Identification, Tissue Distribution, and Molecular Modeling of Novel Human Isoforms of the Key Enzyme in Sialic Acid Synthesis, UDP-GlcNAc 2-Epimerase/ManNAc Kinase-Reference-Cited by-同舟云学术

Identification, Tissue Distribution, and Molecular Modeling of Novel Human Isoforms of the Key Enzyme in Sialic Acid Synthesis, UDP-GlcNAc 2-Epimerase/ManNAc Kinase

Published:2011-09-19 Issue:41 Volume:50 Page:8914-8925
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Yardeni Tal¹²,Choekyi Tsering³,Jacobs Katherine¹,Ciccone Carla¹,Patzel Katherine¹,Anikster Yair²,Gahl William A.¹,Kurochkina Natalya³,Huizing Marjan¹

Affiliation:

1. Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, United States

2. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel

3. The School of Theoretical Modeling, Chevy Chase, Maryland 20825, United States

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi201050u

Reference42 articles.

1. A Bifunctional Enzyme Catalyzes the First Two Steps in N-Acetylneuraminic Acid Biosynthesis of Rat Liver

2. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

3. Advances in the Biology and Chemistry of Sialic Acids

4. Diversity in cell surface sialic acid presentations: implications for biology and disease

5. THE FEEDBACK CONTROL OF SUGAR NUCLEOTIDE BIOSYNTHESIS IN LIVER

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