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

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...

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Detalles Bibliográficos
Autores principales: Kim, Gi Eob, Park, Hyun Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139744/
https://www.ncbi.nlm.nih.gov/pubmed/32210142
http://dx.doi.org/10.3390/ijms21062225
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author Kim, Gi Eob
Park, Hyun Ho
author_facet Kim, Gi Eob
Park, Hyun Ho
author_sort Kim, Gi Eob
collection PubMed
description 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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spelling pubmed-71397442020-04-10 Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity Kim, Gi Eob Park, Hyun Ho Int J Mol Sci Review 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. MDPI 2020-03-23 /pmc/articles/PMC7139744/ /pubmed/32210142 http://dx.doi.org/10.3390/ijms21062225 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kim, Gi Eob
Park, Hyun Ho
Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity
title Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity
title_full Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity
title_fullStr Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity
title_full_unstemmed Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity
title_short Structures of Human Transglutaminase 2: Finding Clues for Interference in Cross-linking Mediated Activity
title_sort structures of human transglutaminase 2: finding clues for interference in cross-linking mediated activity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139744/
https://www.ncbi.nlm.nih.gov/pubmed/32210142
http://dx.doi.org/10.3390/ijms21062225
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