Calcium uptake protein 1

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (08:23, 22 April 2019) (edit) (undo)
 
(9 intermediate revisions not shown.)
Line 1: Line 1:
==Structure of MICU1==
==Structure of MICU1==
-
<StructureSection load='4NSC' size='340' side='right' caption='Caption for this structure' scene=''>
+
<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.
Line 32: Line 32:
== 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.
 +
 +
</StructureSection>
 +
 +
== 3D Structures of calcium uptake protein 1 ==
 +
 +
[[Calcium uptake protein 3D structures]]
== See Also ==
== See Also ==

Current revision

Contents

Structure of MICU1

Human mitochondrial calcium uptake protein 1 (PDB code 4nsc)

Drag the structure with the mouse to rotate

3D Structures of calcium uptake protein 1

Calcium uptake protein 3D structures

See Also

MCU : http://www.rcsb.org/pdb/gene/MCU
MICU 2 : http://www.rcsb.org/pdb/gene/MICU2

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

Proteopedia Page Contributors and Editors (what is this?)

Alexandra Helleux, Jaime Prilusky, Michal Harel

Personal tools