@prefix dcat: <http://www.w3.org/ns/dcat#> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix foaf: <http://xmlns.com/foaf/0.1/> .
@prefix vcard: <http://www.w3.org/2006/vcard/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

<https://rec.harvest-normandie.data4citizen.com/dataset/oai-hal-tel-00839505v1> a dcat:Dataset ;
    dct:description """
              The hijacking of cellular machinery by pathogens, is essential to spread through the body of the host. Perturbation of signaling pathways that control cell homeostasis is a strategy developed by many other viruses upon infection. One originality of rabies virus is that it induces survival of infected neurons to ensure its propagation. The PDZ binding site (PDZ-BS) of the glycoprotein of rabies virus was identified as a key element to control survival and apoptosis pathways. The PDZ-BS of the glycoprotein from the virulent strain recognizes only two isoforms of the Microtubule Associated Serine/Threonine kinase family (MAST1 and MAST2). MAST2 acts as a survival inhibitor that stimulates neurite retraction and inhibits their elongation. In addition MAST2 interacts with the PDZ-BS of the phosphatase PTEN that is another inhibitor of neuronal survival. We propose that the glycoprotein disrupts the PTEN/MAST2 complex by competition with the PDZ-BS of PTEN and disturbs cellular homeostasis. The structure of the PDZ domain of MAST2 complexed with its endogenous ligand (PTEN13-Cter) reveals an original interaction with a large surface of interaction. This interaction network is preserved in MAST2 PDZ domain complexed with the viral ligand (Cyto13-vir). We demonstrated that the PDZ-BS of the glycoprotein is essential to trigger neuronal survival and that it induces a partial exclusion of PTEN from the nucleus. It is well established that the phosphorylation of PTEN is controlled by its phosphorylation state
            """ ;
    dct:identifier "NNT: 2012PAO66292" ;
    dct:issued "2026-05-10T13:00:06.855808"^^xsd:dateTime ;
    dct:language "fr" ;
    dct:modified "2026-05-10T13:00:06.855814"^^xsd:dateTime ;
    dct:publisher <https://rec.harvest-normandie.data4citizen.com/organization/cce9db95-46d9-4dc2-84b6-764215d0a002> ;
    dct:title "MAST 2 involvement in the mechanism of neuronal survival pathways induced by the rabies glycoprotein" ;
    dcat:contactPoint [ a vcard:Organization ;
            vcard:fn "CCSD" ] ;
    dcat:distribution <https://rec.harvest-normandie.data4citizen.com/dataset/oai-hal-tel-00839505v1/resource/4bf6f0db-e45d-461c-9586-de2d74ddc240> ;
    dcat:keyword "domaine-pdz",
        "infoeu-reposemanticsdoctoralthesis",
        "kinase",
        "mast2",
        "pten",
        "sdvbbmbplife-sciences-q-biobiochemistry-molecular-biologybiophysics",
        "survie-neuronale",
        "theses",
        "virus-de-la-rage" ;
    dcat:landingPage <https://theses.hal.science/tel-00839505> .

<https://rec.harvest-normandie.data4citizen.com/dataset/oai-hal-tel-00839505v1/resource/4bf6f0db-e45d-461c-9586-de2d74ddc240> a dcat:Distribution ;
    dct:format "HTML" ;
    dct:issued "2026-05-10T13:00:06.858405"^^xsd:dateTime ;
    dct:modified "2026-05-10T13:00:06.838902"^^xsd:dateTime ;
    dct:title "MAST 2 involvement in the mechanism of neuronal survival pathways induced by the rabies glycoprotein" ;
    dcat:accessURL <https://theses.hal.science/tel-00839505> .

<https://rec.harvest-normandie.data4citizen.com/organization/cce9db95-46d9-4dc2-84b6-764215d0a002> a foaf:Agent ;
    foaf:name "test_moissonnage_selune" .

<https://theses.hal.science/tel-00839505> a foaf:Document .

