anti-PIMT (PCMT1) Antikörper

Human PIMT (PCMT1) Interaktionspartner

1. decrease of PCMT1 significantly increased the proportion of D-Asp (zeige ASIP Antikörper) residues in PHB1 (zeige PHB Antikörper) and had significant and fatal impacts on morphology and functions of the mitochondria, such as ATP production and the mitochondrial fusion-fission system

2. PIMT heterozygosity for R36C, G175R, R17H, or R17S would be detrimental to successful aging, whereas homozygosity (should it ever occur) would produce devastating neuropathology

3. Strong PIMT expression was a predictive marker of poor prognosis for surgically resected lung adenocarcinoma.

4. The data of this study indicated that DA-associated PIMT downregulation is an important event contributing to neuronal cell death

5. ERK2 (zeige MAPK1 Antikörper)-mediated phosphorylation of transcriptional coactivator binding protein PIMT/NCoA6IP (zeige TGS1 Antikörper) at Ser298 augments hepatic gluconeogenesis.

6. Overexpression of PCMT1 attentuates Mst1 (zeige MST1 Antikörper) kinase activation and its apoptotic effects in response to hypoxia-induced injury in cardiomyocytes.

7. Data indicate that human PROTEIN ISOASPARTYL METHYLTRANSFERASE (PIMT) can initiate isoAsp conversion to Asp (zeige ASIP Antikörper), and is able to restore Arabidopsis PRH75 (zeige DDX46 Antikörper)'s complex biochemical activity provided isoAsp formation has not led to conformational alterations.

8. Data show six differentially expressed proteins were identified as HSP70 (zeige HSP70 Antikörper), PPIA (zeige PPIA Antikörper) and alpha-Enolase (up-regulated) S100-A9, PIMT and beta-5 tubulin (zeige TUBB Antikörper) (down-regulated), most of which had been shown to play a potential role in the pathogenesis of atherosclerosis.

9. The results implied that maternal polymorphisms in PCMT1 might be a potential genetic risk factor for isolated anencephaly in the Chinese population of Lvliang.

10. Study provides new insight into the molecular mechanisms by which PIMT suppresses the p53 (zeige TP53 Antikörper) activity through carboxyl methylation, and suggests a therapeutic target for cancers.

Mouse (Murine) PIMT (PCMT1) Interaktionspartner

1. Loss of normal CKB (zeige CHKB Antikörper) structure and function contributes to the mechanisms by which isoaspartate accumulation leads to central nervous system dysfunction in the PIMT-Knockout mouse.

2. PIMT levels may significantly influence the course of age-related central nervous system dysfunction.

3. ERK2 (zeige MAPK1 Antikörper)-mediated phosphorylation of transcriptional coactivator binding protein PIMT/NCoA6IP (zeige TGS1 Antikörper) at Ser298 augments hepatic gluconeogenesis.

4. PIMT knockout mice have perturbations in glutamate (zeige GRIN1 Antikörper) metabolism in the brain and die prematurely of epileptic seizures.

5. synuclein is not a major target of PIMT in vivo

6. Altered levels of S-adenosylmethionine and S-adenosylhomocysteine in the brains of PCMT1 knockout mice

7. Recombinant adeno (zeige ADORA2A Antikörper)-PIMT improved the symptoms of PIMT-deficient mice in vivo, but only partially repaired IsoAsp in damaged proteins.

8. An accumulation of isoaspartyl residues in cells of mice lacking the isoaspartyl repair enzyme PCMT alters the effector function of T lymphocytes leading to autoantibody production.

9. Pcmt1-/- mice have altered regulation of the insulin (zeige INS Antikörper) pathway, possibly as a compensatory response to altered glucose uptake or metabolism or as an adaptive response to a general accumulation of isoaspartyl protein damage in the brain and other tissues.

10. Protein L-isoaspartyl methyltransferase (PIMT) catalyzes in vivo racemization of Asp (zeige C3 Antikörper)-25 in mammalian histone H2B, suggesting that PIMT functions in the repair, rather than the metabolic turnover, of isoaspartyl proteins in vivo.