The recent discovery of new genes, alternative splicing and protein-protein interactions between intracellular processing of vitamin B12 or cobalamin (Cbl) highlights the importance of an MS interactome. The goal of this PhD project is to further characterize the interactions of MS with other potential partners in a so-called MS interactome. Our data confirm for the first time in human cells (HepG2 cells and fibroblasts from cblC and cblG patients) various interactions that were so far only described in vitro or in bacteria: MS with methionine synthase reductase (MSR), MS with MMACHC, and MMACHC with MMADHC. Our data also reveal novel interactions: MMADHC with MTR, MMADHC with MSR, MSR with MMACHC and MS with MAT isoforms. Moreover, our dat...
Accès restreint aux membres de l'Université de Lorraine jusqu'au 2015-01-01A key factor of chemiores...
Vitamin B12 (cobalamin, Cbl) is required as a cofactor for two human enzymes: methylmalonyl-CoA muta...
Defects in the MMACHC gene represent the most common disorder of cobalamin (Cbl) metabolism, affecti...
The recent discovery of new genes, alternative splicing and protein-protein interactions between int...
La découverte récente de nouveaux gènes, de mécanismes d’épissage alternatif et d’interactions entre...
An increasing number of studies indicate that each step of the intracellular processing of vitamin B...
Vitamin B12 (cobalamin, Cbl) in its cofactor forms methyl-Cbl (MeCbl) and adenosyl-Cbl (AdoCbl), is ...
Conversion of vitamin B12 (cobalamin, Cbl) into the cofactor forms methyl-Cbl (MeCbl) and adenosyl-C...
International audienceThe cblG and cblC disorders of cobalamin (Cbl) metabolism are two inherited ca...
The cblG and cblC disorders of cobalamin (Cbl) metabolism are two inherited causes of megaloblastic ...
Vitamin B$_{12}$ (cobalamin, Cbl) is required as a cofactor by two human enzymes, 5-methyltetrahydro...
The cblD defect of intracellular vitamin B12 metabolism can lead to isolated methylmalonic aciduria ...
Vitamin B(12) (cobalamin, Cbl) is essential to the function of two human enzymes, methionine synthas...
Fibroblasts from patients with functional methionine synthase deficiency can be divided into 2 compl...
In humans vitamin B12 (cobalamin, Cbl) must be converted into two coenzyme forms, methylcobalamin (M...
Accès restreint aux membres de l'Université de Lorraine jusqu'au 2015-01-01A key factor of chemiores...
Vitamin B12 (cobalamin, Cbl) is required as a cofactor for two human enzymes: methylmalonyl-CoA muta...
Defects in the MMACHC gene represent the most common disorder of cobalamin (Cbl) metabolism, affecti...
The recent discovery of new genes, alternative splicing and protein-protein interactions between int...
La découverte récente de nouveaux gènes, de mécanismes d’épissage alternatif et d’interactions entre...
An increasing number of studies indicate that each step of the intracellular processing of vitamin B...
Vitamin B12 (cobalamin, Cbl) in its cofactor forms methyl-Cbl (MeCbl) and adenosyl-Cbl (AdoCbl), is ...
Conversion of vitamin B12 (cobalamin, Cbl) into the cofactor forms methyl-Cbl (MeCbl) and adenosyl-C...
International audienceThe cblG and cblC disorders of cobalamin (Cbl) metabolism are two inherited ca...
The cblG and cblC disorders of cobalamin (Cbl) metabolism are two inherited causes of megaloblastic ...
Vitamin B$_{12}$ (cobalamin, Cbl) is required as a cofactor by two human enzymes, 5-methyltetrahydro...
The cblD defect of intracellular vitamin B12 metabolism can lead to isolated methylmalonic aciduria ...
Vitamin B(12) (cobalamin, Cbl) is essential to the function of two human enzymes, methionine synthas...
Fibroblasts from patients with functional methionine synthase deficiency can be divided into 2 compl...
In humans vitamin B12 (cobalamin, Cbl) must be converted into two coenzyme forms, methylcobalamin (M...
Accès restreint aux membres de l'Université de Lorraine jusqu'au 2015-01-01A key factor of chemiores...
Vitamin B12 (cobalamin, Cbl) is required as a cofactor for two human enzymes: methylmalonyl-CoA muta...
Defects in the MMACHC gene represent the most common disorder of cobalamin (Cbl) metabolism, affecti...