Cloned (Comment) | Organism |
---|---|
MurC, overexpression in Escherichia coli strain JM83 | Escherichia coli |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
1H-indazole-3-carbohydrazide | - |
Escherichia coli | |
2-(4-{[(E)-2-(1H-indazol-3-ylcarbonyl)hydrazono]methyl} phenoxy) acetic acid | complete inhibition at 0.5 mM | Escherichia coli | |
2-phenyl-1,3-thiazole-5-carbohydrazide | - |
Escherichia coli | |
2-phenyl-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]-1,3-thiazole-5-carbohydrazide | 18% inhibition at 0.25 mM | Escherichia coli | |
2-[4-({(E)-2-[(4-methyl-1,3-thiazol-5-yl)carbonyl]hydrazono} methyl)phenoxy]acetic acid | complete inhibition at 0.5 mM | Escherichia coli | |
4-({(E)-2-[(4-methyl-1,3-thiazol-5-yl)carbonyl]hydrazono} methyl)benzoic acid | 94% inhibition at 0.5 mM | Escherichia coli | |
4-methyl-1,3-thiazole-5-carbohydrazide | - |
Escherichia coli | |
4-methyl-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]-1,3-thiazole-5-carbohydrazide | 26% inhibition at 0.5 mM | Escherichia coli | |
4-methyl-N'-[(E)-(2-phenyl-1,3-thiazol-4-yl)methylidene]-1,3-thiazole-5-carbohydrazide | complete inhibition at 0.5 mM | Escherichia coli | |
4-{[(E)-2-(1H-indazol-3-ylcarbonyl)hydrazono]methyl}benzoic acid | complete inhibition at 0.5 mM | Escherichia coli | |
benzohydrazide | - |
Escherichia coli | |
methyl4-({(E)-2-[(4-methyl-1,3-thiazol-5-yl)carbonyl]hydrazono}methyl)benzoate | 95% inhibition at 0.5 mM | Escherichia coli | |
methyl4-{[(E)-2-(1H-indazol-3-ylcarbonyl)hydrazono]methyl} benzoate | complete inhibition at 0.5 mM | Escherichia coli | |
additional information | inhibitor design and synthesis, mass spectrometric analysis, ligand molecular docking calculations, inhibitory potency, MIC values lay above 0.128 mg/ml, overview | Escherichia coli | |
N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]-1H-indazole-3-carbohydrazide | 42% inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzohydrazide | 64% inhibition at 0.10 mM | Escherichia coli | |
N'-[(E)-(2,4-dihydroxyphenyl)methylidene]-1H-indazole-3-carbohydrazide | 74% inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(2-hydroxyphenyl)methylidene]-1H-indazole-3-carbohydrazide | complete inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(2-phenyl-1,3-thiazol-4-yl)methylidene]-1H-indazole-3-carbohydrazide | 78% inhibition at 0.10 mM | Escherichia coli | |
N'-[(E)-(2-phenyl-1,3-thiazol-4-yl)methylidene]benzohydrazide | 70% inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-1H-indazole-3-carbohydrazide | 36% inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-1,3-thiazole-5-carbohydrazide | 95% inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]benzohydrazide | complete inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-(3,4-dimethoxyphenyl)methylidene]-1H-indazole-3-carbohydrazide | complete inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-(3,4-dimethoxyphenyl)methylidene]-4-methyl-1,3-thiazole-5-carbohydrazide | complete inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-(3,4-dimethoxyphenyl)methylidene]benzohydrazide | 97% inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-(3,5-dichloro-2-hydroxyphenyl)methylidene]-4-methyl-1,3-thiazole-5-carbohydrazide | 43% inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(3-hydroxy-4-methoxyphenyl)methylidene] benzohydrazide | 92% inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-(3-hydroxy-4-methoxyphenyl)methylidene]-1H-indazole-3-carbohydrazide | 67% inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(4-cyanophenyl)methylidene]-1H-indazole-3-carbohydrazide | complete inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(4-cyanophenyl)methylidene]benzohydrazide | complete inhibition at 0.25 mM | Escherichia coli | |
N'-[(E)-(4-nitrophenyl)methylidene]-1H-indazole-3-carbohydrazide | 91% inhibition at 0.5 mM | Escherichia coli | |
N'-[(E)-1H-indol-3-ylmethylidene]-1H-indazole-3-carbohydrazide | complete inhibition at 010 mM | Escherichia coli | |
N'-[(E)-1H-indol-3-ylmethylidene]benzohydrazide | 93% inhibition at 0.5 mM | Escherichia coli | |
N'-{(E)-[4-(dimethylamino)phenyl]methylidene}-1H-indazole-3-carbohydrazide | 95% inhibition at 0.25 mM | Escherichia coli | |
N'-{(E)-[4-(dimethylamino)phenyl]methylidene}-4-methyl-1,3-thiazole-5-carbohydrazide | 97% inhibition at 0.25 mM | Escherichia coli | |
N'-{(E)-[4-(dimethylamino)phenyl]methylidene}benzohydrazide | complete inhibition at 0.25 mM | Escherichia coli | |
N-[(E)-(2,4-dihydroxyphenyl)methylidene]benzohydrazide | complete inhibition at 0.5 mM | Escherichia coli |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Mg2+ | - |
Escherichia coli |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
ATP + UDP-N-acetylmuramate + L-alanine | Escherichia coli | - |
ADP + phosphate + UDP-N-acetylmuramoyl-L-alanine | - |
? | |
additional information | Escherichia coli | the Mur ligases constitute a series of four ATP-dependent enzymes, MurC to Mur, that are responsible for the stepwise addition of the pentapeptide side chain onto the D-lactoyl group of the uridine diphosphate-N-acetylmuramic acid initially formed via MurA and MurB, MurC catalyzes the additon of the first amino acid L-alanine. All of the Mur ligases catalyze the formation of an amide or peptide bond through the same reaction mechanism via a tetrahedral intermediate, overview | ? | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Escherichia coli | - |
- |
- |
Purification (Comment) | Organism |
---|---|
recombinant MurC from Escherichia coli strain JM83 by anion exchange chromatography | Escherichia coli |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
ATP + UDP-N-acetylmuramate + L-alanine | - |
Escherichia coli | ADP + phosphate + UDP-N-acetylmuramoyl-L-alanine | - |
? | |
additional information | the Mur ligases constitute a series of four ATP-dependent enzymes, MurC to Mur, that are responsible for the stepwise addition of the pentapeptide side chain onto the D-lactoyl group of the uridine diphosphate-N-acetylmuramic acid initially formed via MurA and MurB, MurC catalyzes the additon of the first amino acid L-alanine. All of the Mur ligases catalyze the formation of an amide or peptide bond through the same reaction mechanism via a tetrahedral intermediate, overview | Escherichia coli | ? | - |
? |
Synonyms | Comment | Organism |
---|---|---|
MurC | - |
Escherichia coli |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
37 | - |
assay at | Escherichia coli |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
8 | - |
malachite green assay at | Escherichia coli |
8.6 | - |
radioactive assay at | Escherichia coli |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
ATP | - |
Escherichia coli |
IC50 Value | IC50 Value Maximum | Comment | Organism | Inhibitor | Structure |
---|---|---|---|---|---|
0.032 | - |
pH 8.0, 37°C | Escherichia coli | 2-phenyl-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]-1,3-thiazole-5-carbohydrazide | |
0.123 | - |
pH 8.0, 37°C | Escherichia coli | 1H-indazole-3-carbohydrazide |