Reference on EC 2.4.1.142 - chitobiosyldiphosphodolichol beta-mannosyltransferase
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REF. 
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Kaushal, G.P.; Elbein, A.D.
Purification and properties of beta-mannosyltransferase that synthesizes Man-beta-GlcNAc-GlcNAc-pyrophosphoryl-dolichol
Arch. Biochem. Biophys.
250
38-47
1986
Sus scrofa
Kaushal, G.P.; Elbein, A.D.
Partial purification and characterization of beta-mannosyltransferase from suspension-cultured soybean cells
Biochemistry
26
7953-7960
1987
Glycine max
Schwarz, M.; Thiel, C.; Lubbehusen, J.; Dorland, B.; de Koning, T.; von Figura, K.; Lehle, L.; Korner, C.
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik
Am. J. Hum. Genet.
74
472-481
2004
Homo sapiens
Kranz, C.; Denecke, J.; Lehle, L.; Sohlbach, K.; Jeske, S.; Meinhardt, F.; Rossi, R.; Gudowius, S.; Marquardt, T.
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I
Am. J. Hum. Genet.
74
545-551
2004
Homo sapiens (Q9BT22), Homo sapiens
Takahashi, T.; Honda, R.; Nishikawa, Y.
Cloning of the human cDNA which can complement the defect of the yeast mannosyltransferase I-deficient mutant alg 1
Glycobiology
10
321-327
2000
Homo sapiens (Q9BT22), Homo sapiens
Gao, X.D.; Nishikawa, A.; Dean, N.
Physical interactions between the Alg1, Alg2, and Alg11 mannosyltransferases of the endoplasmic reticulum
Glycobiology
14
559-570
2004
Saccharomyces cerevisiae
Grubenmann, C.E.; Frank, C.G.; Huelsmeier, A.J.; Schollen, E.; Matthijs, G.; Mayatepek, E.; Berger, E.G.; Aebi, M.; Hennet, T.
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik
Hum. Mol. Genet.
13
535-542
2004
Homo sapiens
Dupre, T.; Vuillaumier-Barrot, S.; Chantret, I.; Yaye, H.S.; Le Bizec, C.; Afenjar, A.; Altuzarra, C.; Barnerias, C.; Burglen, L.; de Lonlay, P.; Feillet, F.; Napuri, S.; Seta, N.; Moore, S.E.
Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations
J. Med. Genet.
47
729-735
2010
Homo sapiens (Q9BT22)
Takahashi, T.; Nedachi, T.; Etoh, T.; Tachikawa, H.; Gao, X.D.
Identification and characterization of transcriptional control region of the human beta 1,4-mannosyltransferase gene
Cytotechnology
69
417-434
2017
Homo sapiens (Q9BT22), Homo sapiens
Ramirez, A.S.; Boilevin, J.; Lin, C.W.; Ha Gan, B.; Janser, D.; Aebi, M.; Darbre, T.; Reymond, J.L.; Locher, K.P.
Chemo-enzymatic synthesis of lipid-linked GlcNAc2Man5 oligosaccharides using recombinant Alg1, Alg2 and Alg11 proteins
Glycobiology
27
726-733
2017
Saccharomyces cerevisiae (P16661), Saccharomyces cerevisiae ATCC 204508 (P16661)
Xu, X.X.; Li, S.T.; Wang, N.; Kitajima, T.; Yoko-O, T.; Fujita, M.; Nakanishi, H.; Gao, X.D.
Structural and functional analysis of Alg1 beta-1,4 mannosyltransferase reveals the physiological importance of its membrane topology
Glycobiology
28
741-753
2018
Saccharomyces cerevisiae (P16661), Saccharomyces cerevisiae, Saccharomyces cerevisiae ATCC 204508 (P16661)
Kobayashi, M.; Jitoku, D.; Iwayama, Y.; Yamamoto, N.; Toyota, T.; Suzuki, K.; Kikuchi, M.; Hashimoto, T.; Kanahara, N.; Kurumaji, A.; Yoshikawa, T.; Nishikawa, T.
Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population
PLoS ONE
13
e0190991
2018
Rattus norvegicus (D4A5S6), Homo sapiens (Q9BT22), Homo sapiens
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