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Hexa-Longin domain scaffolds for inter-Rab signalling

SUMMARY: CPLANE is a protein complex required for assembly and maintenance of primary cilia. It contains several proteins, such as INTU, FUZ, WDPCP, JBTS17 and RSG1 (REM2- and RAB-like small GTPase 1), whose genes are mutated in ciliopathies. Using two contrasting evolutionary analyses, coevolution-...

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Detalles Bibliográficos
Autores principales: Sanchez-Pulido, Luis, Ponting, Chris P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703760/
https://www.ncbi.nlm.nih.gov/pubmed/31562761
http://dx.doi.org/10.1093/bioinformatics/btz739
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author Sanchez-Pulido, Luis
Ponting, Chris P
author_facet Sanchez-Pulido, Luis
Ponting, Chris P
author_sort Sanchez-Pulido, Luis
collection PubMed
description SUMMARY: CPLANE is a protein complex required for assembly and maintenance of primary cilia. It contains several proteins, such as INTU, FUZ, WDPCP, JBTS17 and RSG1 (REM2- and RAB-like small GTPase 1), whose genes are mutated in ciliopathies. Using two contrasting evolutionary analyses, coevolution-based contact prediction and sequence conservation, we first identified the INTU/FUZ heterodimer as a novel member of homologous HerMon (Hermansky-Pudlak syndrome and MON1-CCZ1) complexes. Subsequently, we identified homologous Longin domains that are triplicated in each of these six proteins (MON1A, CCZ1, HPS1, HPS4, INTU and FUZ). HerMon complexes are known to be Rab effectors and Rab GEFs (Guanine nucleotide Exchange Factors) that regulate vesicular trafficking. Consequently, INTU/FUZ, their homologous complex, is likely to act as a GEF during activation of Rab GTPases involved in ciliogenesis. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-77037602020-12-07 Hexa-Longin domain scaffolds for inter-Rab signalling Sanchez-Pulido, Luis Ponting, Chris P Bioinformatics Discovery Notes SUMMARY: CPLANE is a protein complex required for assembly and maintenance of primary cilia. It contains several proteins, such as INTU, FUZ, WDPCP, JBTS17 and RSG1 (REM2- and RAB-like small GTPase 1), whose genes are mutated in ciliopathies. Using two contrasting evolutionary analyses, coevolution-based contact prediction and sequence conservation, we first identified the INTU/FUZ heterodimer as a novel member of homologous HerMon (Hermansky-Pudlak syndrome and MON1-CCZ1) complexes. Subsequently, we identified homologous Longin domains that are triplicated in each of these six proteins (MON1A, CCZ1, HPS1, HPS4, INTU and FUZ). HerMon complexes are known to be Rab effectors and Rab GEFs (Guanine nucleotide Exchange Factors) that regulate vesicular trafficking. Consequently, INTU/FUZ, their homologous complex, is likely to act as a GEF during activation of Rab GTPases involved in ciliogenesis. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2020-02-15 2019-09-28 /pmc/articles/PMC7703760/ /pubmed/31562761 http://dx.doi.org/10.1093/bioinformatics/btz739 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Discovery Notes
Sanchez-Pulido, Luis
Ponting, Chris P
Hexa-Longin domain scaffolds for inter-Rab signalling
title Hexa-Longin domain scaffolds for inter-Rab signalling
title_full Hexa-Longin domain scaffolds for inter-Rab signalling
title_fullStr Hexa-Longin domain scaffolds for inter-Rab signalling
title_full_unstemmed Hexa-Longin domain scaffolds for inter-Rab signalling
title_short Hexa-Longin domain scaffolds for inter-Rab signalling
title_sort hexa-longin domain scaffolds for inter-rab signalling
topic Discovery Notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703760/
https://www.ncbi.nlm.nih.gov/pubmed/31562761
http://dx.doi.org/10.1093/bioinformatics/btz739
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