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6XJV

MCU holocomplex in High-calcium state

Summary for 6XJV
Entry DOI10.2210/pdb6xjv/pdb
EMDB information22215
DescriptorCalcium uniporter protein, mitochondrial, Essential MCU regulator, mitochondrial, Calcium uptake protein 1, mitochondrial, ... (4 entities in total)
Functional Keywordsion channel, transport protein
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains20
Total formula weight619348.54
Authors
Wang, Y.,Jiang, Y. (deposition date: 2020-06-24, release date: 2020-09-09, Last modification date: 2024-03-06)
Primary citationWang, Y.,Han, Y.,She, J.,Nguyen, N.X.,Mootha, V.K.,Bai, X.C.,Jiang, Y.
Structural insights into the Ca 2+ -dependent gating of the human mitochondrial calcium uniporter.
Elife, 9:-, 2020
Cited by
PubMed Abstract: Mitochondrial Ca uptake is mediated by an inner mitochondrial membrane protein called the mitochondrial calcium uniporter. In humans, the uniporter functions as a holocomplex consisting of MCU, EMRE, MICU1 and MICU2, among which MCU and EMRE form a subcomplex and function as the conductive channel while MICU1 and MICU2 are EF-hand proteins that regulate the channel activity in a Ca-dependent manner. Here, we present the EM structures of the human mitochondrial calcium uniporter holocomplex (uniplex) in the presence and absence of Ca, revealing distinct Ca dependent assembly of the uniplex. Our structural observations suggest that Ca changes the dimerization interaction between MICU1 and MICU2, which in turn determines how the MICU1-MICU2 subcomplex interacts with the MCU-EMRE channel and, consequently, changes the distribution of the uniplex assemblies between the blocked and unblocked states.
PubMed: 32762847
DOI: 10.7554/eLife.60513
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.17 Å)
Structure validation

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