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Computational analysis of human proteins addressing the relationship between intrinsic disorder and alternative splicing

Computational analysis of human proteins addressing the relationship between intrinsic disorder and alternative splicing
人类蛋白质的计算分析解决内在紊乱和选择性剪接之间的关系
批准号:
19310133
负责人:
NISHIKAWA Ken
金额:
$12.98万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2007
资助国家:
日本
项目状态:
已结题
起止时间:
2007 至 2009

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中文摘要
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英文摘要
For all human proteins encoded on the genome, we have succeeded to classify protein molecules into structured or intrinsically disordered (ID) regions using the method we developed in this project. As a result, we revealed the total fractions of ordered/disordered regions of human proteins at a first time. Analyzing locations of alternative splicing (AS) data along the protein sequence, we have also revealed that AS events occur in proportion to the fraction of ID regions of proteins.
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DOI: 10.1016/j.jmb.2007.02.033
发表时间: 2007-05-04
期刊: JOURNAL OF MOLECULAR BIOLOGY
影响因子: 5.6
作者: [Minezaki, Yoshiaki, Homma, Keiichi, Nishikawa, Ken]
通讯作者: Nishikawa, Ken
ヒトタンパク質の構造ドメイン・天然変性領域への区分
将人类蛋白质分类为结构域和自然变性区域
DOI: --
发表时间: 2008
期刊:
影响因子: --
作者: [福地佐斗志, 細田和男, 西川 建]
通讯作者: 西川 建
DOI: 10.1093/nar/gkn855
发表时间: 2009-01-01
期刊: NUCLEIC ACIDS RESEARCH
影响因子: 14.9
作者: [Fukuchi, Satoshi, Homma, Keiichi, Nishikawa, Ken]
通讯作者: Nishikawa, Ken
ミトコンドリア蛋白質は天然変性領域をもつか?
线粒体蛋白是否有自然变性区域?
DOI: --
发表时间: 2009
期刊:
影响因子: --
作者: [細田和男, 福地佐斗志, 西川建]
通讯作者: 西川建
10
    Developing a new protein homology-modeling method with high precision
    • 批准号:
      16201043
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $23.63万
    • 财政年份:
      2004
    • 负责人:
      NISHIKAWA Ken
    • 依托单位:
    Experimental study to verify structural changes of proteins taken place in the evolutionary process
    • 批准号:
      12480204
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $9.41万
    • 财政年份:
      2000
    • 负责人:
      NISHIKAWA Ken
    • 依托单位:
    海外基金