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Determining the molecular drivers of species-specific interferon-stimulated gene product 15 interactions with nairovirus ovarian tumor domain proteases

机译：测定特异性特异性干扰素刺激基因产物的分子驱动器15与奈良病毒卵巢肿瘤域蛋白酶的相互作用

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期刊名称 PLoS ONE
作者
John V. Dzimianski; Florine E. M. Scholte; Isabelle L. Williams; Caroline Langley; Brendan T. Freitas; Jessica R. Spengler; Éric Bergeron; Scott D. Pegan;
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作者单位

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年(卷),期 2019(14),12
年度 2019
页码 e0226415
总页数 26
原文格式 PDF
正文语种
中图分类生物学;
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1. Determining the molecular drivers of species-specific interferon-stimulated gene product 15 interactions with nairovirus ovarian tumor domain proteases [J] . John V. Dzimianski, Florine E. M. Scholte, Isabelle L. Williams, PLoS One . 2019,第12期

机译：确定特异性特异性干扰素刺激基因产物的分子驱动器15与奈病毒卵巢肿瘤域蛋白酶的相互作用
2. Structural basis for the removal of ubiquitin and interferon-stimulated gene 15 by a viral ovarian tumor domain-containing protease [J] . Terrence W. James, Natalia Frias-Staheli, John-Paul Bacik, Proceedings of the National Academy of Sciences of the United States of America . 2011,第6期

机译：含病毒性卵巢肿瘤结构域蛋白酶去除泛素和干扰素刺激基因15的结构基础
3. Probing the impact of nairovirus genomic diversity on viral ovarian tumor domain protease (vOTU) structure and deubiquitinase activity [J] . John V. Dzimianski, Brianna S. Beldon, Courtney M. Daczkowski, PLoS Pathogens . 2019,第1期

机译：探索内罗病毒基因组多样性对病毒性卵巢肿瘤结构域蛋白酶（vOTU）结构和去泛素酶活性的影响
4. Bio-molecular optimized interactions and conformational switches in human ERβ and SRC-1 protein: An in silico approach to suppress tumor in breast cancer malignancies: Computational insight for suppression of tumorigenesis in breast malignancies [C] . Arundhati Banerjee, Sujay Ray 2016 International Conference on Microelectronics, Computing and Communications . 2016

机译：人类ERβ和SRC-1蛋白中生物分子的优化相互作用和构象转换：抑制乳腺癌恶性肿瘤的计算机方法：抑制乳腺癌恶性肿瘤发生的计算机洞察
5. The molecular interactions of the catalytic domain of factor XIa (FXIa): Catalysis of substrates IX and S-2366, inhibition by the Kunitz protease inhibitory domain (KPI) of Protease Nexin 2 (PN2), and binding to the surface of activated platelets. [D] . Miller, Tara N. 2007

机译：因子XIa（FXIa）催化域的分子相互作用：底物IX和S-2366的催化，蛋白酶Nexin 2（PN2）的Kunitz蛋白酶抑制域（KPI）的抑制以及与活化血小板表面的结合。
6. Structural basis for the removal of ubiquitin and interferon-stimulated gene 15 by a viral ovarian tumor domain-containing protease [O] . Terrence W. James, Natalia Frias-Staheli, John-Paul Bacik, 2011

机译：含病毒性卵巢肿瘤结构域蛋白酶去除泛素和干扰素刺激基因15的结构基础
7. Determining the molecular drivers of species-specific interferon-stimulated gene product 15 interactions with nairovirus ovarian tumor domain proteases [O] . John V. Dzimianski, Florine E. M. Scholte, Isabelle L. Williams, 2019

机译：测定特异性特异性干扰素刺激基因产物的分子驱动器15与奈良病毒卵巢肿瘤域蛋白酶的相互作用
8. Pathogenesis of Ovarian Serous Carcinoma as the Basis for Immunologic Directed Diagnosis and Treatment. Project 1 - Molecular Characterization of Ovarian Serous Tumors Developing Along Different Pathways [R] . Kurman, R. J. , Shih, I. 2003

机译：卵巢浆液性癌的发病机制是免疫定向诊断和治疗的基础。项目1 - 沿不同途径发展的卵巢浆液性肿瘤的分子特征

Determining the molecular drivers of species-specific interferon-stimulated gene product 15 interactions with nairovirus ovarian tumor domain proteases

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