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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7139744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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