ARC5 | Dynamin-like protein ARC5 供应商 Agrisera 产品货号 AS13-2676 产品报价 ￥询价/50ug 产品说明书 点击查看 购买方式 银行转账、电汇、支票、现金,在线支付宝及网银支付,或直接与我们电话联系400-6800-868。 产品新闻 背景资料 ARC5 (Dynamin-like protein ARC5) is a probable GTPase component of bo...
W. ARC5, a cytosolic dynamin-like protein from plants, is part of the chloroplast division machinery. Proc. Natl Acad. Sci. USA 100, 4328–4333 (2003). Article CAS PubMed PubMed Central Google Scholar Glynn, J. M., Miyagishima, S. Y., Yoder, D. W., Osteryoung, K. W. & ...
Therefore, ARC5 is important but not essential for chloroplast division and it probably evolved to facilitate the division of chloroplasts during endosymbiosis.; FZO is a more diverged dynamin-related protein involved in mitochondrial fusion in metazoa and fungi. However, an FZO-like protein in ...
Dynamin-like proteins are membrane remodeling GTPases with well-understood functions in eukaryotic cells. However, bacterial dynamin-like proteins are still poorly investigated.SynDLP, the dynamin-like protein of the cyanobacteriumSynechocystissp. PCC 6803, forms ordered oligomers in solution. The 3.7...
Dynamin-like protein encoded by the Drosophila shibire gene associated with vesicular traffic Nature, 351 (6325) (1991), pp. 411-414 1674590 10.1038/351411a0 View in ScopusGoogle Scholar 37 M Mettlen, T Pucadyil, R Ramachandran, SL Schmid Dissecting dynamin's role in clathrin-mediated endocyto...
Over the past decade, it has become evident that multiple endocytic pathways operate in eukaryotic cells, and several of these are dependent on dynamins and dynamin-related proteins (DRPs). Many members of the DRP superfamily possess the ability to self-assemble into long spiral polymers that wr...
protein-1 (Drp1), thereby decreasing Drp1 accumulation in mitochondria and Drp1-mediated activation of the mitochondrial fission program. We also found that p53 transcriptionally downregulates miR-499 expression. Our data reveal a role for miR-499 in regulating the mitochondrial fission machinery and ...
Autosomal dominant optic atrophy (ADOA) is the most prevalent hereditary optic neuropathy resulting in progressive loss of visual acuity, centrocoecal scotoma and bilateral temporal atrophy of the optic nerve with an onset within the first two decades of