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通过同源建模确定并验证mTOR激酶结构域的三维结构。

Determination and validation of mTOR kinase-domain 3D structure by homology modeling.

作者信息

Lakhlili Wiame, Chevé Gwénaël, Yasri Abdelaziz, Ibrahimi Azeddine

机构信息

Laboratoire de Biotechnologie (MedBiotech), Faculté de Médecine et de Pharmacie de Rabat, Université Mohammed V de Rabat, Rabat, Morroco.

OriBase Pharma, Cap Gamma, Parc Euromédecine, Montpellier, France.

出版信息

Onco Targets Ther. 2015 Jul 30;8:1923-30. doi: 10.2147/OTT.S84200. eCollection 2015.

Abstract

The AKT/mammalian target of rapamycin (mTOR) pathway is considered as one of the commonly activated and deregulated signaling pathways in human cancer. mTOR is associated with other proteins in two molecular complexes: mTOR complex 1/Raptor and the mTOR complex 2/Rictor. Using the crystal structure of the related lipid kinase PI3Kγ, we built a model of the catalytic region of mTOR. The modeling of the three-dimensional (3D) structure of the mTOR was performed by homology modeling program SWISS-MODEL. The quality and validation of the obtained model were performed using PROCHECK and PROVE softwares. The overall stereochemical property of the protein was assessed by the Ramachandran plot. The model validation was also done by docking of known inhibitors. In this paper, we describe and validate a 3D model for the mTOR catalytic site.

摘要

AKT/雷帕霉素哺乳动物靶蛋白(mTOR)信号通路被认为是人类癌症中常见的激活失调信号通路之一。mTOR与其他蛋白质形成两种分子复合物:mTOR复合物1/ Raptor和mTOR复合物2/ Rictor。利用相关脂质激酶PI3Kγ的晶体结构,我们构建了mTOR催化区域的模型。mTOR三维(3D)结构的建模是通过同源建模程序SWISS-MODEL进行的。使用PROCHECK和PROVE软件对所得模型进行质量评估和验证。通过拉氏图评估蛋白质的整体立体化学性质。模型验证还通过对接已知抑制剂来完成。在本文中,我们描述并验证了mTOR催化位点的3D模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67f8/4525790/61e2e8aae635/ott-8-1923Fig1.jpg

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