Structural studies of KCTD1 and its disease-causing mutant P20S provide insights into the protein function and misfunction
Pecoraro Giovanni 1Pirone Luciano 2Smaldone Giovanni 1Ruggiero Alessia 2Vitagliano Luigi 2Balasco Nicole 3Pedone Emilia M. 2Berisio Rita 2Coppola Luigi 1Esposito Luciana2
作者信息
- 1. IRCCS SYNLAB SDN
- 2. Institute of Biostructures and Bioimaging, CNR
- 3. Institute of Molecular Biology and Pathology, CNR c/o Department Chemistry, Sapienza University of Rome
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Key words
KCTD proteins/Scalp-Ear-Nipple (SEN) syndrome/human diseases/domain swapping引用本文复制引用
Pecoraro Giovanni,Pirone Luciano,Smaldone Giovanni,Ruggiero Alessia,Vitagliano Luigi,Balasco Nicole,Pedone Emilia M.,Berisio Rita,Coppola Luigi,Esposito Luciana.Structural studies of KCTD1 and its disease-causing mutant P20S provide insights into the protein function and misfunction[EB/OL].(2025-03-28)[2025-12-13].https://www.biorxiv.org/content/10.1101/2024.06.14.599007.学科分类
基础医学/分子生物学/生物化学
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