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大核苷酸序列中碱基配对的结构和组合限制

Structural and combinatorial constraints on base pairing in large nucleotide sequences.

作者信息

Nussinov R, Pieczenik G

出版信息

J Theor Biol. 1984 Feb 7;106(3):245-59. doi: 10.1016/0022-5193(84)90029-8.

Abstract

In this paper we discuss the constraints and combinatorial problems of folding long RNA and single stranded DNA molecules into base paired structures. A computer code FOLD-A was designed to perform base pairing foldings of very long sequence chains and search for low energy configurations. The logic of the FOLD-A algorithm is described in some detail. The applications of FOLD-A to the A-protein gene of MS2 and the whole genome of the phi X 174 phage with over 5300 bases are discussed in the accompanying paper.

摘要

在本文中,我们讨论了将长RNA和单链DNA分子折叠成碱基配对结构的限制因素和组合问题。设计了一个计算机程序FOLD-A来对非常长的序列链进行碱基配对折叠,并搜索低能量构型。详细描述了FOLD-A算法的逻辑。随附论文中讨论了FOLD-A在MS2的A蛋白基因以及含有超过5300个碱基的φX 174噬菌体全基因组中的应用。

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