathway
393240
ChemSpider
SMP0002044
SMPDB
8140645
ChemSpider
55423
ChemSpider
2.7.7.23
false
2.7.7.23
Acetyl-CoA + Glucosamine-1P → Coenzyme A + Hydrogen Ion + N-Acetyl-glucosamine 1-phosphate
LEFT_TO_RIGHT
1,6-anhydro-N-acetyl-β-muramate
PW000831
PathWhiz
CHEBI:15713
ChEBI
Acetyl-CoA
439174
PubChem-compound
SMILES
CC1=C(C=CC(=C1)C1=CC(C)=C(C=C1)N=NC1=C(O)C2=C(C=C1)C(=CC(=C2N)S(O)(=O)=O)S(O)(=O)=O)N=NC1=C(O)C2=C(C=C1)C(=CC(=C2N)S(O)(=O)=O)S(O)(=O)=O
GlcNAc-1,6-anhMurNAc-L-Ala-?-D-Glu-DAP-D-Ala
1010
ChemSpider
10326-41-7
CAS
Acetic acid
N-Acetyl-D-glucosamine
SMILES
CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N)[C@@H](O)C(=O)NCCC(=O)NCCS
GLUCOSAMINE-1P
BioCyc
440272
PubChem-compound
1.0
C8H15NO6
N-Acetyl-D-glucosamine
221.08994
C6H14NO8P
Glucosamine-1P
259.04572
1.0
388319
ChemSpider
Hydrogen Ion
Cytosol
C00357
KEGG Compound
Adenosine triphosphate
25202911
PubChem-compound
C9H15N2O15P3
Uridine triphosphate
483.96854
HMDB0001423
HMDB
HMDB0000215
HMDB
C17H27N3O17P2
Uridine diphosphate-N-acetylglucosamine
607.08154
Unknown
C00008
KEGG Compound
Anhydro-N-acetylmuramic acid kinase
N-acetyl-β-D-glucosamine(anhydrous)-N-acetylmuramate
Hydrogen Ion
C00001
KEGG Compound
PW002030
PathWhiz
C34H28N6O14S4
diphosphate
872.0546
C00002
KEGG Compound
ReactionCatalysis176876
ACTIVATION
HMDB0001311
HMDB
N-Acetyl-glucosamine 1-phosphate
ReactionCatalysis176877
ACTIVATION
SMILES
CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
ReactionCatalysis176878
ACTIVATION
ReactionCatalysis176879
ACTIVATION
C8H16NO9P
N-Acetyl-glucosamine 1-phosphate
301.05627
ReactionCatalysis176875
ACTIVATION
SMP0000851
SMPDB
C19H29N2O12
N-acetyl-β-D-glucosamine(anhydrous)-N-acetylmuramate
477.1726
1.0
1,6-Anhydro-N-acetylmuramic Acid Recycling
C00010
KEGG Compound
C00256
KEGG Compound
CHEBI:7125
ChEBI
Uridine diphosphate-N-acetylglucosamine
C00140
KEGG Compound
5957
PubChem-compound
HMDB0001206
HMDB
ReactionCatalysis176880
ACTIVATION
1.0
ReactionCatalysis176881
ACTIVATION
GO:0005620
GENE ONTOLOGY
ReactionCatalysis176882
ACTIVATION
Uridine triphosphate
Q02FS3
UniProt
H
Hydrogen Ion
1.007825
SMILES
[H][C@@](C)(N)C(O)=N[C@]([H])(CCC([O-])=O)C(O)=NCC([H])(CC[C@@]([H])(N)C(O)=O)C(O)=N[C@@]([H])(C)C(O)=O
N-Acetylmuramate 6-phosphate
56-65-5
CAS
fused N-acetylglucosamine-1-phosphate uridyltransferase and glucosamine-1-phosphate acetyltransferase
SubPathwayInput
Glucosamine-1P
440996
PubChem-compound
C00024
KEGG Compound
Adenosine diphosphate
C10H15N5O10P2
Adenosine diphosphate
427.02942
ACET
BioCyc
D-glucosamine 6-phosphate
SubPathwayInput
C6H14NO8P
D-glucosamine 6-phosphate
259.04572
1.0
C00033
KEGG Compound
N-ACETYL-D-GLUCOSAMINE-1-P
BioCyc
CHEBI:1146900
ChEBI
Water
1.0
4.0
Anhydro-N-acetylmuramic acid kinase
HMDB0001341
HMDB
C18H30N5O9
L-Ala-γ-D-Glu-DAP-D-Ala
460.20435
CHEBI:47968
ChEBI
CO-A
BioCyc
HMDB0001109
HMDB
C00043
KEGG Compound
72-89-9
CAS
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
Coenzyme A
1.0
C21H36N7O16P3S
Coenzyme A
767.11523
UTP
BioCyc
CHEBI:15784
ChEBI
389821
ChemSpider
CHEBI:15422
ChEBI
5903
ChemSpider
1.0
SMILES
C[C@@H](O[C@H]1[C@H](O)[C@H]2CO[C@H](O2)[C@@H]1N=C(C)[O-])C(O)=O
6557
ChemSpider
SMILES
CC(O)=O
SMILES
[H][C@@](N)(CCC[C@]([H])(N=C(O)CC[C@@]([H])(N=C(O)[C@]([H])(C)N=C(O)[C@@]([H])(C)O[C@@]1([H])[C@]([H])(O[C@]2([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]2([H])N=C(C)[O-])C2([H])COC([H])(O2)[C@]1([H])N=C(C)[O-])C(O)=O)C(O)=N[C@]([H])(C)C(O)=O)C(O)=O
SMILES
CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
7732-18-5
CAS
diphosphate
Reaction187023
false
1,6-anhydro-N-acetyl-β-muramate + Adenosine triphosphate + Water → Adenosine diphosphate + Hydrogen Ion + N-Acetylmuramate 6-phosphate
LEFT_TO_RIGHT
3.0
Reaction187024
false
N-Acetylmuramate 6-phosphate + Water ↔ D-Lactic acid + N-Acetyl-D-Glucosamine 6-Phosphate
REVERSIBLE
1.0
Reaction187025
false
N-Acetyl-D-Glucosamine 6-Phosphate + Water → Acetic acid + D-glucosamine 6-phosphate
LEFT_TO_RIGHT
Reaction187026
false
D-glucosamine 6-phosphate ↔ Glucosamine-1P
REVERSIBLE
HMDB0001367
HMDB
Reaction187027
false
Hydrogen Ion + N-Acetyl-glucosamine 1-phosphate + Uridine triphosphate → Uridine diphosphate-N-acetylglucosamine + diphosphate
LEFT_TO_RIGHT
1.0
3.2.1.52
false
3.2.1.52
N-acetyl-β-D-glucosamine(anhydrous)-N-acetylmuramate + Water → 1,6-anhydro-N-acetyl-β-muramate + N-Acetyl-D-glucosamine
LEFT_TO_RIGHT
3.5.1.28
false
3.5.1.28
GlcNAc-1,6-anhMurNAc-L-Ala-?-D-Glu-DAP-D-Ala + Water → L-Ala-γ-D-Glu-DAP-D-Ala + N-acetyl-β-D-glucosamine(anhydrous)-N-acetylmuramate
LEFT_TO_RIGHT
1.0
C10H16N5O13P3
Adenosine triphosphate
506.99576
1.0
445675
PubChem-compound
UDP-N-ACETYL-D-GLUCOSAMINE
BioCyc
SMILES
CC(=O)N[C@H]1C(O)O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O
6866-69-9
CAS
CHEBI:16761
ChEBI
B7UYS5
UniProt
CHEBI:506227
ChEBI
SMILES
C[C@@H](O)C(O)=O
1.0
HMDB0000042
HMDB
45479497
PubChem-compound
HMDB0000285
HMDB
SMP0122240
SMPDB
962
PubChem-compound
CHEBI:15366
ChEBI
389248
ChemSpider
SMILES
[H][C@](C)(O[C@@]1([H])[C@]([H])(O[C@]2([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]2([H])N=C(C)[O-])[C@@]2([H])COC([H])(O2)[C@]1([H])N=C(C)O)C(O)=O
CPD0-881
BioCyc
C11H16NO7
1,6-anhydro-N-acetyl-β-muramate
274.09268
5800
ChemSpider
392413
ChemSpider
C37H57N7O20
GlcNAc-1,6-anhMurNAc-L-Ala-?-D-Glu-DAP-D-Ala
919.36694
C00075
KEGG Compound
1.0
PW123548
PathWhiz
Beta-hexosaminidase
C00080
KEGG Compound
1.0
Periplasmic Space
9965052
PubChem-compound
2.0
HMDB0000290
HMDB
Pseudomonas aeruginosa
171
ChemSpider
HMDB0002111
HMDB
CHEBI:42111
ChEBI
CHEBI:15377
ChEBI
CHEBI:15378
ChEBI
SMILES
[H+]
58-64-0
CAS
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
25202885
PubChem-compound
1.0
GlcNAc-1,6-anhMurNAc-L-Ala-?-D-Glu-DAP-D-Ala
1.0
Bifunctional protein GlmU
Phosphoglucosamine mutase
SMILES
N[C@H]1C(O)O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O
61503
PubChem-compound
L-Ala-γ-D-Glu-DAP-D-Ala
444493
PubChem-compound
SMILES
[H]C(C)(O[C@@]1([H])[C@]([H])(O)[C@@]([H])(C[O+]P(O)(O)=O)OC([H])(O)[C@]1([H])[NH+]=C(C)[O-])C([O-])=O
A6UZG7
UniProt
SMILES
N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OP(O)(O)=O
SMILES
CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=O
ACETYL-COA
BioCyc
H2O
Water
18.010565
GlcNAc-1,6-anhMurNAc-L-Ala-?-D-Glu-DAP-D-Ala
SMILES
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP(O)(=O)OP(O)(=O)OP(O)(O)=O)N1C=CC(=O)NC1=O
287
TAXONOMY
63-39-8
CAS
Transport1024
false
GlcNAc-1,6-anhMurNAc-L-Ala-?-D-Glu-DAP-D-Ala (→), Hydrogen Ion (→) Transport: Pseudomonas aeruginosa, Periplasmic Space to Pseudomonas aeruginosa, Cell, Cytosol
LEFT_TO_RIGHT
45479219
PubChem-compound
HMDB0059597
HMDB
Hydrogen Ion
CHEBI:15351
ChEBI
102029-88-9
CAS
176
PubChem-compound
SMILES
CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1OP(O)(O)=O
1.0
85-61-0
CAS
N-Acetylneuraminate, N-Acetylmannosamine, and N-Acetylglucosamine Degradation
SubPathway
7512-17-6
CAS