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      Backpropagation neural networks

      Chemometrics and Intelligent Laboratory Systems
      Elsevier BV

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          Increased rates of convergence through learning rate adaptation

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            Predicting the secondary structure of globular proteins using neural network models.

            We present a new method for predicting the secondary structure of globular proteins based on non-linear neural network models. Network models learn from existing protein structures how to predict the secondary structure of local sequences of amino acids. The average success rate of our method on a testing set of proteins non-homologous with the corresponding training set was 64.3% on three types of secondary structure (alpha-helix, beta-sheet, and coil), with correlation coefficients of C alpha = 0.41, C beta = 0.31 and Ccoil = 0.41. These quality indices are all higher than those of previous methods. The prediction accuracy for the first 25 residues of the N-terminal sequence was significantly better. We conclude from computational experiments on real and artificial structures that no method based solely on local information in the protein sequence is likely to produce significantly better results for non-homologous proteins. The performance of our method of homologous proteins is much better than for non-homologous proteins, but is not as good as simply assuming that homologous sequences have identical structures.
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              Improvements in protein secondary structure prediction by an enhanced neural network.

              Computational neural networks have recently been used to predict the mapping between protein sequence and secondary structure. They have proven adequate for determining the first-order dependence between these two sets, but have, until now, been unable to garner higher-order information that helps determine secondary structure. By adding neural network units that detect periodicities in the input sequence, we have modestly increased the secondary structure prediction accuracy. The use of tertiary structural class causes a marked increase in accuracy. The best case prediction was 79% for the class of all-alpha proteins. A scheme for employing neural networks to validate and refine structural hypotheses is proposed. The operational difficulties of applying a learning algorithm to a dataset where sequence heterogeneity is under-represented and where local and global effects are inadequately partitioned are discussed.
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                Author and article information

                Journal
                Chemometrics and Intelligent Laboratory Systems
                Chemometrics and Intelligent Laboratory Systems
                Elsevier BV
                01697439
                February 1993
                February 1993
                : 18
                : 2
                : 115-155
                Article
                10.1016/0169-7439(93)80052-J
                e43f6427-d58c-46f9-aa8b-2bf04397992b
                © 1993

                http://www.elsevier.com/tdm/userlicense/1.0/

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