,OCTN2

Johannes Jokiel1, Marcel Bermudez1

  • 1Institute of Pharmaceutical and Medicinal Chemistry, University of Münster, Corrensstr. 48, 48149, Muenster, Germany.

Molecular informatics
|January 15, 2025
PubMed
概括

原发性肉氨酸缺乏症 (PCD) 是一种影响肉氨酸运输的遗传性疾病. 这项研究使用结构建模来揭示OCTN2载体的突变如何影响蛋白质动态和肉氨酸运输.

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