A novel method for quantitatively predicting non-covalent interactions from protein and nucleic acid sequence

被引:6
|
作者
Wu, Jiansheng [2 ]
Hu, Dong [2 ]
Xu, Xin [2 ]
Ding, Yan [1 ]
Yan, Shancheng [2 ]
Sun, Xiao [1 ]
机构
[1] Southeast Univ, State Key Lab Bioelect, Sch Biol Sci & Med Engn, Nanjing 210096, Peoples R China
[2] Nanjing Univ Posts & Telecommun, Sch Geog & Biol Informat, Nanjing 210046, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-covalent interactions; Support vector machine regression models; Conjoint triad; H-VDW; RANDOM FOREST MODEL; HYDROGEN-BONDS; COMPLEXES; FEATURES; PROGRAM;
D O I
10.1016/j.jmgm.2011.08.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biochemical interactions between proteins and biological macromolecules are dominated by noncovalent interactions. A novel method is presented for quantitatively predicting the number of two most dominant non-covalent interactions, i.e., hydrogen bonds and van der Waals contacts, potentially forming in a hypothetical protein-nucleic acid complex from sequences using support vector machine regression models in conjunction with a hybrid feature. The hybrid feature consists of the sequence-length fraction information, conjoint triad for protein sequences and the gapped dinucleotide composition. The SVR-based models achieved excellent performance. The polarity of amino acids was also found to play a vital role in the formation of hydrogen bonds and van der Waals contacts. We have constructed a web server H-VDW (http://www.cbi.seu.edu.cn/H-VDW/H-VDW.htm) for public access to the SVR models. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:28 / 34
页数:7
相关论文
共 50 条
  • [1] The detection of non-covalent interactions in nucleic acids using MALDI
    Lecchi, P
    Pannell, LK
    NEW METHODS FOR THE STUDY OF BIOMOLECULAR COMPLEXES, 1998, 510 : 217 - 224
  • [2] A non-covalent peptide-based strategy for protein and peptide nucleic acid transduction
    Gros, Edwige
    Deshayes, Sebastien
    Morris, May C.
    Aldrian-Herrada, Gudrun
    Depollier, Julien
    Heitz, Fredenic
    Divita, Gilles
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (03): : 384 - 393
  • [3] Sequence segregation improves non-covalent protein delivery
    Sgolastra, Federica
    Backlund, Coralie M.
    Ozay, E. Ilker
    Deronde, Brittany M.
    Minter, Lisa M.
    Tew, Gregory N.
    JOURNAL OF CONTROLLED RELEASE, 2017, 254 : 131 - 136
  • [4] Alignment of Non-Covalent Interactions at Protein-Protein Interfaces
    Zhu, Hongbo
    Sommer, Ingolf
    Lengauer, Thomas
    Domingues, Francisco S.
    PLOS ONE, 2008, 3 (04):
  • [5] Comparison of Non-Covalent and Covalent Interactions between Lactoferrin and Chlorogenic Acid
    Li, Zekun
    Al-Wraikat, Majida
    Hao, Changchun
    Liu, Yongfeng
    FOODS, 2024, 13 (08)
  • [6] Viscoelastic and thermoreversible networks crosslinked by non-covalent interactions between "clickable" nucleic acid oligomers and DNA
    Anderson, Alex J.
    Culver, Heidi R.
    Bryant, Stephanie J.
    Bowman, Christopher N.
    POLYMER CHEMISTRY, 2020, 11 (17) : 2959 - 2968
  • [7] COVALENT AND NON-COVALENT INTERACTIONS OF AFLATOXIN WITH DEFINED DEOXYRIBONUCLEIC-ACID SEQUENCES
    MISRA, RP
    MUENCH, KF
    HUMAYUN, MZ
    BIOCHEMISTRY, 1983, 22 (14) : 3351 - 3359
  • [8] Cationic nucleopeptides as novel non-covalent carriers for the delivery of peptide nucleic acid (PNA) and RNA oligomers
    Tomassi, Stefano
    Ierano, Caterina
    Mercurio, Maria Emilia
    Nigro, Ersilia
    Daniele, Aurora
    Russo, Rosita
    Chambery, Angela
    Baglivo, Ilaria
    Pedone, Paolo Vincenzo
    Rea, Giuseppina
    Napolitano, Maria
    Scala, Stefania
    Cosconati, Sandro
    Marinelli, Luciana
    Novellino, Ettore
    Messere, Anna
    Di Maro, Salvatore
    BIOORGANIC & MEDICINAL CHEMISTRY, 2018, 26 (09) : 2539 - 2550
  • [9] Computational study of lignin-protein non-covalent interactions
    Pandey, Jyotsna L.
    Watts, Heath D.
    Kubicki, James D.
    Richard, Tom L.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 245
  • [10] Characterization of Diverse Non-covalent Interactions Associated with Protein Acetylation
    Xu, Lingjia
    Zhang, Zhengyong
    Kong, Jilie
    CHEMICAL BIOLOGY & DRUG DESIGN, 2012, 80 (01) : 46 - 53