Calcium uptake protein 1
From Proteopedia
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==Structure of MICU1== | ==Structure of MICU1== | ||
- | <StructureSection load='4NSC' size='340' side=' | + | <StructureSection load='4NSC' size='340' side='left' caption='Human mitochondrial calcium uptake protein 1 (PDB code [[4nsc]])' scene=''> |
- | MICU 1 (Mitochondrial Calcium Uptake 1) is a key regulator of mitochondrial calcium uniporter (MCU) required to increase calcium uptake by MCU when cytoplasmic calcium is high. | + | '''MICU 1''' ('''Mitochondrial Calcium Uptake Protein 1''') is a key regulator of mitochondrial calcium uniporter (MCU) required to increase calcium uptake by MCU when cytoplasmic calcium is high. |
It also regulates glucose-dependent insulin secretion in pancreatic beta-cells by regulating mitochondrial calcium uptake. | It also regulates glucose-dependent insulin secretion in pancreatic beta-cells by regulating mitochondrial calcium uptake. | ||
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== Disease == | == Disease == | ||
If MICU1 gene is modified, Ca2+ can be load in higher concentration in the mitochondry resulting Myopathy with extrapyramidal signs (MPXPS). This is an autosomal recessive disorder characterized by early-onset proximal muscle weakness with a static course and moderately to grossly elevated serum creatine kinase levels accompanied by learning difficulties. Most patients develop subtle extrapyramidal motor signs that progress to a debilitating disorder of involuntary movement with variable features, including chorea, tremor, dystonic posturing and orofacial dyskinesia. Additional variable features include ataxia, microcephaly, ophthalmoplegia, ptosis, optic atrophy and axonal peripheral neuropathy. | If MICU1 gene is modified, Ca2+ can be load in higher concentration in the mitochondry resulting Myopathy with extrapyramidal signs (MPXPS). This is an autosomal recessive disorder characterized by early-onset proximal muscle weakness with a static course and moderately to grossly elevated serum creatine kinase levels accompanied by learning difficulties. Most patients develop subtle extrapyramidal motor signs that progress to a debilitating disorder of involuntary movement with variable features, including chorea, tremor, dystonic posturing and orofacial dyskinesia. Additional variable features include ataxia, microcephaly, ophthalmoplegia, ptosis, optic atrophy and axonal peripheral neuropathy. | ||
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+ | </StructureSection> | ||
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+ | == 3D Structures of calcium uptake protein 1 == | ||
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+ | [[Calcium uptake protein 3D structures]] | ||
== See Also == | == See Also == |
Current revision
Contents |
Structure of MICU1
|
3D Structures of calcium uptake protein 1
Calcium uptake protein 3D structures
See Also
References
- https://www.researchgate.net/publication/260152737_Structural_and_mechanistic_insights_into_MICU1_regulation_of_mitochondrial_calcium_uptake
- http://ghr.nlm.nih.gov/gene/MICU1
- http://www.rcsb.org/pdb/home/home.do
- http://www.uniprot.org/uniprot/Q9BPX6