P-POD: Princeton Protein Orthology Database: GO3/Para1408

This family has 11 members: 1 Arabidopsis thaliana, 1 Caenorhabditis elegans, 1 Danio rerio, 1 Dictyostelium discoideum, 1 Drosophila melanogaster, 1 Gallus gallus, 1 Homo sapiens, 1 Mus musculus, 1 Rattus norvegicus, 1 Saccharomyces cerevisiae, 1 Schizosaccharomyces pombe.

Interactive Java Applets: Notung Tree Analysis · Jalview Alignment

GO3/Para1408
11 members.
OrganismProtein (Synonyms)DescriptionAmiGO
A. thalianaTAIR:locus:2042411 (F16B22.15 · AT2G44660) · NCBI:NP_181994.2⌘
C. elegansWB:WBGene00007464 (C08H9.3) · UniProtKB:P52887⌘
D. rerioUniProtKB:Q6ZM97 · ZFIN:ZDB-GENE-030131-5812 (alg8)asparagine-linked glycosylation 8 homolog (yeast, alpha-1,3-glucosyltransferase)⌘
D. discoideumUniProtKB:Q554E2 · dictyBase:DDB_G0275261 (alg8)dolichyl-phosphate-glucose alpha-1,3-glucosyltransferase, glycosyltransferase⌘
D. melanogasterFB:FBgn0029906 (CG4542) · UniProtKB:Q9W3V8⌘
G. gallusNCBI:XP_425656 · ENTREZ:428097
H. sapiensENSEMBL:ENSG00000159063 · UniProtKB:Q9BVK2 (IPI00032370 · HUSSY-02 · ALG8 · Q9BVK2 · ALG8_HUMAN)Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase⌘
M. musculusUniProtKB:Q6P8H8 · MGI:MGI:2141959 (LOC381903 · Alg8)asparagine-linked glycosylation 8 homolog (yeast, alpha-1,3-glucosyltransferase)⌘
R. norvegicusUniProtKB:Q497D1 · RGD:1305468 (Alg8)asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog (S. cerevisiae)⌘
S. cerevisiaeUniProtKB:P40351 · SGD:S000005593 (YOR067C · ALG8 · YOR29-18)Glucosyl transferase, involved in N-linked glycosylation⌘
S. pombeUniProtKB:Q10479 · GeneDB_Spombe:SPAC17C9.07 (alg8 · SPAC17C9.07)glucosyltransferase Alg8⌘
ProteinPublicationCurator Notes
UniProtKB:P40351 · SGD:S000005593PMID:15235028 Schollen E, et al. Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). J Med Genet. 2004 Jul;41(7):550-6.The H. sapiens protein Q9BVK2 complements a homologous mutation in S. cerevisiae. Human ALG8 cmplements a yeast alg8 deletion in a wbp1-1 background.
DescriptionSuffix
Sequences in this family.fasta
mafft aligned Fasta file.afasta
phyml newick file.newick
Notung rooted & rearranged newick file.newick.rooting.0.rearrange.0
Notung Homolog Table.newick.rooting.0.rearrange.0.homologs.csv
OMIM (1)
UniProtKB:P40351 · SGD:S000005593#608104 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H;;CDG Ih; CDGIh
SGD Disease Papers (1)
UniProtKB:P40351 · SGD:S000005593PMID:15235028 Schollen E, et al. (2004) Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). J Med Genet 41(7):550-6
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