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5HSP

MamM CTD M250L

5HSP の概要
エントリーDOI10.2210/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
Barber-Zucker, S.,Zarivach, R. (登録日: 2016-01-26, 公開日: 2016-11-30, 最終更新日: 2024-01-10)
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: 27550551
DOI: 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)
構造検証レポート
Validation report summary of 5hsp
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-13に公開中

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