Primary Information |
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BoMiProt ID | Bomi8368 |
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Protein Name | Protein Mpv17 |
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Organism | Bos taurus |
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Uniprot ID | Q2KIN6 |
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Milk Fraction | Whey |
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Ref Sequence ID | NP_001039394.1 |
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Aminoacid Length | 176 |
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Molecular Weight | 19586 |
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FASTA Sequence |
Download |
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Gene Name | MPV17 |
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Gene ID | 505763 |
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Protein Existence Status | reviewed |
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Secondary Information |
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Protein Function | Human Mpv17-like protein (M-LPH/Mpv17L) is thought to play a role in minimizing mitochondrial dysfunction caused by mitochondrial DNA (mtDNA) damage |
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Biochemical Properties | A high degree of conservation has been determined between MPV17 and its mouse (Mpv17), zebrafish (tra) and yeast (SYM1) homologs, respectively, whereby mutants in these cause very different phenotypes. M-LPH, which has structural features atypical of PDE family members, might be a novel human PDE involved in cAMP/PKA signaling in the mitochondrial matrix. |
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Site(s) of PTM(s)
N-glycosylation,
O-glycosylation,
Phosphorylation
| NA |
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Predicted Disorder Regions | 1-7, 40-43, 80-87 |
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DisProt Annotation | |
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TM Helix Prediction | 3TMHs; (51-73),(94-116),(135-157) |
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Additional Comments | Mpv17 protein forms a channel in the inner mitochondrial membrane, allowing small molecules - in vertebrates probably nucleotides, and in yeast probably intermediates of the tricarboxylic acid cycle - to pass. |
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Bibliography | 1.Iida R, Ueki M, Yasuda T. Human Mpv17-like protein with a mitigating effect on mtDNA damage is involved in cAMP/PKA signaling in the mitochondrial matrix. Biochim Biophys Acta Mol Cell Res. 2020 Oct;1867(10):118792. doi: 10.1016/j.bbamcr.2020.118792. Epub 2020 Jul 2. PMID: 32621840. 2.Löllgen S, Weiher H. The role of the Mpv17 protein mutations of which cause mitochondrial DNA depletion syndrome (MDDS): lessons from homologs in different species. Biol Chem. 2015 Jan;396(1):13-25. doi: 10.1515/hsz-2014-0198. PMID: 25205723. |