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Peroxisome

KEGG ID: hsa04146

中文名称

过氧化物酶体

通路描述

过氧化物酶体是发挥氧化还原信号和脂质稳态关键作用的必需细胞器。它们参与许多至关重要的代谢过程,如脂肪酸氧化、醚脂的生物合成以及自由基解毒。过氧化物酶体的生物发生始于早期过氧化物酶 PEX3、PEX16 和 PEX19,并通过多个步骤进行。膜蛋白的导入需要 PEX19 进行识别、靶向和插入,该过程涉及在 PEX3 处的锚定。细胞质基质中的基质蛋白通过过氧化物酶体靶向信号(PTS)被识别并运输至过氧化物酶体膜上的锚定复合物。过氧化物酶体的缺陷会导致严重的且通常致命的遗传性过氧化物酶体疾病(PD)。PD 通常分为两组:第一组是过氧化物酶体生物发生障碍,包括 Zellweger 综合征;第二组是单个过氧化物酶体酶缺陷。
英文描述
Peroxisomes are essential organelles that play a key role in redox signalling and lipid homeostasis. They contribute to many crucial metabolic processes such as fatty acid oxidation, biosynthesis of ether lipids and free radical detoxification. The biogenesis of peroxisomes starts with the early peroxins PEX3, PEX16 and PEX19 and proceeds via several steps. The import of membrane proteins into peroxisomes needs PEX19 for recognition, targeting and insertion via docking at PEX3. Matrix proteins in the cytosol are recognized by peroxisomal targeting signals (PTS) and transported to the docking complex at the peroxisomal membrane. Peroxisomes' deficiencies lead to severe and often fatal inherited peroxisomal disorders (PD). PDs are usually classified in two groups. The first group is disorders of peroxisome biogenesis which include Zellweger syndrome, and the second group is single peroxisomal enzyme deficiencies.

所含基因

83 个基因