Protein trafficking to the apicoplast: deciphering the apicomplexan solution to secondary endosymbiosis.
作者信息
Parsons Marilyn, Karnataki Anuradha, Feagin Jean E, DeRocher Amy
机构信息
Seattle Biomedical Research Institute, 307 Westlake Ave. North, Seattle, WA 98109, USA.
出版信息
Eukaryot Cell. 2007 Jul;6(7):1081-8. doi: 10.1128/EC.00102-07. Epub 2007 May 18.
Abstract
摘要
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本文引用的文献
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Cell cycle-regulated vesicular trafficking of Toxoplasma APT1, a protein localized to multiple apicoplast membranes.细胞周期调控的弓形虫APT1的囊泡运输，APT1是一种定位于多个质体膜的蛋白质。
Mol Microbiol. 2007 Mar;63(6):1653-68. doi: 10.1111/j.1365-2958.2007.05619.x.
2
Fatty acid biosynthesis as a drug target in apicomplexan parasites.脂肪酸生物合成作为顶复门寄生虫的药物靶点。
Curr Drug Targets. 2007 Jan;8(1):15-30. doi: 10.2174/138945007779315579.
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Isoprenoid biosynthesis of the apicoplast as drug target.以顶质体的类异戊二烯生物合成作为药物靶点。
Curr Drug Targets. 2007 Jan;8(1):3-13. doi: 10.2174/138945007779315551.
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Mol Biol Evol. 2007 Apr;24(4):918-28. doi: 10.1093/molbev/msm008. Epub 2007 Jan 22.
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N-terminal positively charged amino acids, but not their exact position, are important for apicoplast transit peptide fidelity in Toxoplasma gondii.N端带正电荷的氨基酸，而非其确切位置，对刚地弓形虫顶质体转运肽的保真度很重要。
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