ATP7A型
型三磷酸腺脢
ATP酶
铜
门克斯病
转运蛋白
化学
分泌物
生物化学
铜缺乏
细胞生物学
新陈代谢
ATP水解
高尔基体
酶
生物
铜代谢
细胞
有机化学
作者
Małgorzata Lenartowicz,Wojciech Krzeptowski
出处
期刊:PubMed
日期:2010-01-01
卷期号:56 (3): 317-27
被引量:9
摘要
Living organisms have developed refined and geneticaly controlled mechanisms of the copper metabolism and transport. ATP7A and ATP7B proteins play the key role in copper homeostasis in the organism. Both proteins are P-type Cu-transporting ATPases and use the energy of ATP hydrolysis to transfer the copper ions across the cellular membranes. Both proteins are localised in Golgi aparatus and involved in regulation of overall copper status in the body and their function is the export of excess copper from the cells and delivery of copper ions to Cu-dependent enzymes. Moreover in organism Cu-transporting ATPases are involved in absorption of dietary copper, Cu removal with the bile, placental copper transport and its secretion to the milk during lactation. Moreover it is known that Cu-transporting ATPases play a role in generation of anti-cancer drug resistance. Disturbances of ATP7A and ATP7B function caused by mutations lead to severe metabolic diseases Menkes and Wilson diseases, respectively.
科研通智能强力驱动
Strongly Powered by AbleSci AI