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Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity

期刊

出版社

MDPI
DOI: 10.3390/ijms21062225

关键词

transglutaminase 2; structure-based drug design; protein structure; peptide mimetic

资金

  1. Basic Science Research Program of the National Research Foundation of Korea (NRF) - Korea government (MSIT) [NRF-2017M3A9D8062960, NRF-2018R1A2B2003635]
  2. Korea Healthcare Technology R&D Project, Ministry of Health & Welfare, Republic of Korea [HI17C0155]

向作者/读者索取更多资源

Human transglutaminase 2 (TGase2) has various functions, including roles in various cellular processes such as apoptosis, development, differentiation, wound healing, and angiogenesis, and is linked to many diseases such as cancer. Although TGase2 has been considered an optimized drug target for the treatment of cancer, fibrosis, and neurodegenerative disorders, it has been difficult to generate TGase2-targeted drugs for clinical use because of the relatively flat and broad active site on TGase2. To design more specific and powerful inhibitors, detailed structural information about TGase2 complexed with various effector and inhibitor molecules is required. In this review, we summarized the current structural studies on TGase2, which will aid in designing drugs that can overcome the aforementioned limitations.

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