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.
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
-
-
-
-
?
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
Q2QJ12
-
-
-
?
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
Q2QJ12
-
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
-
-
-
-
?
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
Q2QJ12
-
-
-
?
S-adenosyl-L-methionine + a (4E,8E)-sphinga-4,8-dienine ceramide
S-adenosyl-L-homocysteine + a 9-methyl-(4E,8E)-sphinga-4,8-dienine ceramide
Q2QJ12
-
-
-
?
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.
evolution
-
C-9-methylated glucosylceramides (GlcCers) are sphingolipids unique to fungi
evolution
Q2QJ12
the enzyme belongs to the superfamily of S-adenosylmethionine-dependent methyltransferases and shows highest sequence similarity to plant and bacterial cyclopropane fatty acid synthases, genetic organization and clustering of SAM-dependent methyltransferase sequences, phylogenetic profiling of SAM-dependent methyltransferases, overview
evolution
-
the enzyme belongs to the superfamily of S-adenosylmethionine-dependent methyltransferases and shows highest sequence similarity to plant and bacterial cyclopropane fatty acid synthases, genetic organization and clustering of SAM-dependent methyltransferase sequences, phylogenetic profiling of SAM-dependent methyltransferases, overview
-
evolution
-
C-9-methylated glucosylceramides (GlcCers) are sphingolipids unique to fungi
-
malfunction
Q2QJ12
a Pichia pastoris knock-out strain of the sphingolipid C9-methyltransferase lacks C9-methylated glucosylceramides
malfunction
-
the Candida albicans mts1 disruptant had a decreased hyphal growth rate compared to the wild-type strain. The mts1 disruptant grows similarly to wild-type in medium containing SDS or fluconazole. The membrane structure of the mts1 disruptant is not disturbed, mutant phenotype, overview
malfunction
-
the DELTAFgmt2 mutant exhibits severe growth defects and produces abnormal conidia, while the DELTAFgmt1 mutant grows like the wild-type strain. The DELTAFgmt2 mutant is less virulent on different host plants tested than the previously characterized DELTAFggcs1 mutant, which lacks GlcCer synthase activity and produces no GlcCer at all. Moreover, the DELTAFgmt1 and DELTAFgmt2 mutants retain sensitivity to the antifungal plant defensins MsDef1 and RsAFP2
malfunction
-
DELTAsmt1 mutants lacking the sphingolipid C9 methyltransferase gene (SMT1) are attenuated in virulence and have a growth defect at 37 °C, in neutral/alkaline pH and 5 % CO2 environments
malfunction
increased levels of unmethylated glucosylceramide are observed in smtA mutants. DELTAsmtA and wild-type cells show a similar 9-methyl-glucosylceramide content
malfunction
increased levels of unmethylated glucosylceramide are observed in smtB mutants. DELTAsmtB cells show activity reduced by 50%. The compromised 9-methyl-glucosylceramide production in the DELTAsmtB strain is not accompanied by reduced filamentation or defects in cell polarity
malfunction
-
a Pichia pastoris knock-out strain of the sphingolipid C9-methyltransferase lacks C9-methylated glucosylceramides
-
malfunction
-
the DELTAFgmt2 mutant exhibits severe growth defects and produces abnormal conidia, while the DELTAFgmt1 mutant grows like the wild-type strain. The DELTAFgmt2 mutant is less virulent on different host plants tested than the previously characterized DELTAFggcs1 mutant, which lacks GlcCer synthase activity and produces no GlcCer at all. Moreover, the DELTAFgmt1 and DELTAFgmt2 mutants retain sensitivity to the antifungal plant defensins MsDef1 and RsAFP2
-
metabolism
-
the enzyme is part of the C-9-methylated glucosylceramides biosynthesis pathway, overview
metabolism
-
the enzyme is part of the C-9-methylated glucosylceramides biosynthesis pathway, overview
-
physiological function
-
C9-methylated glucosylceramide is a fungus-specific sphingolipid. This lipid is a major membrane component in the cell and is thought to play important roles in the growth and virulence of several fungal species. The enzyme is involved in hyphal elongation. The C9-methyl group of a long-chain base in glucosylceramides plays an important role in the hyphal elongation of Candida albicans independent of lipid membrane disruption
physiological function
-
sphingolipid C-9 methyltransferases seem to be essential in the organism, they are important for growth and virulence but not for sensitivity to antifungal plant defensins in Fusarium graminearum. Isozyme FgMT2 encodes a sphingolipid C-9 methyltransferase that is capable of methylating C-9-methylated glucosylceramides in the absence of the FgMT1-encoded enzyme and that isozyme FgMT2 is the predominant sphingolipid C-9 methyltransferases for methylating C-9-methylated glucosylceramides
physiological function
-
the enzyme adds a methyl group to position nine of the sphingosine backbone of ceramide. The sphingolipid glucosylceramide and factors involved in the fungal GlcCer pathways are an integral part of fungal virulence, especially in fungal replication at 37 °C, in neutral/alkaline pH and 5 % CO2 environments (e.g. alveolar spaces)
physiological function
-
sphingolipid C-9 methyltransferases seem to be essential in the organism, they are important for growth and virulence but not for sensitivity to antifungal plant defensins in Fusarium graminearum. Isozyme FgMT2 encodes a sphingolipid C-9 methyltransferase that is capable of methylating C-9-methylated glucosylceramides in the absence of the FgMT1-encoded enzyme and that isozyme FgMT2 is the predominant sphingolipid C-9 methyltransferases for methylating C-9-methylated glucosylceramides
-
additional information
Q2QJ12
analysis of the sphingoid base composition of wild-type strains and Saccharomyces cerevisiae strain recombinantly expressing the enzyme
additional information
-
analysis of the sphingoid base composition of wild-type strains and Saccharomyces cerevisiae strain recombinantly expressing the enzyme
additional information
-
the C-9 methyl group is not a critical structural feature of the GlcCer receptor required for the antifungal action of plant defensins
additional information
-
analysis of the sphingoid base composition of wild-type strains and Saccharomyces cerevisiae strain recombinantly expressing the enzyme
-
additional information
-
the C-9 methyl group is not a critical structural feature of the GlcCer receptor required for the antifungal action of plant defensins
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
C9MT1_GIBZE
Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1)
513
1
58009
Swiss-Prot
other Location (Reliability: 4)
C9MT2_GIBZE
Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1)
521
3
59853
Swiss-Prot
other Location (Reliability: 2)
C9MT_CANAL
Candida albicans (strain SC5314 / ATCC MYA-2876)
513
2
58777
Swiss-Prot
other Location (Reliability: 2)
C9MT_KOMPG
Komagataella phaffii (strain GS115 / ATCC 20864)
489
1
56272
Swiss-Prot
other Location (Reliability: 4)
A0A8J5DVF3_9ASCO
512
2
58370
TrEMBL
other Location (Reliability: 2)
A0A8J8W7T8_9EURO
518
2
59030
TrEMBL
other Location (Reliability: 2)
A0A8J5EHF1_9ASCO
466
0
53338
TrEMBL
other Location (Reliability: 2)
A0A5K1JSU2_9APHY
162
0
18356
TrEMBL
other Location (Reliability: 2)
Q5AWF5_EMENI
Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139)
510
0
57750
TrEMBL
-
Q5B192_EMENI
Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139)
517
0
58155
TrEMBL
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
additional information
-
construction of a mts1 disruptant mutant strain MTS105 that lacks (E,E)-9-methylsphinga-4,8-dienine in its glucosylceramides and contains (E)-sphing-4-enine and (E,E)-sphinga-4,8-dienine. Reintroducing the MTS1 gene into the mts1 disruptant restores the synthesis of (E,E)-9-methylsphinga-4,8-dienine in the glucosylceramides
additional information
-
construction of enzyme knockout mutants of genes FgMT1 and FgMT2 by gene replacements, penotypes, overview. The DELTAFgmt1 mutant produces C-9-methylated GlcCer like the wild-type strain, whereas the DELTAFgmt2 mutant produces 65 to 75% nonmethylated and 25 to 35% methylated GlcCer. No DELTAFgmt1DELTAFgmt2 double-knockout mutant producing only nonmethylated GlcCer can be recovered,. The DELTAFgmt2 mutant exhibits drastically reduced disease symptoms when expressed in Triticum aestivum and much-delayed disease symptoms when expressed in Arabidopsis thaliana
additional information
-
construction of enzyme knockout mutants of genes FgMT1 and FgMT2 by gene replacements, penotypes, overview. The DELTAFgmt1 mutant produces C-9-methylated GlcCer like the wild-type strain, whereas the DELTAFgmt2 mutant produces 65 to 75% nonmethylated and 25 to 35% methylated GlcCer. No DELTAFgmt1DELTAFgmt2 double-knockout mutant producing only nonmethylated GlcCer can be recovered,. The DELTAFgmt2 mutant exhibits drastically reduced disease symptoms when expressed in Triticum aestivum and much-delayed disease symptoms when expressed in Arabidopsis thaliana
-
additional information
Q2QJ12
construction of a Pichia pastoris knock-out strain lacking sphingolipid C9-methyltransferase, the strain contains only non-methylated glucosylceramides
additional information
-
construction of a Pichia pastoris knock-out strain lacking sphingolipid C9-methyltransferase, the strain contains only non-methylated glucosylceramides
additional information
-
construction of a Pichia pastoris knock-out strain lacking sphingolipid C9-methyltransferase, the strain contains only non-methylated glucosylceramides
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
DNA and amino acid sequence determination and analysis, genetic organization and clustering of SAM-dependent methyltransferase sequences, phylogenetic tree, recombinant enzyme functional expression in a Saccharomyces cerevisiae strain that is engineered to produce glucosylceramides suitable as a substrate for C9-methylation. C9-methylated sphingolipids are detected in the transformed strain expressing the candidate from Pichia pastoris, demonstrating its function as a sphingolipid C9-methyltransferase
Q2QJ12
gene mts1, orf19.4831, cloning in Escherichia coli strain DH5alpha
-
genes FgMT1 and FgMT2, DNA and amino acid sequence determination and analysis, sequence comparisons, recombinant expression in and complementation of an enzyme knockout mutant strain C-9-MT-null of Pichia pastoris
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Ramamoorthy, V.; Cahoon, E.; Thokala, M.; Kaur, J.; Li, J.; Shah, D.
Sphingolipid C-9 methyltransferases are important for growth and virulence but not for sensitivity to antifungal plant defensins in Fusarium graminearum
Eukaryot. Cell
8
217-229
2009
Fusarium graminearum, Fusarium graminearum PH-1
brenda
Ternes, P.; Sperling, P.; Albrecht, S.; Franke, S.; Cregg, J.M.; Warnecke, D.; Heinz, E.
Identification of fungal sphingolipid C9-methyltransferases by phylogenetic profiling
J. Biol. Chem.
281
5582-5592
2006
Komagataella pastoris (Q2QJ12), Komagataella pastoris, Komagataella pastoris GS115 (Q2QJ12)
brenda
Oura, T.; Kajiwara, S.
Candida albicans sphingolipid C9-methyltransferase is involved in hyphal elongation
Microbiology
156
1234-1243
2010
Candida albicans
brenda
Singh, A.; Rella, A.; Schwacke, J.; Vacchi-Suzzi, C.; Luberto, C.; Del Poeta, M.
Transmembrane transporter expression regulated by the glucosylceramide pathway in Cryptococcus neoformans
BMC Res. Notes
8
861
2015
Cryptococcus neoformans var. grubii
brenda
Fernandes, C.; de Castro, P.; Singh, A.; Fonseca, F.; Pereira, M.; Vila, T.; Atella, G.; Rozental, S.; Savoldi, M.; Del Poeta, M.; Goldman, G.; Kurtenbach, E.
Functional characterization of the Aspergillus nidulans glucosylceramide pathway reveals that LCB DELTA8-desaturation and C9-methylation are relevant to filamentous growth, lipid raft localization and Psd1 defensin activity
Mol. Microbiol.
102
488-505
2016
Aspergillus nidulans (Q5AWF5), Aspergillus nidulans (Q5B192)
brenda