人 PACS1 抗体对
01AB02238
Phosphofurin acidic cluster sorting protein 1 (PACS1) is a protein-coding gene involved in the localization of trans-Golgi network (TGN) membrane proteins and controls endosome-to-Golgi trafficking. PACS1 binds to phosphorylated acidic cluster motifs on client proteins such as furin and mannose-6-phosphate receptor, mediating their proper sorting and localization within the cell. It interacts with clathrin adaptor complexes like AP-1 and AP-3, playing a crucial role in intracellular trafficking and membrane protein localization. PACS1 also contributes to immune evasion by HIV-1, redirecting MHC-I molecules to the TGN to reduce their surface expression. Pathogenic variants in PACS1 cause multisystemic syndromes characterized by intellectual disability, developmental delays, and craniofacial abnormalities. The gene encodes a 963-amino acid protein essential for normal development, including lymphocyte function. The PACS1 protein contains functional domains such as a furin-binding region and an autoregulatory domain phosphorylated by casein kinase 2, regulating its interactions.
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技术参数
- 靶点基因名
- PACS1
- 基因别名
- KIAA1175
- 蛋白别名
- phosphofurin acidic cluster sorting protein 1; PACS1
- UniProt
- Q6VY07
- 物种
- Human
产品详情
- 靶点名称
- PACS1
- 蛋白名称
- phosphofurin acidic cluster sorting protein 1
- 蛋白别名
- Phosphofurin acidic cluster sorting protein 1; PACS-1
- 靶点基因名
- PACS1
- 基因别名
- KIAA1175
- UniProt
- Q6VY07
- 来源物种
- Homo sapiens (Human)
- 物种反应性
- Human
背景介绍
Phosphofurin acidic cluster sorting protein 1 (PACS1) is a protein-coding gene involved in the localization of trans-Golgi network (TGN) membrane proteins and controls endosome-to-Golgi trafficking. PACS1 binds to phosphorylated acidic cluster motifs on client proteins such as furin and mannose-6-phosphate receptor, mediating their proper sorting and localization within the cell. It interacts with clathrin adaptor complexes like AP-1 and AP-3, playing a crucial role in intracellular trafficking and membrane protein localization. PACS1 also contributes to immune evasion by HIV-1, redirecting MHC-I molecules to the TGN to reduce their surface expression. Pathogenic variants in PACS1 cause multisystemic syndromes characterized by intellectual disability, developmental delays, and craniofacial abnormalities. The gene encodes a 963-amino acid protein essential for normal development, including lymphocyte function. The PACS1 protein contains functional domains such as a furin-binding region and an autoregulatory domain phosphorylated by casein kinase 2, regulating its interactions.