| アイテムタイプ |
学術雑誌論文 / Journal Article(1) |
| 公開日 |
2024-03-26 |
| タイトル |
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タイトル |
1H, 13C and 15N backbone and side?chain resonance assignments of the human oncogenic protein NCYM |
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言語 |
en |
| 言語 |
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言語 |
eng |
| 資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
| 著者 |
Mouhand Assla
Nakatani Kazuma
Kono Fumiaki
Hippo Yoshitaka
Matsuo Tatsuhito
Barthe Philippe
Peters Judith
Suenaga Yusuke
Tamada Taro
Roumestand Christian
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| 抄録 |
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内容記述タイプ |
Abstract |
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内容記述 |
NCYM is a cis-antisense gene of MYCN oncogene and encodes an oncogenic protein that stabilizes MYCN via inhibition of GSK3b. High NCYM expression levels are associated with poor clinical outcomes in human neuroblastomas, and NCYM overexpression promotes distant metastasis in animal models of neuroblastoma. Using vacuum-ultraviolet circular dichroism and small-angle X-ray scattering, we previously showed that NCYM has high flexibility with partially folded structures; however, further structural characterization is required for the design of anti-cancer agents targeting NCYM. Here we report the 1H, 15N and 13C nuclear magnetic resonance assignments of NCYM. Secondary structure prediction using Secondary Chemical Shifts and TALOS-N analysis demonstrates that the structure of NCYM is essentially disordered, even though residues in the central region of the peptide clearly present a propensity to adopt a dynamic helical structure. This preliminary study provides foundations for further analysis of interaction between NCYM and potential partners. |
| 書誌情報 |
Biomolecular NMR Assignments
発行日 2024-03
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| DOI |
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識別子タイプ |
DOI |
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関連識別子 |
10.1007/s12104-024-10169-3 |
