• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在核苷酸序列数据库中寻找蛋白质相似性。

Finding protein similarities with nucleotide sequence databases.

作者信息

Henikoff S, Wallace J C, Brown J P

出版信息

Methods Enzymol. 1990;183:111-32. doi: 10.1016/0076-6879(90)83009-x.

DOI:10.1016/0076-6879(90)83009-x
PMID:2314271
Abstract

In this chapter we describe strategies for the searching of translated nucleotide sequence databases. By applying standard searching techniques developed for protein databases, we have found that previously unrecognized homologies can be detected. In addition, we have shown that extremely high sensitivity can be obtained using the scoring matrix strategy for short regions of similarity. The latter approach is particularly effective for detecting homologs found at the ends of sequences and within data of poor quality. These individual methods are demonstrated for the LysR family of bacterial activator proteins. Successive applications of these methods allow for sensitive detection of complex relationships, as demonstrated for the AraC family and for the complex LuxR-OmpR-NtrC families of bacterial activator proteins. Although our examples are drawn from bacterial sequences, these methods are likewise effective for higher eukaryotic genomic sequences, where protein-coding sequences are usually interrupted by introns. This should be particularly important in the future, since much of the expected increase in nucleotide sequence databases is likely to come from eukaryotic genomic sequencing projects.

摘要

在本章中,我们描述了搜索翻译后的核苷酸序列数据库的策略。通过应用为蛋白质数据库开发的标准搜索技术,我们发现可以检测到以前未识别的同源性。此外,我们已经表明,使用评分矩阵策略来处理短相似区域,可以获得极高的灵敏度。后一种方法对于检测序列末端和低质量数据中的同源物特别有效。这些方法分别在细菌激活蛋白的LysR家族中得到了验证。这些方法的连续应用能够灵敏地检测复杂关系,如在AraC家族以及细菌激活蛋白的复杂LuxR-OmpR-NtrC家族中所证明的那样。虽然我们的例子取自细菌序列,但这些方法同样适用于高等真核生物的基因组序列,在这些序列中蛋白质编码序列通常被内含子打断。这在未来应该会特别重要,因为核苷酸序列数据库预期的大量增长可能来自真核生物基因组测序项目。

相似文献

1
Finding protein similarities with nucleotide sequence databases.在核苷酸序列数据库中寻找蛋白质相似性。
Methods Enzymol. 1990;183:111-32. doi: 10.1016/0076-6879(90)83009-x.
2
A novel sequence similarity searching and visualization method based on overlappingly translated nucleic acids: the blastNP.一种基于重叠翻译核酸的新型序列相似性搜索与可视化方法:blastNP。
Med Hypotheses. 2004;62(4):568-74. doi: 10.1016/j.mehy.2003.11.020.
3
Searching for patterns in protein and nucleic acid sequences.寻找蛋白质和核酸序列中的模式。
Methods Enzymol. 1990;183:193-211. doi: 10.1016/0076-6879(90)83014-z.
4
Detection of protein similarities using nucleotide sequence databases.利用核苷酸序列数据库检测蛋白质相似性。
Nucleic Acids Res. 1988 Jul 11;16(13):6191-204. doi: 10.1093/nar/16.13.6191.
5
Rapid and sensitive sequence comparison with FASTP and FASTA.使用FASTP和FASTA进行快速灵敏的序列比对。
Methods Enzymol. 1990;183:63-98. doi: 10.1016/0076-6879(90)83007-v.
6
Large scale bacterial gene discovery by similarity search.通过相似性搜索进行大规模细菌基因发现。
Nat Genet. 1994 Jun;7(2):205-14. doi: 10.1038/ng0694-205.
7
BLAST and FASTA similarity searching for multiple sequence alignment.用于多序列比对的BLAST和FASTA相似性搜索。
Methods Mol Biol. 2014;1079:75-101. doi: 10.1007/978-1-62703-646-7_5.
8
Combined use of sequence similarity and codon bias for coding region identification.结合序列相似性和密码子偏好性进行编码区识别。
J Comput Biol. 1994 Spring;1(1):39-50. doi: 10.1089/cmb.1994.1.39.
9
Oligopeptide biases in protein sequences and their use in predicting protein coding regions in nucleotide sequences.蛋白质序列中的寡肽偏好及其在预测核苷酸序列中蛋白质编码区域的应用。
Proteins. 1988;4(2):99-122. doi: 10.1002/prot.340040204.
10
Use of homology domains in sequence similarity detection.在序列相似性检测中同源结构域的应用。
Methods Enzymol. 1990;183:133-46. doi: 10.1016/0076-6879(90)83010-7.

引用本文的文献

1
Fundamentals and Exceptions of the LysR-type Transcriptional Regulators.LysR 型转录调控因子的基础与例外。
ACS Synth Biol. 2024 Oct 18;13(10):3069-3092. doi: 10.1021/acssynbio.4c00219. Epub 2024 Sep 22.
2
MsmR1, a global transcription factor, regulates polymyxin synthesis and carbohydrate metabolism in SC2.MsmR1是一种全局转录因子,可调节SC2中的多粘菌素合成和碳水化合物代谢。
Front Microbiol. 2022 Nov 22;13:1039806. doi: 10.3389/fmicb.2022.1039806. eCollection 2022.
3
Engineering Bafilomycin High-Producers by Manipulating Regulatory and Biosynthetic Genes in the Marine Bacterium .
通过操纵海洋细菌中的调控和生物合成基因来工程化生产巴弗洛霉素的高产菌。
Mar Drugs. 2021 Jan 11;19(1):29. doi: 10.3390/md19010029.
4
structural analysis of quorum sensing genes in.群体感应基因的结构分析
Mol Biol Res Commun. 2015 Sep;4(3):115-124.
5
Interaction of the RcsB Response Regulator with Auxiliary Transcription Regulators in Escherichia coli.大肠杆菌中RcsB应答调节因子与辅助转录调节因子的相互作用
J Biol Chem. 2016 Jan 29;291(5):2357-70. doi: 10.1074/jbc.M115.696815. Epub 2015 Dec 3.
6
Transcriptional regulation by BglJ-RcsB, a pleiotropic heteromeric activator in Escherichia coli.BglJ-RcsB 通过转录调控,在大肠杆菌中作为一种多效性杂合激活剂。
Nucleic Acids Res. 2014 Mar;42(5):2999-3008. doi: 10.1093/nar/gkt1298. Epub 2013 Dec 13.
7
FK506 biosynthesis is regulated by two positive regulatory elements in Streptomyces tsukubaensis.FK506 生物合成受链霉菌中两个正调控元件的调控。
BMC Microbiol. 2012 Oct 19;12:238. doi: 10.1186/1471-2180-12-238.
8
Structural basis of photosensitivity in a bacterial light-oxygen-voltage/helix-turn-helix (LOV-HTH) DNA-binding protein.细菌光氧电压/螺旋-转角-螺旋(LOV-HTH)DNA 结合蛋白感光性的结构基础。
Proc Natl Acad Sci U S A. 2011 Jun 7;108(23):9449-54. doi: 10.1073/pnas.1100262108. Epub 2011 May 23.
9
Analysis and functional expression of NPP pathway-specific regulatory genes in Pseudonocardia autotrophica.分析和功能表达自养诺卡氏菌 NPP 途径特异性调节基因。
J Ind Microbiol Biotechnol. 2011 Apr;38(4):573-9. doi: 10.1007/s10295-011-0939-2. Epub 2011 Jan 23.
10
Functional roles for the GerE-family carboxyl-terminal domains of nitrate response regulators NarL and NarP of Escherichia coli K-12.大肠杆菌 K-12 硝酸盐应答调节蛋白 NarL 和 NarP 的 GerE 家族羧基末端结构域的功能作用。
Microbiology (Reading). 2010 Oct;156(Pt 10):2933-2943. doi: 10.1099/mic.0.040469-0. Epub 2010 Jul 15.