Literature DB >> 10584219

Application of multivariate data analysis methods to comparative molecular field analysis (CoMFA) data: proton affinities and pKa prediction for nucleic acids components.

R Gargallo1, C A Sotriffer, K R Liedl, B M Rode.   

Abstract

Multivariate data analysis methods (Principal Component Analysis (PCA) and Partial Least Squares (PLS)) are applied to the analysis of the CoMFA (Comparative Molecular Field Analysis) data for several nucleic acids components. The data set includes nitrogenated bases, nucleosides, linear nucleotides, 3', 5'-cyclic nucleotides and oligonucleotides. PCA is applied to study the structure of the CoMFA data and to detect possible outliers in the data set. PLS is applied to correlate the CoMFA data with either calculated AM1 proton affinities or with experimental pKa values. The possibility of making a prediction of pKa values directly from 3D structures of the monomers for polynucleotides is also shown. The influence of the superposition criteria and of conformational changes along the glycosidic bond on the pKa prediction are studied as well.

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Year:  1999        PMID: 10584219     DOI: 10.1023/a:1008005522776

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  4 in total

1.  Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins.

Authors:  R D Cramer; D E Patterson; J D Bunce
Journal:  J Am Chem Soc       Date:  1988-08-01       Impact factor: 15.419

2.  Sites and thermodynamic quantities associated with proton and metal ion interaction with ribonucleic acid, deoxyribonucleic acid, and their constituent bases, nucleosides, and nucleotides.

Authors:  R M Izatt; J J Christensen; J H Rytting
Journal:  Chem Rev       Date:  1971-10       Impact factor: 60.622

3.  3D-quantitative structure-activity relationships of human immunodeficiency virus type-1 proteinase inhibitors: comparative molecular field analysis of 2-heterosubstituted statine derivatives-implications for the design of novel inhibitors.

Authors:  R T Kroemer; P Ettmayer; P Hecht
Journal:  J Med Chem       Date:  1995-12-08       Impact factor: 7.446

4.  Direct prediction of dissociation constants (pKa's) of clonidine-like imidazolines, 2-substituted imidazoles, and 1-methyl-2-substituted-imidazoles from 3D structures using a comparative molecular field analysis (CoMFA) approach.

Authors:  K H Kim; Y C Martin
Journal:  J Med Chem       Date:  1991-07       Impact factor: 7.446

  4 in total
  1 in total

1.  Prediction of pK(a) for neutral and basic drugs based on radial basis function Neural networks and the heuristic method.

Authors:  Feng Luan; Weiping Ma; Haixia Zhang; Xiaoyun Zhang; Mancang Liu; Zhide Hu; Botao Fan
Journal:  Pharm Res       Date:  2005-08-24       Impact factor: 4.200

  1 in total

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