蛋白质/抗原/多肽 >> 重组蛋白
重组12号染色体开放阅读框72蛋白
半岛bd体育手机客户端 介绍
基因名:
ETFBKMT 半岛bd体育手机客户端 别名: C12orf72; ETFB-KMT; METTL20; ETFBKMT; electron transfer flavoprotein subunit beta lysine methyltransferase; electron transfer flavoprotein subunit beta lysine methyltransferase; electron transfer flavoprotein beta subunit lysine methyltransferase; ETFB lysine methyltransferase; methyltransferase like 20; methyltransferase-like protein 20; protein N-lysine methyltransferase METTL20; 12号染色体开放阅读框72; 背景信息:
GTPase-activating proteins (GAPs) accelerate the intrinsic rate of GTP hydrolysis of Ras-related proteins, resulting in downregulation of their active form. ARHGAP36 (Rho GTPase activating protein 36) is a 547 amino acid protein that contains one Rho-GAP domain. Conserved in chimpanzee, dog, cow, mouse and rat, ARHGAP36 exists as five alternatively spliced isoforms and is encoded by a gene that maps to human chromosome Xq26.1. Chromosome X consists of nearly 153 million base pairs encoding approximately 1,000 genes. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are X chromosome-linked conditions that affect males more frequently because males carry a single X chromosome.
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