Author

J. A. Manso

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2 Biophysics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:bacteria (other)· 1 Organism:C. elegans· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Carabias· 2 shared J. M. de Pereda· 2 shared S. Macedo-Ribeiro· 2 shared A. Sonnenberg· 1 shared D. Nunes-Costa· 1 shared I. Garcia-Rubio· 1 shared M. Gomez-Hernandez· 1 shared M. Kreft· 1 shared

Activity by Year

2018-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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2 shared papersBiochemistry

A. Carabias

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BiochemistrybioRxivAug 23, 2022

Pathogen-specific structural features of two key players in Candida albicans morphogenetic switch

J. A. Manso, A. Carabias, Z. Sarkany…·S. Macedo-Ribeiro

This study identifies unique structural features of CaRas1 and its activation by CaCdc25 in Candida albicans, revealing potential targets for antifungal therapies.

DOI 10.1128/mbio.00638-23

C. elegansstructural biology

𝕏 PostBluesky

BiophysicsbioRxivDec 20, 2018

Integrin α6β4 recognition of a linear motif of bullous pemphigoid antigen BP230 controls its recruitment to hemidesmosomes

J. A. Manso, M. Gomez-Hernandez, A. Carabias…·J. M. de Pereda

The paper identifies a linear motif in BP230 that binds to integrin β4, essential for hemidesmosome assembly, and shows that disrupting this interaction prevents BP230 recruitment.

DOI 10.1016/j.str.2019.03.016

humanexperimental assay

𝕏 PostBluesky

BiochemistrybioRxivNov 29, 2018

Molecular fingerprints for a novel glucosamine kinase family in Actinobacteria

J. A. Manso, D. Nunes-Costa, S. Macedo-Ribeiro…·P. J. Pereira

The paper identifies a novel glucosamine kinase family in Actinobacteria through structural and biochemical analysis, revealing a specific binding motif and potential role in antibiotic biosynthesis.

DOI 10.1128/mbio.00239-19

bacteria (other)proteomics

𝕏 PostBluesky