THE USE OF SIDE-CHAIN PACKING METHODS IN MODELING BACTERIOPHAGE REPRESSOR AND CRO PROTEINS

被引:20
|
作者
CHUNG, SY [1 ]
SUBBIAH, S [1 ]
机构
[1] STANFORD UNIV,SCH MED,DEPT BIOL STRUCT,STANFORD,CA 94305
关键词
HOMOLOGY MODELING; REPRESSOR AND CRO PROTEINS; RMS DEVIATIONS; SIDE-CHAIN PACKING METHODS; TORSION ANGLES;
D O I
10.1002/pro.5560041107
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
In recent years, it has been repeatedly demonstrated that the coordinates of the main-chain atoms alone are sufficient to determine the side-chain conformations of buried residues of compact proteins. Given a perfect backbone, the side-chain packing method can predict the side-chain conformations to an accuracy as high as 1.2 Angstrom RMS deviation (RMSD) with greater than 80% of the (chi) angles correct. However, similarly rigorous studies have not been conducted to determine how well these apply, if at all, to the more important problem of homology modeling per se. Specifically, if the available backbone is imperfect, as expected for practical application of homology modeling, can packing constraints alone achieve sufficiently accurate predictions to be useful? Here, by systematically applying such methods to the pairwise modeling of two repressor and two cro proteins from the closely related bacteriophages 434 and P22, we find that when the backbone RMSD is 0.8 Angstrom, the prediction on buried side chain is accurate with an RMS error of 1.8 Angstrom and approximately 70% of the (chi) angles correctly predicted. When the backbone RMSD is larger, in the range of 1.6-1.8 Angstrom, the prediction quality is still significantly better than random, with RMS error at 2.2 Angstrom on the buried side chains and 60% accuracy on (chi) angles. Together these results suggest the following rules-of-thumb for homology modeling of buried side chains. When the sequence identity between the modeled sequence and the template sequence is > 50% (or, equivalently, the expected backbone RMSD is < 1 Angstrom), side-chain packing methods work well. When sequence identity is between 30-50%, reflecting a backbone RMS error of 1-2 Angstrom, it is still valid to use side-chain packing methods to predict the buried residues, albeit with care. When sequence identity is below 30% (or backbone RMS error greater than 2 Angstrom), the backbone constraint alone is unlikely to produce useful models. Other methods, such as those involving the use of database fragments to reconstruct a template backbone, may be necessary as a complementary guide for modeling.
引用
收藏
页码:2300 / 2309
页数:10
相关论文
共 7 条
  • [1] MODELING SIDE-CHAIN CONFORMATION FOR HOMOLOGOUS PROTEINS USING AN ENERGY-BASED ROTAMER SEARCH
    WILSON, C
    GREGORET, LM
    AGARD, DA
    JOURNAL OF MOLECULAR BIOLOGY, 1993, 229 (04) : 996 - 1006
  • [2] Closing the side-chain gap in protein loop modeling
    Karen A. Rossi
    Akbar Nayeem
    Carolyn A. Weigelt
    Stanley R. Krystek
    Journal of Computer-Aided Molecular Design, 2009, 23 : 411 - 418
  • [3] Closing the side-chain gap in protein loop modeling
    Rossi, Karen A.
    Nayeem, Akbar
    Weigelt, Carolyn A.
    Krystek, Stanley R.
    JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 2009, 23 (07) : 411 - 418
  • [4] Cytochrome P450 side-chain cleavage: Insights gained from homology modeling
    Storbeck, Karl-Heinz
    Swart, Pieter
    Swart, Amanda C.
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2007, 265 : 65 - 70
  • [5] SPINFAST: Using structure alignment profiles to enhance the accuracy and assess the reliability of protein side-chain modeling
    Poleksic, Aleksandar
    Danzer, Joseph F.
    Palmer, Brian A.
    Olafson, Barry D.
    Debe, Derek A.
    PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2006, 65 (04) : 953 - 958
  • [6] Prediction of protein side-chain rotamers from a backbone-dependent rotamer library: A new homology modeling tool
    Bower, MJ
    Cohen, FE
    Dunbrack, RL
    JOURNAL OF MOLECULAR BIOLOGY, 1997, 267 (05) : 1268 - 1282
  • [7] Determining Valine Side-Chain Rotamer Conformations in Proteins from Methyl 13C Chemical Shifts: Application to the 360 kDa Half-Proteasome
    Hansen, D. Flemming
    Kay, Lewis E.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (21) : 8272 - 8281