4XSJ
Crystal structure of the N-terminal domain of the human mitochondrial calcium uniporter fused with T4 lysozyme
Summary for 4XSJ
Entry DOI | 10.2210/pdb4xsj/pdb |
Descriptor | Lysozyme,Calcium uniporter protein, mitochondrial, SULFATE ION (3 entities in total) |
Functional Keywords | membrane protein, calcium channel, mitochondria, transport protein |
Biological source | Enterobacteria phage T4 More |
Cellular location | Mitochondrion inner membrane ; Multi-pass membrane protein : Q8NE86 |
Total number of polymer chains | 1 |
Total formula weight | 30076.32 |
Authors | Lee, Y.,Min, C.K.,Kim, T.G.,Song, H.K.,Lim, Y.,Kim, D.,Shin, K.,Kang, M.,Kang, J.Y.,Youn, H.-S.,Lee, J.-G.,An, J.Y.,Park, K.R.,Lim, J.J.,Kim, J.H.,Kim, J.H.,Park, Z.Y.,Kim, Y.-S.,Wang, J.,Kim, D.H.,Eom, S.H. (deposition date: 2015-01-22, release date: 2015-09-16, Last modification date: 2023-11-08) |
Primary citation | Lee, Y.,Min, C.K.,Kim, T.G.,Song, H.K.,Lim, Y.,Kim, D.,Shin, K.,Kang, M.,Kang, J.Y.,Youn, H.S.,Lee, J.G.,An, J.Y.,Park, K.R.,Lim, J.J.,Kim, J.H.,Kim, J.H.,Park, Z.Y.,Kim, Y.S.,Wang, J.,Kim, D.H.,Eom, S.H. Structure and function of the N-terminal domain of the human mitochondrial calcium uniporter. Embo Rep., 16:1318-1333, 2015 Cited by PubMed Abstract: The mitochondrial calcium uniporter (MCU) is responsible for mitochondrial calcium uptake and homeostasis. It is also a target for the regulation of cellular anti-/pro-apoptosis and necrosis by several oncogenes and tumour suppressors. Herein, we report the crystal structure of the MCU N-terminal domain (NTD) at a resolution of 1.50 Å in a novel fold and the S92A MCU mutant at 2.75 Å resolution; the residue S92 is a predicted CaMKII phosphorylation site. The assembly of the mitochondrial calcium uniporter complex (uniplex) and the interaction with the MCU regulators such as the mitochondrial calcium uptake-1 and mitochondrial calcium uptake-2 proteins (MICU1 and MICU2) are not affected by the deletion of MCU NTD. However, the expression of the S92A mutant or a NTD deletion mutant failed to restore mitochondrial Ca(2+) uptake in a stable MCU knockdown HeLa cell line and exerted dominant-negative effects in the wild-type MCU-expressing cell line. These results suggest that the NTD of MCU is essential for the modulation of MCU function, although it does not affect the uniplex formation. PubMed: 26341627DOI: 10.15252/embr.201540436 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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