Species | Hemileia vastatrix | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Basidiomycota; Pucciniomycetes; ; Zaghouaniaceae; Hemileia; Hemileia vastatrix | |||||||||||
CAZyme ID | HVAS_10802461.1-p1 | |||||||||||
CAZy Family | GT58 | |||||||||||
CAZyme Description | unspecified product | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location |
EC | 2.4.1.142:10 | 2.4.1.-:1 |
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Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT33 | 8 | 293 | 3e-89 | 0.6047058823529412 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
340843 | GT33_ALG1-like | 1.72e-103 | 8 | 293 | 103 | 347 | chitobiosyldiphosphodolichol beta-mannosyltransferase and similar proteins. This family is most closely related to the GT33 family of glycosyltransferases. The yeast gene ALG1 has been shown to function as a mannosyltransferase that catalyzes the formation of dolichol pyrophosphate (Dol-PP)-GlcNAc2Man from GDP-Man and Dol-PP-Glc-NAc2, and participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. In humans ALG1 has been associated with the congenital disorders of glycosylation (CDG) designated as subtype CDG-Ik. |
215155 | PLN02275 | 1.10e-73 | 1 | 292 | 90 | 341 | transferase, transferring glycosyl groups |
340816 | Glycosyltransferase_GTB-type | 0.001 | 179 | 287 | 118 | 214 | glycosyltransferase family 1 and related proteins with GTB topology. Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. The structures of the formed glycoconjugates are extremely diverse, reflecting a wide range of biological functions. The members of this family share a common GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
2.20e-80 | 8 | 293 | 49 | 327 | |
3.60e-78 | 8 | 293 | 151 | 418 | |
2.01e-77 | 8 | 293 | 151 | 418 | |
6.71e-77 | 8 | 293 | 54 | 321 | |
7.92e-77 | 8 | 293 | 151 | 418 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
4.19e-58 | 8 | 293 | 132 | 395 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Mus musculus OX=10090 GN=Alg1 PE=1 SV=3 |
|
1.18e-56 | 8 | 293 | 132 | 395 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Homo sapiens OX=9606 GN=ALG1 PE=1 SV=2 |
|
3.27e-56 | 8 | 293 | 132 | 395 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Pongo abelii OX=9601 GN=ALG1 PE=2 SV=1 |
|
1.33e-53 | 8 | 293 | 115 | 386 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Dictyostelium discoideum OX=44689 GN=alg1 PE=2 SV=1 |
|
1.27e-50 | 8 | 292 | 109 | 387 | UDP-glycosyltransferase TURAN OS=Arabidopsis thaliana OX=3702 GN=TUN PE=2 SV=1 |
Other | SP_Sec_SPI | CS Position |
---|---|---|
0.999956 | 0.000110 |
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