Species | Podospora anserina | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Ascomycota; Sordariomycetes; ; Podosporaceae; Podospora; Podospora anserina | |||||||||||
CAZyme ID | XP_001904656.1 | |||||||||||
CAZy Family | AA9 | |||||||||||
CAZyme Description | 1,3-beta-D-glucan-UDP glucosyltransferase [Source:UniProtKB/TrEMBL;Acc:B2AKS5] | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location |
EC | 2.4.1.34:56 |
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Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT48 | 880 | 1657 | 0 | 0.986468200270636 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
396784 | Glucan_synthase | 0.0 | 880 | 1705 | 1 | 819 | 1,3-beta-glucan synthase component. This family consists of various 1,3-beta-glucan synthase components including Gls1, Gls2 and Gls3 from yeast. 1,3-beta-glucan synthase EC:2.4.1.34 also known as callose synthase catalyzes the formation of a beta-1,3-glucan polymer that is a major component of the fungal cell wall. The reaction catalyzed is:- UDP-glucose + {(1,3)-beta-D-glucosyl}(N) <=> UDP + {(1,3)-beta-D-glucosyl}(N+1). |
405046 | FKS1_dom1 | 1.75e-48 | 365 | 474 | 1 | 111 | 1,3-beta-glucan synthase subunit FKS1, domain-1. The FKS1_dom1 domain is likely to be the 'Class I' region just N-terminal to the first set of transmembrane helices that is involved in 1,3-beta-glucan synthesis itself. This family is found on proteins with family Glucan_synthase, pfam02364. |
133045 | CESA_like | 3.02e-04 | 1125 | 1258 | 38 | 171 | CESA_like is the cellulose synthase superfamily. The cellulose synthase (CESA) superfamily includes a wide variety of glycosyltransferase family 2 enzymes that share the common characteristic of catalyzing the elongation of polysaccharide chains. The members include cellulose synthase catalytic subunit, chitin synthase, glucan biosynthesis protein and other families of CESA-like proteins. Cellulose synthase catalyzes the polymerization reaction of cellulose, an aggregate of unbranched polymers of beta-1,4-linked glucose residues in plants, most algae, some bacteria and fungi, and even some animals. In bacteria, algae and lower eukaryotes, there is a second unrelated type of cellulose synthase (Type II), which produces acylated cellulose, a derivative of cellulose. Chitin synthase catalyzes the incorporation of GlcNAc from substrate UDP-GlcNAc into chitin, which is a linear homopolymer of beta-(1,4)-linked GlcNAc residues and Glucan Biosynthesis protein catalyzes the elongation of beta-1,2 polyglucose chains of Glucan. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
0.0 | 1 | 1960 | 1 | 1960 | |
0.0 | 1 | 1960 | 1 | 1960 | |
0.0 | 1 | 1960 | 1 | 1958 | |
0.0 | 133 | 1960 | 112 | 1932 | |
0.0 | 135 | 1960 | 114 | 1926 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
0.0 | 221 | 1942 | 15 | 1777 | 1,3-beta-glucan synthase component FKS3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) OX=559292 GN=FKS3 PE=1 SV=1 |
|
0.0 | 131 | 1946 | 87 | 1895 | 1,3-beta-glucan synthase component FKS1 OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) OX=425011 GN=fksA PE=3 SV=1 |
|
0.0 | 136 | 1927 | 96 | 1874 | 1,3-beta-glucan synthase component GSC2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) OX=559292 GN=GSC2 PE=1 SV=2 |
|
0.0 | 183 | 1892 | 104 | 1781 | 1,3-beta-glucan synthase component FKS1 OS=Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) OX=235443 GN=FKS1 PE=3 SV=3 |
|
0.0 | 171 | 1927 | 103 | 1855 | 1,3-beta-glucan synthase component FKS1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) OX=559292 GN=FKS1 PE=1 SV=2 |
Other | SP_Sec_SPI | CS Position |
---|---|---|
1.000067 | 0.000001 |
Start | End |
---|---|
520 | 542 |
555 | 577 |
597 | 616 |
632 | 654 |
689 | 711 |
749 | 771 |
1368 | 1390 |
1423 | 1445 |
1536 | 1558 |
1629 | 1651 |
1671 | 1693 |
1714 | 1736 |
1746 | 1765 |
1777 | 1796 |
1811 | 1833 |
1869 | 1891 |
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