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ProteomicsPeptide and MUC5B hydrolysis by the Mucin Degrading Protease (MdpL) from Limosilactobacillus fermentum
MUC5B is the predominant glycoprotein in saliva and is instrumental in the establishment and maintenance of multi-species eubiotic biofilms in the oral cavity. Investigations of the aciduric Lactobacillaceae family, and its role in biofilms emphasizes the diversity across different genera of the pro...
ORGANISM(S): Homo sapiens (Human) 
2023-03-22 | PXD039681 | Pride
Iob Mdpl Limosilactobacillus fermentum Muc5b Neuromedin Mog Lc-msms 
UnknownMitochondrial dysfunction in mandibular hypoplasia, deafness and progeroid features with concomitant lipodystrophy (MDPL) patients.
Not available
S-EPMC8908938 | biostudies-literature
UnknownTranscriptome profiling of human dermal MDPL fibroblasts reveals a characteristic molecular signature providing insights into pathogenic mechanisms.
Not available
S-EPMC12675696 | biostudies-literature
UnknownCharacterization of a highly conserved MUC5B-degrading protease, MdpL, from Limosilactobacillus fermentum.
Not available
S-EPMC10011156 | biostudies-literature
UnknownWhen do the pathological signs become evident? Study of human mesenchymal stem cells in MDPL syndrome.
Not available
S-EPMC11723661 | biostudies-literature
UnknownFunctional analysis of POLD1 p.ser605del variant: the aging phenotype of MDPL syndrome is associated with an impaired DNA repair capacity.
Not available
S-EPMC7950258 | biostudies-literature
UnknownStructural and functional impact of the POLD1 Ser605del variant in MDPL syndrome: insights from protein-protein interactions.
Not available
S-EPMC12606881 | biostudies-literature
UnknownMild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1.
Not available
S-EPMC9349287 | biostudies-literature
UnknownAnesthetic management of a patient with mandibular hypoplasia, deafness, progeroid features, lipodystrophy syndrome: a case report.
Not available
S-EPMC11466922 | biostudies-literature
UnknownA likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient.
Not available
S-EPMC9590123 | biostudies-literature
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