Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action (V体育安卓版)
- PMID: 12150926
- DOI: 10.1016/s0092-8674(02)00833-4
Raptor, a binding partner of target of rapamycin (TOR), mediates TOR action
Abstract
mTOR controls cell growth, in part by regulating p70 S6 kinase alpha (p70alpha) and eukaryotic initiation factor 4E binding protein 1 (4EBP1). Raptor is a 150 kDa mTOR binding protein that also binds 4EBP1 and p70alpha. The binding of raptor to mTOR is necessary for the mTOR-catalyzed phosphorylation of 4EBP1 in vitro, and it strongly enhances the mTOR kinase activity toward p70alpha. Rapamycin or amino acid withdrawal increases, whereas insulin strongly inhibits, the recovery of 4EBP1 and raptor on 7-methyl-GTP Sepharose. Partial inhibition of raptor expression by RNA interference (RNAi) reduces mTOR-catalyzed 4EBP1 phosphorylation in vitro. RNAi of C. elegans raptor yields an array of phenotypes that closely resemble those produced by inactivation of Ce-TOR. Thus, raptor is an essential scaffold for the mTOR-catalyzed phosphorylation of 4EBP1 and mediates TOR action in vivo VSports手机版. .
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- V体育平台登录 - Actions
- Actions (VSports注册入口)
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- "V体育官网入口" Actions
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- "V体育官网" Actions
- Actions (VSports最新版本)
- Actions (V体育官网入口)
- V体育安卓版 - Actions
- V体育官网入口 - Actions
- Actions (V体育官网)
- V体育安卓版 - Actions
- Actions (VSports在线直播)
- "V体育ios版" Actions
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- "V体育官网" Actions
- Actions (V体育官网)
- "VSports" Actions
- V体育平台登录 - Actions
- V体育官网入口 - Actions
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