CBLC Proteine (CBLC)

Human Cas-Br-M (Murine) Ecotropic Retroviral Transforming Sequence C (CBLC) Interaktionspartner

1. Methylmalonic aciduria with homocystinuria cblC is a multisystemic metabolic disease affecting cobalamin metabolism. The presence of retinal alterations in cblC is a common feature and it is reported to develop more frequently and into a more severe form in the early-onset phenotype, suggesting to some extent a correlation with the biochemical phenotype

2. Data suggest that ubiquitin ligase CBLC controls mostly network organization of the Golgi Apparatus.

3. Silencing of CBLC causes increased sensitivity to PARP1 inhibitor olaparib in breast cancer cell line models and that defective homologous recombination (HR) DNA repair is the likely cause.

4. the effects of two pathogenic missense mutations on the the catalytic activities of the human B12-processing chaperone CblC

5. This retrospective multicentre study evaluates clinical, biochemical and genetic findings in 88 cblC patients

6. The ubiquitin ligase activity of Cbl-c by the direct interaction of the LIM zinc coordinating domain of Hic5 is demonstrated.

7. the N terminus of Cbl-c contributes to the binding to the E2 and phosphorylation of Tyr-341 leads to a decrease in affinity and an increase in the E3 activity of Cbl-c

8. Data demonstrate that two E3 ligases of different classes, CBLC and AIP4, can interact and cooperate to down-regulate EGFR signaling.

9. c-Cbl is a negative regulator of hepatocyte growth factor/receptor tyrosine kinase Met signaling in B cells, mediating ubiquitination and, consequently, proteosomal degradation of Met, with a role in Met-mediated tumorigenesis.

10. Src is a preferential target of Cbl-c for degradation

11. ubiquitin protein ligase activity is regulated in c-Cbl by phosphorylation-induced conformational change and constitutive activation by tyrosine to glutamate point mutations

Cow (Bovine) Cas-Br-M (Murine) Ecotropic Retroviral Transforming Sequence C (CBLC) Interaktionspartner

1. bCblC, a bovine B12 trafficking chaperone, catalyzes elimination of the glutathione ligand from GSCbl by using the reduced form of glutathione (GSH).