Hidden Markov Models in Computational Biology

隐马尔可夫模型 假阳性悖论 计算机科学 蛋白质家族 珠蛋白 序列(生物学) 模式识别(心理学) 序列数据库 计算生物学 序列比对 集合(抽象数据类型) 人工智能 生物 遗传学 马尔可夫模型 蛋白质-蛋白质相互作用 系统生物学 肽序列 基因 程序设计语言
作者
Anders Krogh,Michael E. Brown,I. S Mian,Kimmen Sjölander,David Haussler
出处
期刊:Journal of Molecular Biology [Elsevier BV]
卷期号:235 (5): 1501-1531 被引量:1790
标识
DOI:10.1006/jmbi.1994.1104
摘要

Hidden Markov Models (HMMs) are applied to the problems of statistical modeling, database searching and multiple sequence alignment of protein families and protein domains. These methods are demonstrated on the globin family, the protein kinase catalytic domain, and the EF-hand calcium binding motif. In each case the parameters of an HMM are estimated from a training set of unaligned sequences. After the HMM is built, it is used to obtain a multiple alignment of all the training sequences. It is also used to search the SWISS-PROT 22 database for other sequences that are members of the given protein family, or contain the given domain. The HMM produces multiple alignments of good quality that agree closely with the alignments produced by programs that incorporate three-dimensional structural information. When employed in discrimination tests (by examining how closely the sequences in a database fit the globin, kinase and EF-hand HMMs), the HMM is able to distinguish members of these families from non-members with a high degree of accuracy. Both the HMM and PROFILESEARCH (a technique used to search for relationships between a protein sequence and multiply aligned sequences) perform better in these tests than PROSITE (a dictionary of sites and patterns in proteins). The HMM appears to have a slight advantage over PROFILESEARCH in terms of lower rates of false negatives and false positives, even though the HMM is trained using only unaligned sequences, whereas PROFILESEARCH requires aligned training sequences. Our results suggest the presence of an EF-hand calcium binding motif in a highly conserved and evolutionary preserved putative intracellular region of 155 residues in the alpha-1 subunit of L-type calcium channels which play an important role in excitation-contraction coupling. This region has been suggested to contain the functional domains that are typical or essential for all L-type calcium channels regardless of whether they couple to ryanodine receptors, conduct ions or both.

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