Cloned (Comment) | Organism |
---|---|
gene ugmA, recombinant expression in Escherichia coli strain BL21(DE3) | Mycobacterium tuberculosis |
gene ugmA, recombinant expression in Escherichia coli strain BL21(DE3) | Klebsiella pneumoniae |
gene ugmA, recombinant expression in Escherichia coli strain ER2523 | Corynebacterium diphtheriae |
Inhibitors | Comment | Organism | Structure |
---|---|---|---|
2-((4-(3,4-dichlorophenyl)thiazol-2-yl)amino)-3-(4-iodophenyl)propanoic acid | - |
Caenorhabditis elegans | |
2-((4-(3,4-dichlorophenyl)thiazol-2-yl)amino)-3-(4-iodophenyl)propanoic acid | - |
Corynebacterium diphtheriae | |
2-((4-(3,4-dichlorophenyl)thiazol-2-yl)amino)-3-(4-iodophenyl)propanoic acid | - |
Klebsiella pneumoniae | |
2-((4-(3,4-dichlorophenyl)thiazol-2-yl)amino)-3-(4-iodophenyl)propanoic acid | - |
Mycobacterium tuberculosis | |
2-(3-((4-chlorophenoxy)methyl)-6-(p-tolyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 97% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-((4-chlorophenoxy)methyl)-6-(p-tolyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 97% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-((4-chlorophenoxy)methyl)-6-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 95% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-((4-chlorophenoxy)methyl)-6-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 95% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(2-methylfuran-3-yl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 25% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(2-methylfuran-3-yl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 25% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(4-bromobenzyl)-6-(4-chlorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | - |
Caenorhabditis elegans | |
2-(3-(4-bromobenzyl)-6-(4-chlorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | - |
Corynebacterium diphtheriae | |
2-(3-(4-bromobenzyl)-6-(4-chlorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | second generation compound, competitive, 100% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(4-bromobenzyl)-6-(4-chlorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | second generation compound, competitive, 100% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(4-fluorobenzyl)-6-(p-tolyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 96% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(4-fluorobenzyl)-6-(p-tolyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 96% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(4-fluorobenzyl)-6-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 92% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(4-fluorobenzyl)-6-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 92% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(4-fluorobenzyl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 92% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(4-fluorobenzyl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 92% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(4-fluorophenyl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 74% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(4-fluorophenyl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 74% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(furan-2-yl)-6-(p-tolyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 62% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(furan-2-yl)-6-(p-tolyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 62% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(furan-2-yl)-6-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 46% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(furan-2-yl)-6-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 46% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-(furan-2-yl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 34% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-(furan-2-yl)-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 34% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(3-cyclopropyl-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 8.9% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(3-cyclopropyl-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 8.9% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(6-(4-chlorophenyl)-3-(2-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 91% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(6-(4-chlorophenyl)-3-(2-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 91% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(6-(4-chlorophenyl)-3-(4-fluorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 96% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(6-(4-chlorophenyl)-3-(4-fluorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 96% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(6-(4-chlorophenyl)-3-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | - |
Caenorhabditis elegans | |
2-(6-(4-chlorophenyl)-3-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | - |
Corynebacterium diphtheriae | |
2-(6-(4-chlorophenyl)-3-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | first generation compound, competitive, 95% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(6-(4-chlorophenyl)-3-(thiophen-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | first generation compound, competitive, 95% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(6-(4-chlorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 72% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(6-(4-chlorophenyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 72% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
2-(6-(4-fluorophenyl)-3-(furan-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 38% inhibition at 0.1 mM | Klebsiella pneumoniae | |
2-(6-(4-fluorophenyl)-3-(furan-2-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazin-7-yl)acetic acid | 38% inhibition at 0.1 mM | Mycobacterium tuberculosis | |
3-(3-(2-(allylamino)thiazol-4-yl)-2,5-dimethyl-1H-pyrrol-1-yl)propanoic acid | - |
Klebsiella pneumoniae | |
3-(3-(2-(allylamino)thiazol-4-yl)-2,5-dimethyl-1H-pyrrol-1-yl)propanoic acid | - |
Mycobacterium tuberculosis | |
3-(6-(benzyloxy)-1H-indol-1-yl)propanoic acid | - |
Klebsiella pneumoniae | |
3-(6-(benzyloxy)-1H-indol-1-yl)propanoic acid | - |
Mycobacterium tuberculosis | |
additional information | structure-based virtual screening for UDP-galactopyranose mutase ligands identifies a class of antimycobacterial agents, triazolothiadiazine inhibitors, using structures of UGMs from Aspergillus fumigatus, Trypanosoma cruzi, and Klebsiella pneumoniae (PDB ID 3INT) | Caenorhabditis elegans | |
additional information | structure-based virtual screening for UDP-galactopyranose mutase ligands identifies a class of antimycobacterial agents, triazolothiadiazine inhibitors, using structures of UGMs from Aspergillus fumigatus, Trypanosoma cruzi, and Klebsiella pneumoniae (PDB ID 3INT) | Corynebacterium diphtheriae | |
additional information | structure-based virtual screening for UDP-galactopyranose mutase ligands identifies a class of antimycobacterial agents, triazolothiadiazine inhibitors, using structures of UGMs from Aspergillus fumigatus, Trypanosoma cruzi, and Klebsiella pneumoniae (PDB ID 3INT) | Klebsiella pneumoniae | |
additional information | structure-based virtual screening for UDP-galactopyranose mutase ligands identifies a class of antimycobacterial agents, triazolothiadiazine inhibitors, using structures of UGMs from Aspergillus fumigatus, Trypanosoma cruzi, and Klebsiella pneumoniae (PDB ID 3INT) | Mycobacterium tuberculosis |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
UDP-alpha-D-galactopyranose | Caenorhabditis elegans | - |
UDP-alpha-D-galactofuranose | - |
r | |
UDP-alpha-D-galactopyranose | Mycobacterium tuberculosis | - |
UDP-alpha-D-galactofuranose | - |
r | |
UDP-alpha-D-galactopyranose | Klebsiella pneumoniae | - |
UDP-alpha-D-galactofuranose | - |
r | |
UDP-alpha-D-galactopyranose | Corynebacterium diphtheriae | - |
UDP-alpha-D-galactofuranose | - |
r |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Caenorhabditis elegans | - |
- |
- |
Corynebacterium diphtheriae | Q6NER4 | - |
- |
Klebsiella pneumoniae | Q48485 | - |
- |
Mycobacterium tuberculosis | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
UDP-alpha-D-galactopyranose | - |
Caenorhabditis elegans | UDP-alpha-D-galactofuranose | - |
r | |
UDP-alpha-D-galactopyranose | - |
Mycobacterium tuberculosis | UDP-alpha-D-galactofuranose | - |
r | |
UDP-alpha-D-galactopyranose | - |
Klebsiella pneumoniae | UDP-alpha-D-galactofuranose | - |
r | |
UDP-alpha-D-galactopyranose | - |
Corynebacterium diphtheriae | UDP-alpha-D-galactofuranose | - |
r |
Synonyms | Comment | Organism |
---|---|---|
Glf | - |
Caenorhabditis elegans |
Glf | - |
Mycobacterium tuberculosis |
Glf | - |
Klebsiella pneumoniae |
Glf | - |
Corynebacterium diphtheriae |
UGM | - |
Caenorhabditis elegans |
UGM | - |
Mycobacterium tuberculosis |
UGM | - |
Klebsiella pneumoniae |
UGM | - |
Corynebacterium diphtheriae |
uridine 5'-diphosphate-galactopyranose mutase | - |
Caenorhabditis elegans |
uridine 5'-diphosphate-galactopyranose mutase | - |
Mycobacterium tuberculosis |
uridine 5'-diphosphate-galactopyranose mutase | - |
Klebsiella pneumoniae |
uridine 5'-diphosphate-galactopyranose mutase | - |
Corynebacterium diphtheriae |
Cofactor | Comment | Organism | Structure |
---|---|---|---|
FAD | enzyme UGM possesses a flavin adenine dinucleotide (FAD) cofactor that it uses to catalyze ring contraction of UDP-galactopyranose (UDP-Galp) to form UDP-galactofuranose (UDP-Galf) | Caenorhabditis elegans | |
FAD | enzyme UGM possesses a flavin adenine dinucleotide (FAD) cofactor that it uses to catalyze ring contraction of UDP-galactopyranose (UDP-Galp) to form UDP-galactofuranose (UDP-Galf) | Mycobacterium tuberculosis | |
FAD | enzyme UGM possesses a flavin adenine dinucleotide (FAD) cofactor that it uses to catalyze ring contraction of UDP-galactopyranose (UDP-Galp) to form UDP-galactofuranose (UDP-Galf) | Klebsiella pneumoniae | |
FAD | enzyme UGM possesses a flavin adenine dinucleotide (FAD) cofactor that it uses to catalyze ring contraction of UDP-galactopyranose (UDP-Galp) to form UDP-galactofuranose (UDP-Galf) | Corynebacterium diphtheriae |
General Information | Comment | Organism |
---|---|---|
evolution | all organisms that generate Galf-containing glycans encode a UGM homologue | Caenorhabditis elegans |
evolution | all organisms that generate Galf-containing glycans encode a UGM homologue | Mycobacterium tuberculosis |
evolution | all organisms that generate Galf-containing glycans encode a UGM homologue | Klebsiella pneumoniae |
evolution | all organisms that generate Galf-containing glycans encode a UGM homologue | Corynebacterium diphtheriae |
physiological function | the enzyme catalyzes the formation of UDP-galactofuranose (UDP-Galf), which is required to produce Galf-containing glycoconjugates | Caenorhabditis elegans |
physiological function | the enzyme catalyzes the formation of UDP-galactofuranose (UDP-Galf), which is required to produce Galf-containing glycoconjugates | Mycobacterium tuberculosis |
physiological function | the enzyme catalyzes the formation of UDP-galactofuranose (UDP-Galf), which is required to produce Galf-containing glycoconjugates | Klebsiella pneumoniae |
physiological function | the enzyme catalyzes the formation of UDP-galactofuranose (UDP-Galf), which is required to produce Galf-containing glycoconjugates | Corynebacterium diphtheriae |