نتایج جستجو برای: mannose 1 phosphate guanyltransferas

تعداد نتایج: 2826486  

Journal: :Chemical communications 2003
Céline Pérollier Samuel Constant Jonathan J Jodry Gérald Bernardinelli Jérôme Lacour

Mannose derived hexacoordinated phosphate--prepared in two steps from methyl-alpha-D-mannopyranoside--is a chiral anionic auxiliary with broad asymmetric efficiency.

Journal: :Journal of proteome research 2008
David E Sleat Maria Cecilia Della Valle Haiyan Zheng Dirk F Moore Peter Lobel

Most luminal lysosomal proteins are synthesized as precursors containing mannose 6-phosphate (Man6-P) and a number of recent studies have conducted affinity purification of Man6-P containing proteins as a step toward defining the composition of the lysosome. Approximately 60 known lysosomal proteins have been found in such studies as well as many other Man-6-P glycoproteins, some of which repre...

Journal: :The Biochemical journal 1977
C T Brett L F Leloir

A glucose acceptor was isolated from soya beans by extraction with chloroform/methanol (2:1, v/v), followed by DEAE-cellulose column chromatography of the extract. This acceptor could not be distinguished from liver dolichyl monophosphate by t.l.c. It could replace dolichyl monophosphate as a mannose acceptor with a liver enzyme and its glucosylated derivative could replace dolichyl monophospha...

Journal: :American journal of physiology. Endocrinology and metabolism 2005
T Taguchi E Yamashita T Mizutani H Nakajima M Yabuuchi N Asano I Miwa

D-mannose is an essential monosaccharide constituent of glycoproteins and glycolipids. However, it is unknown how plasma mannose is supplied. The aim of this study was to explore the source of plasma mannose. Oral administration of glucose resulted in a significant decrease of plasma mannose concentration after 20 min in fasted normal rats. However, in fasted type 2 diabetes model rats, plasma ...

2013
Jaime Chu Alexander Mir Ningguo Gao Sabrina Rosa Christopher Monson Vandana Sharma Richard Steet Hudson H. Freeze Mark A. Lehrman Kirsten C. Sadler

Individuals with congenital disorders of glycosylation (CDG) have recessive mutations in genes required for protein N-glycosylation, resulting in multi-systemic disease. Despite the well-characterized biochemical consequences in these individuals, the underlying cellular defects that contribute to CDG are not well understood. Synthesis of the lipid-linked oligosaccharide (LLO), which serves as ...

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