Bioinformatic Screening of Autoimmune Disease Genes and Protein Structure Prediction with FAMS for Drug Discovery

被引:0
|
作者
Ishida, Shigeharu [1 ]
Umeyama, Hideaki [2 ]
Iwadate, Mitsuo [2 ]
Taguchi, Y-H. [1 ]
机构
[1] Chuo Univ, Dept Phys, Tokyo 1128551, Japan
[2] Chuo Univ, Dept Biol Sci, Tokyo 1128551, Japan
关键词
Autoimmune disease; drug discovery; FAMS; principal component analysis; promoter methylation; MONOZYGOTIC TWINS SUGGEST; HEPATOCYTE GROWTH-FACTOR; DNA METHYLATION; IMMUNE-RESPONSE; MOLECULAR PATHWAYS; MICROARRAY DATA; EXPRESSION; CANCER; PROFILES; DIFFERENTIATION;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autoimmune diseases are often intractable because their causes are unknown. Identifying which genes contribute to these diseases may allow us to understand the pathogenesis, but it is difficult to determine which genes contribute to disease. Recently, epigenetic information has been considered to activate/deactivate disease-related genes. Thus, it may also be useful to study epigenetic information that differs between healthy controls and patients with autoimmune disease. Among several types of epigenetic information, promoter methylation is believed to be one of the most important factors. Here, we propose that principal component analysis is useful to identify specific gene promoters that are differently methylated between the normal healthy controls and patients with autoimmune disease. Full Automatic Modeling System (FAMS) was used to predict the three-dimensional structures of selected proteins and successfully inferred relatively confident structures. Several possibilities of the application to the drug discovery based on obtained structures are discussed.
引用
收藏
页码:828 / 839
页数:12
相关论文
共 50 条
  • [1] Structure Prediction with FAMS for Proteins Screened Critically to Autoimmune Diseases based upon Bioinformatics
    Ishida, Shigeharu
    Umeyama, Hideaki
    Iwadate, Mitsuo
    Taguchi, Y-H.
    BIOINFORMATICS 2013: PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON BIOINFORMATICS MODELS, METHODS AND ALGORITHMS, 2013, : 261 - 267
  • [2] Advances in AI for Protein Structure Prediction: Implications for Cancer Drug Discovery and Development
    Qiu, Xinru
    Li, Han
    Ver Steeg, Greg
    Godzik, Adam
    BIOMOLECULES, 2024, 14 (03)
  • [3] Protein structure prediction in CASP6 using CHIMERA and FAMS
    Takeda-Shitaka, M
    Terashi, G
    Takaya, D
    Kanou, K
    Iwadate, M
    Umeyama, H
    PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2005, 61 : 122 - 127
  • [4] Understanding autoimmune disease: new targets for drug discovery
    Balogue, Cristina
    Kunkel, Steven L.
    Godessart, Nuria
    DRUG DISCOVERY TODAY, 2009, 14 (19-20) : 926 - 934
  • [5] Discovery of BVDU as a promising Drug for autoimmune diseases Therapy by Dendritic-cell-based functional screening
    Chen, Shuai
    Zhou, Jinfeng
    Cai, Yingying
    Zheng, Xinyuan
    Xie, Sirong
    Liao, Yuhan
    Zhu, Yu
    Qin, Chaoyan
    Lai, Weiming
    Yang, Cuixia
    Xie, Xin
    Du, Changsheng
    SCIENTIFIC REPORTS, 2017, 7
  • [6] Identification of Disease-Relevant Genes for Molecularly-Targeted Drug Discovery
    Kauselmann, G.
    Dopazo, A.
    Link, W.
    CURRENT CANCER DRUG TARGETS, 2012, 12 (01) : 1 - 13
  • [7] Integrating Computational Protein Function Prediction into Drug Discovery Initiatives
    Grant, Marianne A.
    DRUG DEVELOPMENT RESEARCH, 2011, 72 (01) : 4 - 16
  • [8] Protein-protein Docking and Hot-spot Prediction for Drug Discovery
    Grosdidier, Solene
    Fernandez-Recio, Juan
    CURRENT PHARMACEUTICAL DESIGN, 2012, 18 (30) : 4607 - 4618
  • [9] Cross-disease drug discovery based on bioinformatics and virtual screening: Study of key genes in Alzheimer's disease and ovarian cancer
    Shen, Ziyi
    Song, Jinxuan
    Wang, Shenglin
    Tang, Ming
    Yang, Yang
    Yu, Meiling
    Zhang, Rong
    Zhou, Honggui
    Jiang, Guohui
    GENE, 2025, 935
  • [10] Ligand docking and virtual screening in structure-based drug discovery
    Cavasotto, Claudio N.
    FROM PHYSICS TO BIOLOGY: THE INTERFACE BETWEEN EXPERIMENT AND COMPUTATION, 2006, 851 : 34 - 49