Inhibitors | Comment | Organism | Structure |
---|---|---|---|
2',3'-O-[4-(dihydroxyiminio)-2,6-dinitrocyclohexa-2,5-diene-1,1-diyl]guanosine 5'-triphosphate | - |
Caulobacter vibrioides | |
2',3'-O-[4-(dihydroxyiminio)-2,6-dinitrocyclohexa-2,5-diene-1,1-diyl]guanosine 5'-triphosphate | - |
Clostridioides difficile | |
2',3'-O-[4-(dihydroxyiminio)-2,6-dinitrocyclohexa-2,5-diene-1,1-diyl]guanosine 5'-triphosphate | - |
Komagataeibacter xylinus | |
2',3'-O-[4-(dihydroxyiminio)-2,6-dinitrocyclohexa-2,5-diene-1,1-diyl]guanosine 5'-triphosphate | - |
Pseudomonas aeruginosa | |
2',3'-O-[4-(dihydroxyiminio)-2,6-dinitrocyclohexa-2,5-diene-1,1-diyl]guanosine 5'-triphosphate | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
2',3'-O-[4-(dihydroxyiminio)-2,6-dinitrocyclohexa-2,5-diene-1,1-diyl]guanosine 5'-triphosphate | - |
Synechocystis sp. PCC 6803 | |
2',3'-O-[4-(dihydroxyiminio)-2,6-dinitrocyclohexa-2,5-diene-1,1-diyl]guanosine 5'-triphosphate | - |
Vibrio cholerae serotype O1 | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-(gammaS)triphosphate | - |
Caulobacter vibrioides | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-(gammaS)triphosphate | - |
Clostridioides difficile | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-(gammaS)triphosphate | - |
Komagataeibacter xylinus | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-(gammaS)triphosphate | - |
Pseudomonas aeruginosa | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-(gammaS)triphosphate | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-(gammaS)triphosphate | - |
Synechocystis sp. PCC 6803 | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-(gammaS)triphosphate | - |
Vibrio cholerae serotype O1 | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-triphosphate | - |
Caulobacter vibrioides | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-triphosphate | - |
Clostridioides difficile | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-triphosphate | - |
Komagataeibacter xylinus | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-triphosphate | - |
Pseudomonas aeruginosa | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-triphosphate | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-triphosphate | - |
Synechocystis sp. PCC 6803 | |
2'-O-[2-(methylamino)benzoyl]guanosine 5'-triphosphate | - |
Vibrio cholerae serotype O1 | |
2-hydroxy-5-[(E)-[4-[(pyridin-2-yl)sulfamoyl]phenyl]diazenyl]benzoic acid | - |
Caulobacter vibrioides | |
2-hydroxy-5-[(E)-[4-[(pyridin-2-yl)sulfamoyl]phenyl]diazenyl]benzoic acid | - |
Clostridioides difficile | |
2-hydroxy-5-[(E)-[4-[(pyridin-2-yl)sulfamoyl]phenyl]diazenyl]benzoic acid | - |
Komagataeibacter xylinus | |
2-hydroxy-5-[(E)-[4-[(pyridin-2-yl)sulfamoyl]phenyl]diazenyl]benzoic acid | - |
Pseudomonas aeruginosa | |
2-hydroxy-5-[(E)-[4-[(pyridin-2-yl)sulfamoyl]phenyl]diazenyl]benzoic acid | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
2-hydroxy-5-[(E)-[4-[(pyridin-2-yl)sulfamoyl]phenyl]diazenyl]benzoic acid | - |
Synechocystis sp. PCC 6803 | |
2-hydroxy-5-[(E)-[4-[(pyridin-2-yl)sulfamoyl]phenyl]diazenyl]benzoic acid | - |
Vibrio cholerae serotype O1 | |
3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucuronopyranosyl soyasapogenol B 22-O-alpha-D-glucopyranoside | - |
Caulobacter vibrioides | |
3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucuronopyranosyl soyasapogenol B 22-O-alpha-D-glucopyranoside | - |
Clostridioides difficile | |
3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucuronopyranosyl soyasapogenol B 22-O-alpha-D-glucopyranoside | - |
Komagataeibacter xylinus | |
3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucuronopyranosyl soyasapogenol B 22-O-alpha-D-glucopyranoside | - |
Pseudomonas aeruginosa | |
3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucuronopyranosyl soyasapogenol B 22-O-alpha-D-glucopyranoside | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucuronopyranosyl soyasapogenol B 22-O-alpha-D-glucopyranoside | - |
Synechocystis sp. PCC 6803 | |
3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucuronopyranosyl soyasapogenol B 22-O-alpha-D-glucopyranoside | - |
Vibrio cholerae serotype O1 | |
3-O-alpha-L-rhamnopyronosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-gluconopyranosyl soyasapogenol B 22-o-alpha-D-glucopyranoside | potent non-competitive inhibitor in vitro, not membrane-permeable | Komagataeibacter xylinus | |
4-(2,5-dimethylphenoxy)-N-(4-morpholin-4-ylphenyl)butanamide | - |
Caulobacter vibrioides | |
4-(2,5-dimethylphenoxy)-N-(4-morpholin-4-ylphenyl)butanamide | - |
Clostridioides difficile | |
4-(2,5-dimethylphenoxy)-N-(4-morpholin-4-ylphenyl)butanamide | - |
Komagataeibacter xylinus | |
4-(2,5-dimethylphenoxy)-N-(4-morpholin-4-ylphenyl)butanamide | - |
Pseudomonas aeruginosa | |
4-(2,5-dimethylphenoxy)-N-(4-morpholin-4-ylphenyl)butanamide | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
4-(2,5-dimethylphenoxy)-N-(4-morpholin-4-ylphenyl)butanamide | - |
Synechocystis sp. PCC 6803 | |
4-(2,5-dimethylphenoxy)-N-(4-morpholin-4-ylphenyl)butanamide | - |
Vibrio cholerae serotype O1 | |
4-chloro-3-nitro-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzene-1-sulfonohydrazide | - |
Caulobacter vibrioides | |
4-chloro-3-nitro-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzene-1-sulfonohydrazide | - |
Clostridioides difficile | |
4-chloro-3-nitro-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzene-1-sulfonohydrazide | - |
Komagataeibacter xylinus | |
4-chloro-3-nitro-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzene-1-sulfonohydrazide | - |
Pseudomonas aeruginosa | |
4-chloro-3-nitro-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzene-1-sulfonohydrazide | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
4-chloro-3-nitro-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzene-1-sulfonohydrazide | - |
Synechocystis sp. PCC 6803 | |
4-chloro-3-nitro-N'-[(E)-(2,3,4-trihydroxyphenyl)methylidene]benzene-1-sulfonohydrazide | - |
Vibrio cholerae serotype O1 | |
9-(3-[4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]-1H-1,2,3-triazol-1-yl]propyl)-6-chloro-9H-purin-2-amine | - |
Caulobacter vibrioides | |
9-(3-[4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]-1H-1,2,3-triazol-1-yl]propyl)-6-chloro-9H-purin-2-amine | - |
Clostridioides difficile | |
9-(3-[4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]-1H-1,2,3-triazol-1-yl]propyl)-6-chloro-9H-purin-2-amine | - |
Komagataeibacter xylinus | |
9-(3-[4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]-1H-1,2,3-triazol-1-yl]propyl)-6-chloro-9H-purin-2-amine | - |
Pseudomonas aeruginosa | |
9-(3-[4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]-1H-1,2,3-triazol-1-yl]propyl)-6-chloro-9H-purin-2-amine | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
9-(3-[4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]-1H-1,2,3-triazol-1-yl]propyl)-6-chloro-9H-purin-2-amine | - |
Synechocystis sp. PCC 6803 | |
9-(3-[4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]-1H-1,2,3-triazol-1-yl]propyl)-6-chloro-9H-purin-2-amine | - |
Vibrio cholerae serotype O1 | |
cyclic di-3',5'-(2'-fluoroguanylate) | - |
Caulobacter vibrioides | |
cyclic di-3',5'-(2'-fluoroguanylate) | - |
Clostridioides difficile | |
cyclic di-3',5'-(2'-fluoroguanylate) | - |
Komagataeibacter xylinus | |
cyclic di-3',5'-(2'-fluoroguanylate) | - |
Pseudomonas aeruginosa | |
cyclic di-3',5'-(2'-fluoroguanylate) | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
cyclic di-3',5'-(2'-fluoroguanylate) | - |
Synechocystis sp. PCC 6803 | |
cyclic di-3',5'-(2'-fluoroguanylate) | - |
Vibrio cholerae serotype O1 | |
cyclic di-3',5'-inosinylic acid | - |
Caulobacter vibrioides | |
cyclic di-3',5'-inosinylic acid | - |
Clostridioides difficile | |
cyclic di-3',5'-inosinylic acid | - |
Komagataeibacter xylinus | |
cyclic di-3',5'-inosinylic acid | - |
Pseudomonas aeruginosa | |
cyclic di-3',5'-inosinylic acid | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
cyclic di-3',5'-inosinylic acid | - |
Synechocystis sp. PCC 6803 | |
cyclic di-3',5'-inosinylic acid | - |
Vibrio cholerae serotype O1 | |
cyclo-di-GMP | - |
Synechocystis sp. PCC 6803 | |
cyclo-di-inosinylic acid | - |
Synechocystis sp. PCC 6803 | |
ebselen | - |
Caulobacter vibrioides | |
ebselen | - |
Clostridioides difficile | |
ebselen | - |
Komagataeibacter xylinus | |
ebselen | - |
Pseudomonas aeruginosa | |
ebselen | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
ebselen | - |
Synechocystis sp. PCC 6803 | |
ebselen | - |
Vibrio cholerae serotype O1 | |
eprosartan | - |
Caulobacter vibrioides | |
eprosartan | - |
Clostridioides difficile | |
eprosartan | - |
Komagataeibacter xylinus | |
eprosartan | - |
Pseudomonas aeruginosa | |
eprosartan | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
eprosartan | - |
Synechocystis sp. PCC 6803 | |
eprosartan | - |
Vibrio cholerae serotype O1 | |
additional information | screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2' (3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases; screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2' (3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases | Caulobacter vibrioides | |
additional information | screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2' (3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases | Clostridioides difficile | |
additional information | screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2'(3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases | Komagataeibacter xylinus | |
additional information | screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2' (3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases; screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2'(3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases | Pseudomonas aeruginosa | |
additional information | screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2' (3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases | Salmonella enterica subsp. enterica serovar Typhimurium | |
additional information | screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2'(3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases | Synechocystis sp. PCC 6803 | |
additional information | screenings for chemicals capable of inhibiting the c-di-GMP synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation. 2',3'-O-(2,4,6-trinitrophenyl) (TNP)- and 2' (3')-O-(N-methylanthraniloyl) (MANT)-substituted nucleotides are potent inhibitors of guanylyl and adenylyl cyclases | Vibrio cholerae serotype O1 | |
N'-((1E)-(4-ethoxy-3-[(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)methylphenyl)methylene)]-3,4,5-trihydroxybenzohydrazide | LP3134; LP3134 | Caulobacter vibrioides | |
N'-((1E)-(4-ethoxy-3-[(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)methylphenyl)methylene)]-3,4,5-trihydroxybenzohydrazide | LP3134 | Clostridioides difficile | |
N'-((1E)-(4-ethoxy-3-[(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)methylphenyl)methylene)]-3,4,5-trihydroxybenzohydrazide | LP3134 | Komagataeibacter xylinus | |
N'-((1E)-(4-ethoxy-3-[(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)methylphenyl)methylene)]-3,4,5-trihydroxybenzohydrazide | LP3134; LP3134 | Pseudomonas aeruginosa | |
N'-((1E)-(4-ethoxy-3-[(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)methylphenyl)methylene)]-3,4,5-trihydroxybenzohydrazide | LP3134 | Salmonella enterica subsp. enterica serovar Typhimurium | |
N'-((1E)-(4-ethoxy-3-[(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)methylphenyl)methylene)]-3,4,5-trihydroxybenzohydrazide | LP3134 | Synechocystis sp. PCC 6803 | |
N'-((1E)-(4-ethoxy-3-[(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)methylphenyl)methylene)]-3,4,5-trihydroxybenzohydrazide | LP3134 | Vibrio cholerae serotype O1 | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-3-nitrobenzene-1-sulfonohydrazide | - |
Caulobacter vibrioides | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-3-nitrobenzene-1-sulfonohydrazide | - |
Clostridioides difficile | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-3-nitrobenzene-1-sulfonohydrazide | - |
Komagataeibacter xylinus | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-3-nitrobenzene-1-sulfonohydrazide | - |
Pseudomonas aeruginosa | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-3-nitrobenzene-1-sulfonohydrazide | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-3-nitrobenzene-1-sulfonohydrazide | - |
Synechocystis sp. PCC 6803 | |
N'-[(E)-(3,4-dihydroxyphenyl)methylidene]-4-methyl-3-nitrobenzene-1-sulfonohydrazide | - |
Vibrio cholerae serotype O1 | |
N-(4-anilinophenyl)benzamide | - |
Caulobacter vibrioides | |
N-(4-anilinophenyl)benzamide | - |
Clostridioides difficile | |
N-(4-anilinophenyl)benzamide | - |
Komagataeibacter xylinus | |
N-(4-anilinophenyl)benzamide | - |
Pseudomonas aeruginosa | |
N-(4-anilinophenyl)benzamide | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
N-(4-anilinophenyl)benzamide | - |
Synechocystis sp. PCC 6803 | |
N-(4-anilinophenyl)benzamide | - |
Vibrio cholerae serotype O1 | |
[2- oxo-2-(2-oxopyrrolidin-1-yl)ethyl] 1,3-benzothiazole-6-carboxylate | - |
Caulobacter vibrioides | |
[2- oxo-2-(2-oxopyrrolidin-1-yl)ethyl] 1,3-benzothiazole-6-carboxylate | - |
Clostridioides difficile | |
[2- oxo-2-(2-oxopyrrolidin-1-yl)ethyl] 1,3-benzothiazole-6-carboxylate | - |
Komagataeibacter xylinus | |
[2- oxo-2-(2-oxopyrrolidin-1-yl)ethyl] 1,3-benzothiazole-6-carboxylate | - |
Pseudomonas aeruginosa | |
[2- oxo-2-(2-oxopyrrolidin-1-yl)ethyl] 1,3-benzothiazole-6-carboxylate | - |
Salmonella enterica subsp. enterica serovar Typhimurium | |
[2- oxo-2-(2-oxopyrrolidin-1-yl)ethyl] 1,3-benzothiazole-6-carboxylate | - |
Synechocystis sp. PCC 6803 | |
[2- oxo-2-(2-oxopyrrolidin-1-yl)ethyl] 1,3-benzothiazole-6-carboxylate | - |
Vibrio cholerae serotype O1 |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
2 GTP | Pseudomonas aeruginosa | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Caulobacter vibrioides | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Komagataeibacter xylinus | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Synechocystis sp. PCC 6803 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Clostridioides difficile | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Salmonella enterica subsp. enterica serovar Typhimurium | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Vibrio cholerae serotype O1 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Caulobacter vibrioides CB15N | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Pseudomonas aeruginosa ATCC 15692 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Salmonella enterica subsp. enterica serovar Typhimurium SGSC1412 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Caulobacter vibrioides NA1000 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Pseudomonas aeruginosa 1C | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Salmonella enterica subsp. enterica serovar Typhimurium ATCC 700720 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Pseudomonas aeruginosa PRS 101 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Pseudomonas aeruginosa DSM 22644 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Pseudomonas aeruginosa CIP 104116 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Pseudomonas aeruginosa LMG 12228 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Vibrio cholerae serotype O1 El Tor Inaba N16961 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Pseudomonas aeruginosa JCM 14847 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | Vibrio cholerae serotype O1 ATCC 39315 | - |
2 diphosphate + cyclic di-3',5'-guanylate | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Caulobacter vibrioides | A0A0H3CCZ8 | Caulobacter crescentus | - |
Caulobacter vibrioides | B8GZM2 | - |
- |
Caulobacter vibrioides CB15N | A0A0H3CCZ8 | Caulobacter crescentus | - |
Caulobacter vibrioides NA1000 | A0A0H3CCZ8 | Caulobacter crescentus | - |
Caulobacter vibrioides NA1000 | B8GZM2 | - |
- |
Clostridioides difficile | A0A170Y3L9 | Peptoclostridium difficile or Clostridium difficile | - |
Komagataeibacter xylinus | O87374 | Gluconoacetobacter xylinus or Acetobacter xylinum | - |
Pseudomonas aeruginosa | Q9HT84 | - |
- |
Pseudomonas aeruginosa | Q9HXT9 | - |
- |
Pseudomonas aeruginosa 1C | Q9HT84 | - |
- |
Pseudomonas aeruginosa 1C | Q9HXT9 | - |
- |
Pseudomonas aeruginosa ATCC 15692 | Q9HT84 | - |
- |
Pseudomonas aeruginosa ATCC 15692 | Q9HXT9 | - |
- |
Pseudomonas aeruginosa CIP 104116 | Q9HT84 | - |
- |
Pseudomonas aeruginosa CIP 104116 | Q9HXT9 | - |
- |
Pseudomonas aeruginosa DSM 22644 | Q9HT84 | - |
- |
Pseudomonas aeruginosa DSM 22644 | Q9HXT9 | - |
- |
Pseudomonas aeruginosa JCM 14847 | Q9HT84 | - |
- |
Pseudomonas aeruginosa JCM 14847 | Q9HXT9 | - |
- |
Pseudomonas aeruginosa LMG 12228 | Q9HT84 | - |
- |
Pseudomonas aeruginosa LMG 12228 | Q9HXT9 | - |
- |
Pseudomonas aeruginosa PRS 101 | Q9HT84 | - |
- |
Pseudomonas aeruginosa PRS 101 | Q9HXT9 | - |
- |
Salmonella enterica subsp. enterica serovar Typhimurium | Q8ZNT5 | - |
- |
Salmonella enterica subsp. enterica serovar Typhimurium ATCC 700720 | Q8ZNT5 | - |
- |
Salmonella enterica subsp. enterica serovar Typhimurium SGSC1412 | Q8ZNT5 | - |
- |
Synechocystis sp. PCC 6803 | P73272 | - |
- |
Vibrio cholerae serotype O1 | Q9KKZ4 | - |
- |
Vibrio cholerae serotype O1 ATCC 39315 | Q9KKZ4 | - |
- |
Vibrio cholerae serotype O1 El Tor Inaba N16961 | Q9KKZ4 | - |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
2 GTP | - |
Pseudomonas aeruginosa | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Caulobacter vibrioides | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Komagataeibacter xylinus | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Synechocystis sp. PCC 6803 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Clostridioides difficile | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Salmonella enterica subsp. enterica serovar Typhimurium | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Vibrio cholerae serotype O1 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The DgcP of Caulobacter crescentus binds dimeric c-di-GMP at an allosteric site I-site that is characterized by the RxxD motif. Binding of cyclic-di-GMP at the I-site accounts for a strong non-competitive product inhibition, which establishes a limit on the cellular c-di-GMP concentration | Caulobacter vibrioides | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Komagataeibacter xylinus | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Synechocystis sp. PCC 6803 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Clostridioides difficile | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Salmonella enterica subsp. enterica serovar Typhimurium | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Vibrio cholerae serotype O1 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Caulobacter vibrioides CB15N | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Pseudomonas aeruginosa ATCC 15692 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa ATCC 15692 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Salmonella enterica subsp. enterica serovar Typhimurium SGSC1412 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Salmonella enterica subsp. enterica serovar Typhimurium SGSC1412 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Caulobacter vibrioides NA1000 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The DgcP of Caulobacter crescentus binds dimeric c-di-GMP at an allosteric site I-site that is characterized by the RxxD motif. Binding of cyclic-di-GMP at the I-site accounts for a strong non-competitive product inhibition, which establishes a limit on the cellular c-di-GMP concentration | Caulobacter vibrioides NA1000 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Pseudomonas aeruginosa 1C | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa 1C | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Salmonella enterica subsp. enterica serovar Typhimurium ATCC 700720 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Salmonella enterica subsp. enterica serovar Typhimurium ATCC 700720 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Pseudomonas aeruginosa PRS 101 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa PRS 101 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Pseudomonas aeruginosa DSM 22644 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa DSM 22644 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Pseudomonas aeruginosa CIP 104116 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa CIP 104116 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Pseudomonas aeruginosa LMG 12228 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa LMG 12228 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Vibrio cholerae serotype O1 El Tor Inaba N16961 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Vibrio cholerae serotype O1 El Tor Inaba N16961 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Pseudomonas aeruginosa JCM 14847 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Pseudomonas aeruginosa JCM 14847 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | - |
Vibrio cholerae serotype O1 ATCC 39315 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? | |
2 GTP | the enzyme uses its GGDEF domain for catalysis. The GGDEF signature domain forms part of the active site A-site where GTP is bound (one molecule of GTP substrate per monomer) | Vibrio cholerae serotype O1 ATCC 39315 | 2 diphosphate + cyclic di-3',5'-guanylate | - |
? |
Synonyms | Comment | Organism |
---|---|---|
DGC | - |
Pseudomonas aeruginosa |
DGC | - |
Caulobacter vibrioides |
DGC | - |
Komagataeibacter xylinus |
DGC | - |
Synechocystis sp. PCC 6803 |
DGC | - |
Clostridioides difficile |
DGC | - |
Salmonella enterica subsp. enterica serovar Typhimurium |
DGC | - |
Vibrio cholerae serotype O1 |
Dgc1 | - |
Komagataeibacter xylinus |
DgcA | - |
Caulobacter vibrioides |
DgcP | - |
Pseudomonas aeruginosa |
PleD | - |
Caulobacter vibrioides |
Slr1143 | - |
Synechocystis sp. PCC 6803 |
WspR | - |
Pseudomonas aeruginosa |
IC50 Value | IC50 Value Maximum | Comment | Organism | Inhibitor | Structure |
---|---|---|---|---|---|
0.005 | - |
pH and temperature not specified in the publication | Komagataeibacter xylinus | 3-O-alpha-L-rhamnopyronosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-gluconopyranosyl soyasapogenol B 22-o-alpha-D-glucopyranoside | |
0.011 | - |
pH and temperature not specified in the publication | Pseudomonas aeruginosa | cyclic di-3',5'-(2'-fluoroguanylate) | |
0.1 | - |
about, pH and temperature not specified in the publication | Synechocystis sp. PCC 6803 | cyclic di-3',5'-(2'-fluoroguanylate) |
General Information | Comment | Organism |
---|---|---|
malfunction | enzyme inhibition by inhibitors causes inhibition of biofilm formation of the organism | Pseudomonas aeruginosa |
malfunction | enzyme inhibition by inhibitors causes inhibition of biofilm formation of the organism | Caulobacter vibrioides |
malfunction | enzyme inhibition by inhibitors causes inhibition of biofilm formation of the organism | Komagataeibacter xylinus |
malfunction | enzyme inhibition by inhibitors causes inhibition of biofilm formation of the organism | Synechocystis sp. PCC 6803 |
malfunction | enzyme inhibition by inhibitors causes inhibition of biofilm formation of the organism | Clostridioides difficile |
malfunction | enzyme inhibition by inhibitors causes inhibition of biofilm formation of the organism | Salmonella enterica subsp. enterica serovar Typhimurium |
malfunction | enzyme inhibition by inhibitors causes inhibition of biofilm formation of the organism | Vibrio cholerae serotype O1 |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain | Pseudomonas aeruginosa |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain | Caulobacter vibrioides |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain | Komagataeibacter xylinus |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain | Synechocystis sp. PCC 6803 |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain | Vibrio cholerae serotype O1 |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain. The enzyme is important for the organism's biofilm formation ability, which plays a pivotal role in the virulence | Pseudomonas aeruginosa |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain. The enzyme is important for the organism's biofilm formation ability, which plays a pivotal role in the virulence | Clostridioides difficile |
physiological function | the primary signaling molecule promoting bacterial biofilm formation is the universal second messenger cyclic di-GMP. This dinucleotide predominantly controls the gene expression of motility, adhesins, and capsule production to coordinate biofilm formation. Cyclic di-GMP is synthesized by diguanylate cyclases (DGCs) that have a GGDEF domain and is degraded by phosphodiesterases (PDEs) containing either an EAL or an HD-GYP domain. The enzyme is important for the organism's biofilm formation ability, which plays a pivotal role in the virulence | Salmonella enterica subsp. enterica serovar Typhimurium |