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参与HNK-1碳水化合物表位生物合成的人葡萄糖醛酸基转移酶的克隆与染色体定位。

Cloning and chromosomal mapping of human glucuronyltransferase involved in biosynthesis of the HNK-1 carbohydrate epitope.

作者信息

Mitsumoto Y, Oka S, Sakuma H, Inazawa J, Kawasaki T

机构信息

Department of Biological Chemistry and CREST (Core Research for Educational Science and Technology) Project, Japan Science and Technology Corporation, Kyoto, 606-8501, Japan.

出版信息

Genomics. 2000 Apr 15;65(2):166-73. doi: 10.1006/geno.2000.6152.

Abstract

The HNK-1 carbohydrate is expressed on various cell adhesion molecules in the nervous system and is suggested to play a role in cell-cell and cell-substrate interactions. Here we describe the isolation of a cDNA encoding human glucuronyltransferase (GlcAT-P), which is a key enzyme in the biosynthesis of the HNK-1 carbohydrate. The primary structure deduced from the cDNA sequence predicted a type II transmembrane protein of 334 amino acids. Human GlcAT-P was 98.2% identical with rat GlcAT-P in amino acid sequence, the exception being the length of the cytoplasmic tail. Northern blot analysis indicated that human GlcAT-P is expressed mainly in the brain. There is a single copy of the human GlcAT-P gene (HGMW-approved symbol B3GAT1), and it was mapped to chromosome 11q25.

摘要

HNK-1碳水化合物在神经系统的多种细胞黏附分子上表达,并被认为在细胞间和细胞与底物的相互作用中发挥作用。在此,我们描述了一种编码人葡糖醛酸基转移酶(GlcAT-P)的cDNA的分离,该酶是HNK-1碳水化合物生物合成中的关键酶。从cDNA序列推导的一级结构预测为一个334个氨基酸的II型跨膜蛋白。人GlcAT-P与大鼠GlcAT-P的氨基酸序列有98.2%的同一性,不同之处在于细胞质尾巴的长度。Northern印迹分析表明人GlcAT-P主要在脑中表达。人GlcAT-P基因有一个单拷贝(HGMW批准符号为B3GAT1),并被定位到11号染色体q25区。

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