Secondary structure and 1H, 15 N & 13C resonance assignments of the periplasmic domain of OutG, major pseudopilin from Dickeya dadantii type II secretion system

Autor: Theis Jacobsen, Régine Dazzoni, Melvin G. Renault, Benjamin Bardiaux, Michael Nilges, Vladimir Shevchik, Nadia Izadi-Pruneyre

Publikováno v: Biomolecular NMR Assignments
Biomolecular NMR Assignments, 2022, 16 (2), pp.231-236. ⟨10.1007/s12104-022-10085-4⟩
Biomol NMR Assign

The ability to interact and adapt to the surrounding environment is vital for bacteria that colonise various niches and organisms. One strategy developed by Gram-negative bacteria is to secrete exoprotein substrates via the type II secretion system (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867027f71b3eb1944b9104c37687db36
https://hal.science/hal-03836613/document

The Extended 'Two-Barrel' Polymerases Superfamily: Structure, Function and Evolution

Autor: Ludovic Sauguet

Publikováno v: Journal of Molecular Biology
Journal of Molecular Biology, 2019, 431 (20), pp.4167-4183. ⟨10.1016/j.jmb.2019.05.017⟩
Journal of Molecular Biology, Elsevier, 2019, 431 (20), pp.4167-4183. ⟨10.1016/j.jmb.2019.05.017⟩

International audience; DNA and RNA polymerases (DNAP and RNAP) play central roles in genome replication, maintenance and repair, as well as in the expression of genes through their transcription. Multisubunit RNAPs carry out transcription and are re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f44f349829aad5f44e2f739054e021e
https://hal-pasteur.archives-ouvertes.fr/pasteur-02888332/file/S0022283619302864.pdf

Molecular Landscape of the Ribosome Pre-initiation Complex during mRNA Scanning: Structural Role for eIF3c and Its Control by eIF5

Autor: Asokan Ananbandam, Hisashi Yoshida, Florian Stengel, Mahmoud L. Nasr, Brytteny Thompson, Takeshi Urano, Fan Zhang, Philip Gao, Haribabu Arthanari, Takashi Nagata, Riccardo Pellarin, Gerhard Wagner, Alan G. Hinnebusch, Jacob Morris, Rafael E. Luna, Katsura Asano, Evangelos Papadopoulos, Chelsea Moore, Eric Aube, Pilar Martin-Marcos, Hiroyuki Hiraishi, Eiji Obayashi, Eddie Dagraca, Jan P. Erzberger, Chingakham Ranjit Singh, Satoru Unzai, Ian Harmon, Samantha Hustak

Publikováno v: Cell Reports
Cell Reports, 2017, 18 (11), pp.2651-2663. ⟨10.1016/j.celrep.2017.02.052⟩
Cell Reports, Elsevier Inc, 2017, 18 (11), pp.2651-2663. ⟨10.1016/j.celrep.2017.02.052⟩
Cell Reports, 18 (11)
Cell Reports, Vol 18, Iss 11, Pp 2651-2663 (2017)

During eukaryotic translation initiation, eIF3 binds the solvent-accessible side of the 40S ribosome and recruits the gate-keeper protein eIF1 and eIF5 to the decoding center. This is largely mediated by the N-terminal domain (NTD) of eIF3c, which ca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e94474aec1da25a265c0c4cdc5072f39
https://doi.org/10.1016/j.celrep.2017.02.052

Mutations in the BAF-complex subunit DPF2 associated with Coffin-Siris syndrome

Autor: Andrew O.M. Wilkie, Georgia Vasileiou, Bernt Popp, Yun Li, Maren Wenzel, Marion Gérard, Susan Tomkins, Jenny Morton, Megan T. Cho, André Reis, Astrid Weber, George E. Hoganson, Beate Albrecht, Felix B. Engel, Arif B. Ekici, Maria-Renée Plona, Janine Altmüller, Christian Thiel, Christian Büttner, Jill Clayton-Smith, Karen Low, Dagmar Wieczorek, Deciphering Developmental Disorders Study, Bernd Wollnik, Eduardo Calpena, Nuria C. Bramswig, Sabine Endele, Hermann-Josef Lüdecke, Silvia Vergarajauregui, Tim M. Strom

Publikováno v: The American Journal of Human Genetics
The American Journal of Human Genetics, 2018, 102 (3), pp.468-479. ⟨10.1016/j.ajhg.2018.01.014⟩
Am. J. Hum. Genet. 102, 468-479 (2018)
Publons
Web of Science
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2018, 102 (3), pp.468-479. ⟨10.1016/j.ajhg.2018.01.014⟩
Vasileiou, G, Vergarajauregui, S, Endele, S, Popp, B, Büttner, C, Ekici, A B, Gerard, M, Bramswig, N C, Albrecht, B, Clayton-Smith, J, Morton, J, Tomkins, S, Low, K, Weber, A, Wenzel, M, Altmüller, J, Li, Y, Wollnik, B, Hoganson, G, Plona, M R, Cho, M T, Thiel, C T, Lüdecke, H J, Strom, T M, Calpena, E, Wilkie, A O M, Wieczorek, D, Engel, F B, Reis, A & Deciphering Developmental Disorders Study 2018, ' Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome ', American Journal of Human Genetics, vol. 102, no. 3, pp. 468-479 . https://doi.org/10.1016/j.ajhg.2018.01.014

International audience; Variants affecting the function of different subunits of the BAF chromatin-remodelling complex lead to various neurodevelopmental syndromes, including Coffin-Siris syndrome. Furthermore, variants in proteins containing PHD fin

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https://ora.ox.ac.uk/objects/uuid:fa6f808e-e7d1-48e4-a62a-f6c7526d4553

Dysregulation of chromatin remodelling complexes in amyotrophic lateral sclerosis

Autor: Ekaterina Rogaeva, Julia Keith, Janice Robertson, Heather D. Durham, Benoit J. Gentil, Christine Marques, Beibei Zhao, Caroline Rouaux, Lorne Zinman, Sandra Minotti, Michael Tibshirani

Publikováno v: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2017, 26 (21), pp.4142-4152. ⟨10.1093/hmg/ddx301⟩
Human Molecular Genetics, 2017, 26 (21), pp.4142-4152. ⟨10.1093/hmg/ddx301⟩

International audience; Amyotrophic lateral sclerosis is a fatal neurodegenerative disease with paralysis resulting from dysfunction and loss of motor neurons. A common neuropathological finding is attrition of motor neuron dendrites, which make cent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131ff34cb0fcb1cd5c047a64d916b0e8
https://www.hal.inserm.fr/inserm-03375235/document