5HSP
MamM CTD M250L
5HSP の概要
エントリーDOI | 10.2210/pdb5hsp/pdb |
分子名称 | Magnetosome protein MamM, SULFATE ION (3 entities in total) |
機能のキーワード | cation diffusion facilitator, metal transport |
由来する生物種 | Magnetospirillum gryphiswaldense |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 27755.02 |
構造登録者 | |
主引用文献 | Barber-Zucker, S.,Uebe, R.,Davidov, G.,Navon, Y.,Sherf, D.,Chill, J.H.,Kass, I.,Bitton, R.,Schuler, D.,Zarivach, R. Disease-Homologous Mutation in the Cation Diffusion Facilitator Protein MamM Causes Single-Domain Structural Loss and Signifies Its Importance. Sci Rep, 6:31933-31933, 2016 Cited by PubMed Abstract: Cation diffusion facilitators (CDF) are highly conserved, metal ion efflux transporters that maintain divalent transition metal cation homeostasis. Most CDF proteins contain two domains, the cation transporting transmembrane domain and the regulatory cytoplasmic C-terminal domain (CTD). MamM is a magnetosome-associated CDF protein essential for the biomineralization of magnetic iron-oxide particles in magnetotactic bacteria. To investigate the structure-function relationship of CDF cytoplasmic domains, we characterized a MamM M250P mutation that is synonymous with the disease-related mutation L349P of the human CDF protein ZnT-10. Our results show that the M250P exchange in MamM causes severe structural changes in its CTD resulting in abnormal reduced function. Our in vivo, in vitro and in silico studies indicate that the CTD fold is critical for CDF proteins' proper function and support the previously suggested role of the CDF cytoplasmic domain as a CDF regulatory element. Based on our results, we also suggest a mechanism for the effects of the ZnT-10 L349P mutation in human. PubMed: 27550551DOI: 10.1038/srep31933 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.79 Å) |
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