Palde相关文献与解析，生知库 | 链接生命科学的每一步

Kevin Ryan, Ben Bolaňos, Marissa Smith, Prakash B Palde, Paulina Delgado Cuenca, Todd L VanArsdale, Sherry Niessen, Lianglin Zhang, Douglas Behenna, Martha A Ornelas, Khanh T Tran, Stephen Kaiser, Lawrence Lum, Al Stewart, Ketan S Gajiwala

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Human

发表日期：2021

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Molecular Basis for Redox Activation of Epidermal Growth Factor Receptor Kinase

表皮生长因子受体激酶氧化还原激活的分子基础

期刊:Cell Chemical Biology

影响因子:7.2

doi:10.1016/j.chembiol.2016.05.017

Truong, Thu H; Ung, Peter Man-Un; Palde, Prakash B; Paulsen, Candice E; Schlessinger, Avner; Carroll, Kate S

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发表日期：2016

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First-in-Class Inhibitors of Sulfur Metabolism with Bactericidal Activity against Non-Replicating M. tuberculosis

具有针对非复制型结核分枝杆菌的杀菌活性的首创硫代谢抑制剂

期刊:ACS Chemical Biology

影响因子:3.5

doi:10.1021/acschembio.5b00517

Prakash B Palde, Ashima Bhaskar, Laura E Pedró Rosa, Franck Madoux, Peter Chase, Vinayak Gupta, Timothy Spicer, Louis Scampavia, Amit Singh, Kate S Carroll

代谢

发表日期：2016

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Functional Site Discovery in a Sulfur Metabolism Enzyme by Using Directed Evolution

利用定向进化技术发现硫代谢酶中的功能位点

期刊:Chembiochem

影响因子:2.8

doi:10.1002/cbic.201600264

Paritala, Hanumantharao; Palde, Prakash B; Carroll, Kate S

代谢

发表日期：2016

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A universal entropy-driven mechanism for thioredoxin-target recognition

一种通用的熵驱动机制，用于硫氧还蛋白-靶标识别

期刊:Proceedings of the National Academy of Sciences of the United States of America

影响因子:9.1

doi:10.1073/pnas.1504376112

Palde, Prakash B; Carroll, Kate S

发表日期：2015

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Strategies for recognition of stem-loop RNA structures by synthetic ligands: application to the HIV-1 frameshift stimulatory sequence

合成配体识别茎环 RNA 结构的策略：应用于 HIV-1 移码刺激序列

期刊:Journal of Medicinal Chemistry

影响因子:6.8

doi:10.1021/jm100231t

Prakash B Palde, Leslie O Ofori, Peter C Gareiss, Jaclyn Lerea, Benjamin L Miller

Dynamic combinatorial selection of molecules capable of inhibiting the (CUG) repeat RNA-MBNL1 interaction in vitro: discovery of lead compounds targeting myotonic dystrophy (DM1)

动态组合筛选能够抑制体外 (CUG) 重复 RNA-MBNL1 相互作用的分子：发现靶向强直性肌营养不良症 (DM1) 的先导化合物

期刊:Journal of the American Chemical Society

影响因子:15.6

doi:10.1021/ja804398y

Gareiss, Peter C; Sobczak, Krzysztof; McNaughton, Brian R; Palde, Prakash B; Thornton, Charles A; Miller, Benjamin L

Dissecting the molecular determinants of clinical PARP1 inhibitor selectivity for tankyrase1

剖析临床 PARP1 抑制剂对 tankyrase1 选择性的分子决定因素

Molecular Basis for Redox Activation of Epidermal Growth Factor Receptor Kinase

表皮生长因子受体激酶氧化还原激活的分子基础

First-in-Class Inhibitors of Sulfur Metabolism with Bactericidal Activity against Non-Replicating M. tuberculosis

具有针对非复制型结核分枝杆菌的杀菌活性的首创硫代谢抑制剂

Functional Site Discovery in a Sulfur Metabolism Enzyme by Using Directed Evolution

利用定向进化技术发现硫代谢酶中的功能位点

A universal entropy-driven mechanism for thioredoxin-target recognition

一种通用的熵驱动机制，用于硫氧还蛋白-靶标识别

Strategies for recognition of stem-loop RNA structures by synthetic ligands: application to the HIV-1 frameshift stimulatory sequence

合成配体识别茎环 RNA 结构的策略：应用于 HIV-1 移码刺激序列

Dynamic combinatorial selection of molecules capable of inhibiting the (CUG) repeat RNA-MBNL1 interaction in vitro: discovery of lead compounds targeting myotonic dystrophy (DM1)

动态组合筛选能够抑制体外 (CUG) 重复 RNA-MBNL1 相互作用的分子：发现靶向强直性肌营养不良症 (DM1) 的先导化合物