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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Autores principales: Yutao Huang, Zijian Jiang, Xiangyu Gao, Peng Luo, Xiaofan Jiang
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Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/61a007c8db1b41afbc49069001dc9f54
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spelling 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)
institution DOAJ
collection DOAJ
language EN
topic Armadillo repeat-containing protein
ARMC
structure
biological function
evolution
interaction
Biology (General)
QH301-705.5
spellingShingle 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
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