Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
UDP-glucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
UDP-glucose + [(1-3)-beta-D-glucosyl]n
UDP + [(1-3)-beta-D-glucosyl]n+1
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
additional information
?
-
UDP-glucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDP-glucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDP-glucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDP-glucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1-3)-beta-D-glucosyl]n
UDP + [(1-3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1-3)-beta-D-glucosyl]n
UDP + [(1-3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
specific for UDPglucose as glucosyl donor
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
synthesis of callose in higher plants, enzyme is latent in intact and undamaged cells, it is activated only under perturbed conditions, possible involvement in wound-healing process and in defense against pathogens, enzyme seems to play a vital role in a number of specialized developmental processes in plants, namely pollen maturation and sieve pore formation and gravitropism
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
chain length 60-80
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
production of cell wall polysaccharide found in yeast cells
chain length 60-80
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
additional information
?
-
-
main biosynthetic enzyme responsible for the callose response to biotic, abiotic, and chemical stresses, but not for callose deposition that is part of normal cell development. Enzyme negatively regulates salicylic acid defense signaling pathway
-
-
?
additional information
?
-
-
cell wall biosynthetic enzyme
-
-
?
additional information
?
-
-
1,3-beta-D-glucan synthase catalyses the synthesis of 1,3-beta-D-glucan, the most abundant component of the fungal cell wall.
-
-
?
additional information
?
-
-
the recombinant cytoplasmic domain binds specifically to UDP-agarose and lichenan (beta-glucan), but not to ADP-agarose, GDP-agarose, or other carbohydrates
-
-
?
additional information
?
-
-
cell wall biosynthetic enzyme
-
-
?
additional information
?
-
-
simple and sensitive method for characterization of enzyme products by analysis of newly synthesized polysaccharides by 13C-nuclear magnetic resonance
-
-
?
additional information
?
-
the purified yeast glucan synthase produces glucan with a length of 6550 plus/minus 760 mer. Pre-steady state kinetics analysis reveal a highly efficient but rate-determining chain elongation rate of 51.5 per s
-
-
-
additional information
?
-
the purified yeast glucan synthase produces glucan with a length of 6550 plus/minus 760 mer. Pre-steady state kinetics analysis reveal a highly efficient but rate-determining chain elongation rate of 51.5 per s
-
-
-
additional information
?
-
involved in a late process of secondary or general septum synthesis, necessary to preserve cell integrity when cell wall synthesis or repair is needed
-
-
?
additional information
?
-
-
involved in a late process of secondary or general septum synthesis, necessary to preserve cell integrity when cell wall synthesis or repair is needed
-
-
?
additional information
?
-
-
bgs2p synthesizes linear beta-1,3-glucans, which remain unorganized and alkali-soluble untilcovalent linkages are set up between beta-1,3-glucans and other cell wall components involving beta-1,3-glucanosyltransferase activity, overview, bgs2p localizes to the spore periphery and is essential for maturation of the ascospore wall
-
-
?
additional information
?
-
-
linear (1,3)beta-D-glucan is the polysaccharide that specifically interacts with the fluorochrome Calcofluor white in fission yeast, the (1,3)beta-D-glucan synthase subunit Bgs1p is responsible for the fission yeast primary septum formation, Bgs1p is essential for vegetative cells and needed for correct septation and cell separation
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
additional information
?
-
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1,3)-beta-D-glucosyl]n
UDP + [(1,3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDP-glucose + [(1->3)-beta-D-glucosyl]n
UDP + [(1->3)-beta-D-glucosyl]n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
synthesis of callose in higher plants, enzyme is latent in intact and undamaged cells, it is activated only under perturbed conditions, possible involvement in wound-healing process and in defense against pathogens, enzyme seems to play a vital role in a number of specialized developmental processes in plants, namely pollen maturation and sieve pore formation and gravitropism
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
production of cell wall polysaccharide found in yeast cells
chain length 60-80
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
UDPglucose + (1,3-beta-D-glucosyl)n
UDP + (1,3-beta-D-glucosyl)n+1
-
-
-
?
additional information
?
-
-
main biosynthetic enzyme responsible for the callose response to biotic, abiotic, and chemical stresses, but not for callose deposition that is part of normal cell development. Enzyme negatively regulates salicylic acid defense signaling pathway
-
-
?
additional information
?
-
-
cell wall biosynthetic enzyme
-
-
?
additional information
?
-
-
the recombinant cytoplasmic domain binds specifically to UDP-agarose and lichenan (beta-glucan), but not to ADP-agarose, GDP-agarose, or other carbohydrates
-
-
?
additional information
?
-
-
cell wall biosynthetic enzyme
-
-
?
additional information
?
-
involved in a late process of secondary or general septum synthesis, necessary to preserve cell integrity when cell wall synthesis or repair is needed
-
-
?
additional information
?
-
-
involved in a late process of secondary or general septum synthesis, necessary to preserve cell integrity when cell wall synthesis or repair is needed
-
-
?
additional information
?
-
-
bgs2p synthesizes linear beta-1,3-glucans, which remain unorganized and alkali-soluble untilcovalent linkages are set up between beta-1,3-glucans and other cell wall components involving beta-1,3-glucanosyltransferase activity, overview, bgs2p localizes to the spore periphery and is essential for maturation of the ascospore wall
-
-
?
additional information
?
-
-
linear (1,3)beta-D-glucan is the polysaccharide that specifically interacts with the fluorochrome Calcofluor white in fission yeast, the (1,3)beta-D-glucan synthase subunit Bgs1p is responsible for the fission yeast primary septum formation, Bgs1p is essential for vegetative cells and needed for correct septation and cell separation
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
(1R,3R,6aS,7R,8R,10bR,12aR)-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-2-[[(2R)-1-methylpyrrolidin-2-yl]methoxy]-3-[5-(pyridin-4-yl)-1H-1,2,4-triazol-1-yl]-1,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-2H-1,4a-(methanooxymethano)chrysene-7-carboxylic acid
-
IC50: 19 ng/ml, pH and temperature not specified in the publication
(1R,3R,6aS,7R,8R,10bR,12aR)-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-2-[[(2R)-2-methylpyrrolidin-2-yl]methoxy]-3-[5-(pyridin-4-yl)-1H-1,2,4-triazol-1-yl]-1,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-2H-1,4a-(methanooxymethano)chrysene-7-carboxylic acid
-
IC50: 4 ng/ml, pH and temperature not specified in the publication
(1R,3R,6aS,7R,8R,10bR,12aR)-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-2-[[(2S)-1-methylpyrrolidin-2-yl]methoxy]-3-[5-(pyridin-4-yl)-1H-1,2,4-triazol-1-yl]-1,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-2H-1,4a-(methanooxymethano)chrysene-7-carboxylic acid
-
IC50: 61 ng/ml, pH and temperature not specified in the publication
(1R,3R,6aS,7R,8R,10bR,12aR)-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-3-[5-(pyridin-4-yl)-1H-1,2,4-triazol-1-yl]-2-[(2R)-pyrrolidin-2-ylmethoxy]-1,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-2H-1,4a-(methanooxymethano)chrysene-7-carboxylic acid
-
IC50: 22 ng/ml, pH and temperature not specified in the publication
(1R,3R,6aS,7R,8R,10bR,12aR)-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-3-[5-(pyridin-4-yl)-1H-1,2,4-triazol-1-yl]-2-[(2S)-pyrrolidin-2-ylmethoxy]-1,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-2H-1,4a-(methanooxymethano)chrysene-7-carboxylic acid
-
IC50: 18 ng/ml, pH and temperature not specified in the publication
(1R,3R,6aS,7R,8R,10bR,12aR)-2-[[(2R)-1,2-dimethylpyrrolidin-2-yl]methoxy]-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-3-[5-(pyridin-4-yl)-1H-1,2,4-triazol-1-yl]-1,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-2H-1,4a-(methanooxymethano)chrysene-7-carboxylic acid
-
IC50: 6.4 ng/ml, pH and temperature not specified in the publication
(1R,6aS,7R,8R,10bR,12aR)-1,6a,8,10a-tetramethyl-8-[(2R)-3-methylbutan-2-yl]-3-[5-(pyridin-4-yl)-1H-1,2,4-triazol-1-yl]-2-[[(2R)-2,3,3-trimethyl-2-(methylamino)butyl]oxy]-1,3,4,6,6a,7,8,9,10,10a,10b,11,12,12a-tetradecahydro-2H-1,4a-(methanooxymethano)chrysene-7-carboxylic acid
-
IC50: 2 ng/ml, pH and temperature not specified in the publication
(2,6-difluoro-phenyl)-carbamic acid 3-(4-benzothiazol-2-yl-piperazine-1-yl)-propyl ester
-
The piperazine propanol derivative GS1578 was identified as a potent inhibitor against 1,3-beta-D-glucan synthase, IC50: 0.16 microM.
1,2-Bis(O-aminophenoxy)ethane-N,N,N',N'-tetraacetate
-
-
Acylcarnitine
-
inhibition in presence of digitonin, stimulation in absence of digitonin within a certain concentration range
anidulafungin
-
an antifungal echinocandin drug, inhibition profile of wild-type and mutant enzymes
Congo red
-
non competitive
D-glucono-1,5-lactone
-
-
dihydrosphingosine
-
non-competitive inhibition
enfumafungin
-
IC50: 40 microgram/ml, pH 7.5, temperature not specified
Glycylglycine buffer
-
0.75 M
lysophosphatidylcholine
-
inhibition in presence of digitonin, stimulation in absence of digitonin within a certain concentration range
Mg2+
-
1,3-beta-glucan synthase 1
micafungin
-
an antifungal echinocandin drug, inhibition profile of wild-type and mutant enzymes
monomeric single-chain variable fragment (scFv)
-
Natural inhibitor in green Euglena cells
-
-
-
orizabin IX
-
IC50: 0.181 mg/ml
orizabin V
-
IC50: 0.155 mg/ml
orizabin X
-
IC50: 0.070 mg/ml
orizabin XI
-
IC50: 0.072 mg/ml
orizabin XIV
-
IC50: 0.074 mg/ml
orizabin XIX
-
IC50: 0.062 mg/ml
orizabin XV
-
IC50: 0.149 mg/ml
orizabin XVII
-
IC50: 0.078 mg/ml
orizabin XX
-
IC50: 0.065 mg/ml
p-chloromercuribenzoate
-
-
p-hydroxymercuribenzoate
-
-
papulacandin
-
IC50: 0.02 microgram/ml, pH 7.5, temperature not specified
Phospholipase A2
-
fatty acids and lysophospholipids are the inhibitory moieties
-
Phospholipase C
-
fatty acids and lysophospholipids are the inhibitory moieties
-
phytosphingosine
-
non-competitive inhibition
platelet-activating factor
-
inhibition in presence of digitonin, stimulation in absence of digitonin within a certain concentration range
pneumocandin
-
IC50: 120 microgram/ml, pH 7.5, temperature not specified
Sirofluor
-
fluorochrome from aniline blue
-
tricolorin A
-
IC50: 0.085 mg/ml
tricolorin B
-
IC50: 0.132 mg/ml
tricolorin C
-
IC50: 0.135 mg/ml
tricolorin D
-
IC50: 0.087 mg/ml
tricolorin E
-
IC50: 0.099 mg/ml
tricolorin F
-
IC50: more than 0.250 mg/ml
tricolorin I
-
IC50: 0.106 mg/ml
unsaturated fatty acids
-
trienoic acids most effective
-
ATP
-
-
ATP
-
both 1,3-beta-glucan synthases
Ca2+
-
at high concentration, stimulation at low concentration
Ca2+
-
1,3-beta-glucan synthase 1
caspofungin
-
-
caspofungin
-
50% inhibition at 0.00013 mg/ml
caspofungin
treatment with caspofungin at either the growth-inhibitory concentration (0.5 microg/ml) or paradoxical growth-inducing concentration (4 microg/ml) for 24 h causes similar abnormalities, including wider, hyperbranched hyphae, increased septation, and repeated hyphal tip lysis, followed by regenerative intrahyphal growth. At both concentrations, Fks1 initially mislocalizes from the hyphal tips to vacuoles. Only continuous exposure to 4 microg/ml of caspofungin for 48 h leads to recovery of the normal hyphal morphology with renewed localization of Fks1 to hyphal tips. Farnesol blocks paradoxical growth and relocalizes Fks1 and regulatory subunit Rho1 to vacuoles
caspofungin
-
very high caspofungin concentrations exert an additional antifungal activity besides inhibition of the beta-1,3-glucan synthase. Exposure to inhibitory caspofungin concentrations causes initial growth deprivation independently of the capability of the drug concentration to induce the paradoxical effect, i.e. the resumption of growth of otherwise susceptible strains at higher drug concentrations. Paradoxically growing hyphae emerge from microcolonies essentially devoid of beta-1,3-glucan. These hyphae expose beta-1,3-glucan again, suggesting that beta-1,3-glucan synthesis is restored. Expression of the beta-1,3-glucan synthase Fks1 is an essential requirement for the paradoxical effect. Overexpression of Fks1 renders Emericella nidulans more susceptible, whereas reduced expression leads to hyphae that are more resistant to the growth-inhibitory and limited fungicidal activity of caspofungin
caspofungin
-
exposure of strain RG101 to caspofungin during growth yields a modified enzyme that is drug insensitive (4 log orders) in kinetic inhibition assays, and this insensitivity is also observed for enzymes isolated from clinical isolates. The lipid microenvironment of the enzyme with resistance induced by caspofungin reveals a prominent increase in the abundances of dihydrosphingosine and phytosphingosine. Exogenous addition of dihydrosphingosine and phytosphingosine to the sensitive enzyme recapitulates the drug insensitivity of the caspofungin-derived enzyme. Caspofungin induces mitochondrion-derived reactive oxygen species, and dampening reactive oxygen species formation by antimycin A or thiourea eliminates drug-induced resistance
caspofungin
-
50% inhibition at 0.016 mg/ml
caspofungin
-
50% inhibition at 0.004 mg/ml
caspofungin
-
50% inhibition at 0.00013 mg/ml
caspofungin
-
IC50: 0.3 microgram/ml, pH 7.5, temperature not specified
caspofungin
-
an antifungal echinocandin drug, inhibition profile of wild-type and mutant enzymes
Caspofungin acetate
-
IC50: 30nM
cilofungin
-
maximal inhibition at 1.25 mM is 80%; non-competitive inhibition
cilofungin
-
non-competitive inhibition
cilofungin
-
50% inhibition at 0.064 mg/ml
Echinocandin B
-
-
Echinocandin B
-
inhibition in presence of digitonin, stimulation in absence of digitonin within a certain concentration range
EDTA
-
fully reversible by addition of Ca2+
EGTA
-
fully reversible by addition of Ca2+
ethanol
-
-
GTP
-
-
GTP
-
both 1,3-beta-glucan synthases
HM-1
-
HM-1 inhibits the growth of yeast cells by forming a pore at the growing tip of the daughter cell, resulting in the formation of a protruding structure and eventual cell death.
-
HM-1
-
HM-1 inhibits the growth of yeast cells by forming a pore at the growing tip of the daughter cell, resulting in the formation of a protruding structure and eventual cell death.
-
HM-1
-
HM-1 inhibits the growth of yeast cells by forming a pore at the growing tip of the daughter cell, resulting in the formation of a protruding structure and eventual cell death.
-
HM-1
-
HM-1 inhibits the growth of yeast cells by forming a pore at the growing tip of the daughter cell, resulting in the formation of a protruding structure and eventual cell death.
-
HM-1
-
HM-1 inhibits the growth of yeast cells by forming a pore at the growing tip of the daughter cell, resulting in the formation of a protruding structure and eventual cell death.
-
MK 991
-
-
Mn2+
-
at high concentration, stimulation at low concentration
Mn2+
-
1,3-beta-glucan synthase 1
monomeric single-chain variable fragment (scFv)
-
All four scFvs (scFv-A1, scFv-A2, scFv-A3, scFv-A4) inhibit beta-1,3-glucan-synthase. Most cultured cells treated with scFvs (3h) have a pearlike structure with protruding materials, characteristic of pore formation and similar to the morphology change after treatment with HM-1. These clearly indicate that the scFvs appear to have the same effect as HM-1 on sensitive yeast cells.
-
monomeric single-chain variable fragment (scFv)
-
All four scFvs (scFv-A1, scFv-A2, scFv-A3, scFv-A4) inhibit beta-1,3-glucan-synthase. Most cultured cells treated with scFvs (3h) have a pearlike structure with protruding materials, characteristic of pore formation and similar to the morphology change after treatment with HM-1. These clearly indicate that the scFvs appear to have the same effect as HM-1 on sensitive yeast cells.
-
monomeric single-chain variable fragment (scFv)
-
All four scFvs (scFv-A1, scFv-A2, scFv-A3, scFv-A4) inhibit beta-1,3-glucan-synthase. Most cultured cells treated with scFvs (3h) have a pearlike structure with protruding materials, characteristic of pore formation and similar to the morphology change after treatment with HM-1. These clearly indicate that the scFvs appear to have the same effect as HM-1 on sensitive yeast cells.
-
monomeric single-chain variable fragment (scFv)
-
All four scFvs (scFv-A1, scFv-A2, scFv-A3, scFv-A4) inhibit beta-1,3-glucan-synthase. Most cultured cells treated with scFvs (3h) have a pearlike structure with protruding materials, characteristic of pore formation and similar to the morphology change after treatment with HM-1. These clearly indicate that the scFvs appear to have the same effect as HM-1 on sensitive yeast cells.
-
monomeric single-chain variable fragment (scFv)
-
All four scFvs (scFv-A1, scFv-A2, scFv-A3, scFv-A4) inhibit beta-1,3-glucan-synthase. Most cultured cells treated with scFvs (3h) have a pearlike structure with protruding materials, characteristic of pore formation and similar to the morphology change after treatment with HM-1. These clearly indicate that the scFvs appear to have the same effect as HM-1 on sensitive yeast cells.
-
N-ethylmaleimide
-
0.16 mM, partial inhibition
N-ethylmaleimide
-
0.16 mM, partial inhibition
N-ethylmaleimide
-
0.16 mM, partial inhibition
N-ethylmaleimide
-
0.16 mM, partial inhibition
N-ethylmaleimide
-
0.16 mM, partial inhibition
N-ethylmaleimide
-
0.16 mM, partial inhibition
oryzalin
-
-
papulacandin B
-
-
papulacandin B
-
IC50: 0.1 mg/ml
Showdomycin
-
0.1 mM, partial inhibition
Showdomycin
-
0.1 mM, partial inhibition
Showdomycin
-
0.1 mM, partial inhibition
Showdomycin
-
0.1 mM, partial inhibition
Showdomycin
-
0.1 mM, partial inhibition
Showdomycin
-
0.1 mM, partial inhibition
Triton X-100
-
-
UDP
-
-
UMP
-
-
UTP
-
-
additional information
-
Preincubation with nMAb-KT eliminate the inhibition of Candida growth by scFv antibodies, suggestig that the observed cytocidal effect of scFv antibodies is due to their structural resemblance to HM-1.
-
additional information
-
enzyme activity is inhibited by ethanol extract of Salvia miltiorrhiza
-
additional information
-
Preincubation with nMAb-KT eliminate the inhibition of Candida growth by scFv antibodies, suggestig that the observed cytocidal effect of scFv antibodies is due to their structural resemblance to HM-1.
-
additional information
-
Preincubation with nMAb-KT eliminate the inhibition of Candida growth by scFv antibodies, suggestig that the observed cytocidal effect of scFv antibodies is due to their structural resemblance to HM-1.
-
additional information
-
not inhibited by caspofungin acetate (CFA)
-
additional information
-
the somatic isozyme is inactivated by trypsin, in contrast to the pollen isozyme
-
additional information
-
Preincubation with nMAb-KT eliminate the inhibition of Candida growth by scFv antibodies, suggestig that the observed cytocidal effect of scFv antibodies is due to their structural resemblance to HM-1.
-
additional information
-
Preincubation with nMAb-KT eliminate the inhibition of Candida growth by scFv antibodies, suggestig that the observed cytocidal effect of scFv antibodies is due to their structural resemblance to HM-1.
-
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Drc1p/Cps1p, a 1,3-beta-glucan synthase subunit, is essential for division septum assembly in Schizosaccharomyces pombe
Genetics
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Schizosaccharomyces pombe
brenda
Mulichak, A.M.; Losey, H.C.; Walsh, C.T.; Garavito, R.M.
Structure of the UDP-glucosyltransferase GtfB that modifies the heptapeptide aglycone in the biosynthesis of vancomycin group antibiotics
Structure
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Staphylococcus aureus
brenda
Maligie, M.A.; Selitrennikoff, C.P.
Cryptococcus neoformans resistance to echinocandins: (1,3)beta-glucan synthase activity is sensitive to echinocandins
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Aspergillus fumigatus, Saccharomyces cerevisiae, Cryptococcus neoformans, Neurospora crassa
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Schimoler-O'Rourke, R.; Renault, S.; Mo, W.; Selitrennikoff, C.P.
Neurospora crassa FKS protein binds to the (1,3)beta-glucan synthase substrate, UDP-glucose
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Neurospora crassa
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Karnezis, T.; Epa, V.C.; Stone, B.A.; Stanisich, V.A.
Topological characterization of an inner membrane (1-->3)-beta-D-glucan (curdlan) synthase from Agrobacterium sp. strain ATCC31749
Glycobiology
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2003
Agrobacterium sp., Agrobacterium sp. ATCC 31749
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Fairweather, J.K.; Him, J.L.K.; Heux, L.; Driguez, H.; Bulone, V.
Structural characterization by 13C-NMR spectroscopy of products synthesized in vitro by polysaccharide synthases using 13C-enriched glycosyl donors: Application to a UDP-glucose:(1->3)-beta-D-glucan synthase from blackberry (Rubus fruticosus)
Glycobiology
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2004
Rubus plicatus
brenda
Cortes, J.C.; Carnero, E.; Ishiguro, J.; Sanchez, Y.; Duran, A.; Ribas, J.C.
The novel fission yeast (1,3)beta-D-glucan synthase catalytic subunit Bgs4p is essential during both cytokinesis and polarized growth
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Schizosaccharomyces pombe (O74475), Schizosaccharomyces pombe
brenda
Jacobs, A.K.; Lipka, V.; Burton, R.A.; Panstruga, R.; Strizhov, N.; Schulze-Lefert, P.; Fincher, G.B.
An Arabidopsis callose synthase, GSL5, is required for wound and papillary callose formation
Plant Cell
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Arabidopsis thaliana
brenda
Dong, X.; Hong, Z.; Sivaramakrishnan, M.; Mahfouz, M.; Verma, D.P.
Callose synthase (CalS5) is required for exine formation during microgametogenesis and for pollen viability in Arabidopsis
Plant J.
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Arabidopsis thaliana
brenda
Nishimura, M.T.; Stein, M.; Hou, B.H.; Vogel, J.P.; Edwards, H.; Somerville, S.C.
Loss of a callose synthase results in salicylic acid-dependent disease resistance
Science
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Arabidopsis thaliana
brenda
Selvakumar, D.; Miyamoto, M.; Furuichi, Y.; Komiyama, T.
Inhibition of fungal beta-1,3-glucan synthase and cell growth by HM-1 killer toxin single-chain anti-idiotypic antibodies
Antimicrob. Agents Chemother.
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Saccharomyces cerevisiae, Candida albicans, [Candida] glabrata, Candida parapsilosis, Candida tropicalis
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Kondoh, O.; Inagaki, Y.; Fukuda, H.; Mizuguchi, E.; Ohya, Y.; Arisawa, M.; Shimma, N.; Aoki, Y.; Sakaitani, M.; Watanabe, T.
Piperazine propanol derivative as a novel antifungal targeting 1,3-beta-D-glucan synthase
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Saccharomyces cerevisiae, Candida albicans
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Yamaguchi, T.; Hayashi, T.; Nakayama, K.; Koike, S.
Expression analysis of genes for callose synthases and Rho-type small GTP-binding proteins that are related to callose synthesis in rice anther
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Oryza sativa
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Nishikawa, S.; Zinkl, G.M.; Swanson, R.J.; Maruyama, D.; Preuss, D.
Callose (beta-1,3 glucan) is essential for Arabidopsis pollen wall patterning, but not tube growth
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Arabidopsis thaliana
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Kellner, E.M.; Orsborn, K.I.; Siegel, E.M.; Mandel, M.A.; Orbach, M.J.; Galgiani, J.N.
Coccidioides posadasii contains a single 1,3-beta-glucan synthase gene that appears to be essential for growth
Eukaryot. Cell
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Coccidioides posadasii
brenda
Ha, Y.S.; Covert, S.F.; Momany, M.
FsFKS1, the 1,3-beta-glucan synthase from the caspofungin-resistant fungus Fusarium solani
Eukaryot. Cell
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Aspergillus fumigatus, Candida albicans, Fusarium solani
brenda
Ishihara, S.; Hirata, A.; Nogami, S.; Beauvais, A.; Latge, J.P.; Ohya, Y.
Homologous subunits of 1,3-beta-glucan synthase are important for spore wall assembly in Saccharomyces cerevisiae
Eukaryot. Cell
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Saccharomyces cerevisiae
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Enns, L.C.; Kanaoka, M.M.; Torii, K.U.; Comai, L.; Okada, K.; Cleland, R.E.
Two callose synthases, GSL1 and GSL5, play an essential and redundant role in plant and pollen development and in fertility
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Arabidopsis thaliana
brenda
Voigt, C.A.; Schaefer, W.; Salomon, S.
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Triticum aestivum
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Huang, L.S.; Doherty, H.K.; Herskowitz, I.
The Smk1p MAP kinase negatively regulates Gsc2p, a 1,3-beta-glucan synthase, during spore wall morphogenesis in Saccharomyces cerevisiae
Proc. Natl. Acad. Sci. USA
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Saccharomyces cerevisiae
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Cortes, J.C.; Konomi, M.; Martins, I.M.; Munoz, J.; Moreno, M.B.; Osumi, M.; Duran, A.; Ribas, J.C.
The (1,3)beta-D-glucan synthase subunit Bgs1p is responsible for the fission yeast primary septum formation
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Schizosaccharomyces pombe
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de Medina-Redondo, M.; Arnaiz-Pita, Y.; Fontaine, T.; Del Rey, F.; Latge, J.P.; Vazquez de Aldana, C.R.
The beta-1,3-glucanosyltransferase gas4p is essential for ascospore wall maturation and spore viability in Schizosaccharomyces pombe
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Schizosaccharomyces pombe
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Saheed, S.A.; Cierlik, I.; Larsson, K.A.; Delp, G.; Bradley, G.; Jonsson, L.M.; Botha, C.E.
Stronger induction of callose deposition in barley by Russian wheat aphid than bird cherry-oat aphid is not associated with differences in callose synthase or beta-1,3-glucanase transcript abundance
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Hordeum vulgare
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Schuette, S.; Wood, A.J.; Geisler, M.; Geisler-Lee, J.; Ligrone, R.; Renzaglia, K.S.
Novel localization of callose in the spores of Physcomitrella patens and phylogenomics of the callose synthase gene family
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Garcia-Effron, G.; Lee, S.; Park, S.; Cleary, J.D.; Perlin, D.S.
Effect of Candida glabrata FKS1 and FKS2 mutations on echinocandin sensitivity and kinetics of 1,3-beta-D-glucan synthase: implication for the existing susceptibility breakpoint
Antimicrob. Agents Chemother.
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[Candida] glabrata
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Brownfield, L.; Wilson, S.; Newbigin, E.; Bacic, A.; Read, S.
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Aidemark, M.; Andersson, C.; Rasmusson, A.; Widell, S.
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Arabidopsis thaliana, Nicotiana tabacum, Arabidopsis thaliana Col-0
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Okada, H.; Abe, M.; Asakawa-Minemura, M.; Hirata, A.; Qadota, H.; Morishita, K.; Ohnuki, S.; Nogami, S.; Ohya, Y.
Multiple functional domains of the yeast 1,3-beta-glucan synthase subunit Fks1p revealed by quantitative phenotypic analysis of temperature-sensitive mutants
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Saccharomyces cerevisiae
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Schober, M.S.; Burton, R.A.; Shirley, N.J.; Jacobs, A.K.; Fincher, G.B.
Analysis of the (1,3)-beta-D-glucan synthase gene family of barley
Phytochemistry
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Chen, X.Y.; Liu, L.; Lee, E.; Han, X.; Rim, Y.; Chu, H.; Kim, S.W.; Sack, F.; Kim, J.Y.
The Arabidopsis callose synthase gene GSL8 is required for cytokinesis and cell patterning
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Arabidopsis thaliana
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Dong, X.; Hong, Z.; Chatterjee, J.; Kim, S.; Verma, D.P.
Expression of callose synthase genes and its connection with Npr1 signaling pathway during pathogen infection
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Arabidopsis thaliana
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Heasley, B.H.; Pacofsky, G.J.; Mamai, A.; Liu, H.; Nelson, K.; Coti, G.; Peel, M.R.; Balkovec, J.M.; Greenlee, M.L.; Liberator, P.; Meng, D.; Parker, D.L.; Wilkening, R.R.; Apgar, J.M.; Racine, F.; Hsu, M.J.; Giacobbe, R.A.; Kahn, J.N.
Synthesis and biological evaluation of antifungal derivatives of enfumafungin as orally bioavailable inhibitors of beta-1,3-glucan synthase
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Candida albicans
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Ujita, M.; Inoue, R.; Makino, Y.; Katsuno, Y.; Okumura, H.
Binding specificity of the recombinant cytoplasmic domain of Cordyceps militaris beta-1,3-glucan synthase catalytic subunit
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Cordyceps militaris
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Yang, M.; Jin, K.; Xia, Y.
MaFKS, a beta-1,3-glucan synthase, is involved in cell wall integrity, hyperosmotic pressure tolerance and conidiation in Metarhizium acridum
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Metarhizium acridum
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Tomazett, P.K.; Felix, C.R.; Lenzi, H.L.; de Paula Faria, F.; de Almeida Soares, C.M.; Pereira, M.
1,3-beta-D-Glucan synthase of Paracoccidioides brasiliensis: recombinant protein, expression and cytolocalization in the yeast and mycelium phases
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Paracoccidioides brasiliensis
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Hrmova, M.; Stone, B.A.; Fincher, G.B.
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Martins, I.M.; Cortes, J.C.; Munoz, J.; Moreno, M.B.; Ramos, M.; Clemente-Ramos, J.A.; Duran, A.; Ribas, J.C.
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Anjos, J.; Fernandes, C.; Silva, B.M.; Quintas, C.; Abrunheiro, A.; Gow, N.A.; Goncalves, T.
beta(1,3)-glucan synthase complex from Alternaria infectoria, a rare dematiaceous human pathogen
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Alternaria infectoria
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Sanchez-Leon, E.; Riquelme, M.
Live imaging of beta-1,3-glucan synthase FKS-1 in Neurospora crassa hyphae
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Neurospora crassa (Q7S0A7), Neurospora crassa
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Lee, H.S.; Kim, Y.
Antifungal activity of Salvia miltiorrhiza against Candida albicans is associated with the alteration of membrane permeability and (1,3)-beta-D-glucan synthase activity
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Candida albicans, Candida albicans ATCC 18804
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Yang, Y.H.; Kang, H.W.; Ro, H.S.
Cloning and molecular characterization of beta-1,3-glucan synthase from Sparassis crispa
Mycobiology
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167-173
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Sparassis crispa (A0A076VIT3), Sparassis crispa IUM4010 (A0A076VIT3)
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Oliveira-Garcia, E.; Deising, H.B.
Infection structure-specific expression of beta-1,3-glucan synthase is essential for pathogenicity of Colletotrichum graminicola and evasion of beta-glucan-triggered immunity in maize
Plant Cell
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Colletotrichum graminicola (E3QI14)
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Moreno-Velasquez, S.D.; Seidel, C.; Juvvadi, P.R.; Steinbach, W.J.; Read, N.D.
Caspofungin-mediated growth inhibition and paradoxical growth in Aspergillus fumigatus involve fungicidal hyphal tip lysis coupled with regenerative intrahyphal growth and dynamic changes in beta-1,3-glucan synthase localization
Antimicrob. Agents Chemother.
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Aspergillus fumigatus (P87204)
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Loiko, V.; Wagener, J.
The paradoxical effect of echinocandins in Aspergillus fumigatus relies on recovery of the beta-1,3-glucan synthase Fks1
Antimicrob. Agents Chemother.
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Aspergillus fumigatus, Aspergillus fumigatus AfS35
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Luraschi, A.; Richard, S.; Hauser, P.M.
Site-directed mutagenesis of the 1,3-beta-glucan synthase catalytic subunit of Pneumocystis jirovecii and susceptibility assays suggest its sensitivity to caspofungin
Antimicrob. Agents Chemother.
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e01159
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Pneumocystis carinii (Q9HEZ4), Pneumocystis jirovecii (L0PD34), Pneumocystis jirovecii SE8 (L0PD34), Pneumocystis murina (M7P3D9), Pneumocystis murina B123 (M7P3D9)
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Chhetri, A.; Loksztejn, A.; Nguyen, H.; Pianalto, K.M.; Kim, M.J.; Hong, J.; Alspaugh, J.A.; Yokoyama, K.
Length specificity and polymerization mechanism of (1,3)-beta-D-glucan synthase in fungal cell wall biosynthesis
Biochemistry
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682-693
2020
Saccharomyces cerevisiae (P40989), Saccharomyces cerevisiae ATCC 204508 (P40989)
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Schuster, M.; Guiu-Aragones, C.; Steinberg, G.
Class V chitin synthase and beta(1,3)-glucan synthase co-travel in the same vesicle in Zymoseptoria tritici
Fungal Genet. Biol.
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103286
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Zymoseptoria tritici (A0A2H1H497), Zymoseptoria tritici ST99CH_1E4 (A0A2H1H497)
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Satish, S.; Jimenez-Ortigosa, C.; Zhao, Y.; Lee, M.; Dolgov, E.; Krueger, T.; Park, S.; Denning, D.; Kniemeyer, O.; Brakhage, A.; Perlin, D.
Stress-induced changes in the lipid microenvironment of beta-(1,3)-D-glucan synthase cause clinically important echinocandin resistance in Aspergillus fumigatus
mBio
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Aspergillus nidulans, Aspergillus nidulans RG101
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