ARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases
Armadillo repeat-containing proteins (ARMCs) are widely distributed in eukaryotes and have important influences on cell adhesion, signal transduction, mitochondrial function regulation, tumorigenesis, and other processes. These proteins share a similar domain consisting of tandem repeats approximate...
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Frontiers Media S.A.
2021
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oai:doaj.org-article:61a007c8db1b41afbc49069001dc9f542021-12-01T12:16:40ZARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases2296-889X10.3389/fmolb.2021.791597https://doaj.org/article/61a007c8db1b41afbc49069001dc9f542021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fmolb.2021.791597/fullhttps://doaj.org/toc/2296-889XArmadillo repeat-containing proteins (ARMCs) are widely distributed in eukaryotes and have important influences on cell adhesion, signal transduction, mitochondrial function regulation, tumorigenesis, and other processes. These proteins share a similar domain consisting of tandem repeats approximately 42 amino acids in length, and this domain constitutes a substantial platform for the binding between ARMCs and other proteins. An ARMC subfamily, including ARMC1∼10, ARMC12, and ARMCX1∼6, has received increasing attention. These proteins may have many terminal regions and play a critical role in various diseases. On the one hand, based on their similar central domain of tandem repeats, this ARMC subfamily may function similarly to other ARMCs. On the other hand, the unique domains on their terminals may cause these proteins to have different functions. Here, we focus on the ARMC subfamily (ARMC1∼10, ARMC12, and ARMCX1∼6), which is relatively conserved in vertebrates and highly conserved in mammals, particularly primates. We review the structures, biological functions, evolutions, interactions, and related diseases of the ARMC subfamily, which involve more than 30 diseases and 40 bypasses, including interactions and relationships between more than 100 proteins and signaling molecules. We look forward to obtaining a clearer understanding of the ARMC subfamily to facilitate further in-depth research and treatment of related diseases.Yutao HuangYutao HuangZijian JiangXiangyu GaoXiangyu GaoPeng LuoPeng LuoXiaofan JiangXiaofan JiangFrontiers Media S.A.articleArmadillo repeat-containing proteinARMCstructurebiological functionevolutioninteractionBiology (General)QH301-705.5ENFrontiers in Molecular Biosciences, Vol 8 (2021) |
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Armadillo repeat-containing protein ARMC structure biological function evolution interaction Biology (General) QH301-705.5 |
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Armadillo repeat-containing protein ARMC structure biological function evolution interaction Biology (General) QH301-705.5 Yutao Huang Yutao Huang Zijian Jiang Xiangyu Gao Xiangyu Gao Peng Luo Peng Luo Xiaofan Jiang Xiaofan Jiang ARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases |
description |
Armadillo repeat-containing proteins (ARMCs) are widely distributed in eukaryotes and have important influences on cell adhesion, signal transduction, mitochondrial function regulation, tumorigenesis, and other processes. These proteins share a similar domain consisting of tandem repeats approximately 42 amino acids in length, and this domain constitutes a substantial platform for the binding between ARMCs and other proteins. An ARMC subfamily, including ARMC1∼10, ARMC12, and ARMCX1∼6, has received increasing attention. These proteins may have many terminal regions and play a critical role in various diseases. On the one hand, based on their similar central domain of tandem repeats, this ARMC subfamily may function similarly to other ARMCs. On the other hand, the unique domains on their terminals may cause these proteins to have different functions. Here, we focus on the ARMC subfamily (ARMC1∼10, ARMC12, and ARMCX1∼6), which is relatively conserved in vertebrates and highly conserved in mammals, particularly primates. We review the structures, biological functions, evolutions, interactions, and related diseases of the ARMC subfamily, which involve more than 30 diseases and 40 bypasses, including interactions and relationships between more than 100 proteins and signaling molecules. We look forward to obtaining a clearer understanding of the ARMC subfamily to facilitate further in-depth research and treatment of related diseases. |
format |
article |
author |
Yutao Huang Yutao Huang Zijian Jiang Xiangyu Gao Xiangyu Gao Peng Luo Peng Luo Xiaofan Jiang Xiaofan Jiang |
author_facet |
Yutao Huang Yutao Huang Zijian Jiang Xiangyu Gao Xiangyu Gao Peng Luo Peng Luo Xiaofan Jiang Xiaofan Jiang |
author_sort |
Yutao Huang |
title |
ARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases |
title_short |
ARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases |
title_full |
ARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases |
title_fullStr |
ARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases |
title_full_unstemmed |
ARMC Subfamily: Structures, Functions, Evolutions, Interactions, and Diseases |
title_sort |
armc subfamily: structures, functions, evolutions, interactions, and diseases |
publisher |
Frontiers Media S.A. |
publishDate |
2021 |
url |
https://doaj.org/article/61a007c8db1b41afbc49069001dc9f54 |
work_keys_str_mv |
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