过氧化物酶体
中文名称
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
ABCD1
ABCD2
ABCD3
ABCD4
ACAA1
ACOT8
ACOX1
ACOX2
ACOX3
ACSL1
ACSL3
ACSL4
ACSL5
ACSL6
AGPS
AGXT
AMACR
BAAT
CAT
CRAT
CROT
DAO
DDO
DECR2
DHRS4
ECH1
ECI2
EHHADH
EPHX2
FAR1
FAR2
GNPAT
GSTK1
HACL1
HAO1
HAO2
HMGCL
HMGCLL1
HSD17B4
IDH1
IDH2
MLYCD
MPV17
MPV17L
MPV17L2
MVK
NOS2
NUDT12
NUDT13
NUDT19
NUDT7
PAOX
PECR
PEX1
PEX10
PEX11A
PEX11B
PEX11G
PEX12
PEX13
PEX14
PEX16
PEX19
PEX2
PEX26
PEX3
PEX5
PEX5L
PEX6
PEX7
PHYH
PIPOX
PMVK
PRDX1
PRDX5
PXMP2
PXMP4
SCP2
SLC25A17
SLC27A2
SOD1
SOD2
XDH