• 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

使用BAliBASE多序列比对测试集,通过SAM-T99评估蛋白质多序列比对。

Evaluation of protein multiple alignments by SAM-T99 using the BAliBASE multiple alignment test set.

作者信息

Karplus K, Hu B

机构信息

Computer Engineering, University of California, Santa Cruz, 59064, USA.

出版信息

Bioinformatics. 2001 Aug;17(8):713-20. doi: 10.1093/bioinformatics/17.8.713.

DOI:10.1093/bioinformatics/17.8.713
PMID:11524372
Abstract

MOTIVATION

SAM-T99 is an iterative hidden Markov model-based method for finding proteins similar to a single target sequence and aligning them. One of its main uses is to produce multiple alignments of homologs of the target sequence. Previous tests of SAM-T99 and its predecessors have concentrated on the quality of the searches performed, not on the quality of the multiple alignment. In this paper we report on tests of multiple alignment quality, comparing SAM-T99 to the standard multiple aligner, CLUSTALW.

RESULTS

The paper evaluates the multiple-alignment aspect of the SAM-T99 protocol, using the BAliBASE benchmark alignment database. On these benchmarks, SAM-T99 is comparable in accuracy with ClustalW.

AVAILABILITY

The SAM-T99 protocol can be run on the web at http://www.cse.ucsc.edu/research/compbio/HMM-apps/T99-query.html and the alignment tune-up option described here can be run at http://www.cse.ucsc.edu/research/compbio/HMM-apps/T99-tuneup.html. The protocol is also part of the standard SAM suite of tools. http://www.cse.ucsc.edu/research/compbio/sam/

摘要

动机

SAM-T99是一种基于迭代隐马尔可夫模型的方法,用于寻找与单个目标序列相似的蛋白质并进行比对。其主要用途之一是生成目标序列同源物的多序列比对。之前对SAM-T99及其前身的测试集中在搜索的质量上,而非多序列比对的质量。在本文中,我们报告了多序列比对质量的测试,将SAM-T99与标准多序列比对工具CLUSTALW进行比较。

结果

本文使用BAliBASE基准比对数据库评估了SAM-T99协议的多序列比对方面。在这些基准测试中,SAM-T99在准确性上与ClustalW相当。

可用性

SAM-T99协议可在网页http://www.cse.ucsc.edu/research/compbio/HMM-apps/T99-query.html上运行,此处描述的比对优化选项可在http://www.cse.ucsc.edu/research/compbio/HMM-apps/T99-tuneup.html上运行。该协议也是标准SAM工具套件的一部分。http://www.cse.ucsc.edu/research/compbio/sam/

相似文献

1
Evaluation of protein multiple alignments by SAM-T99 using the BAliBASE multiple alignment test set.使用BAliBASE多序列比对测试集,通过SAM-T99评估蛋白质多序列比对。
Bioinformatics. 2001 Aug;17(8):713-20. doi: 10.1093/bioinformatics/17.8.713.
2
Hidden Markov models for detecting remote protein homologies.用于检测远程蛋白质同源性的隐马尔可夫模型。
Bioinformatics. 1998;14(10):846-56. doi: 10.1093/bioinformatics/14.10.846.
3
Reduced space hidden Markov model training.简化空间隐马尔可夫模型训练
Bioinformatics. 1998 Jun;14(5):401-6. doi: 10.1093/bioinformatics/14.5.401.
4
Simultaneous sequence alignment and tree construction using hidden Markov models.使用隐马尔可夫模型进行同步序列比对和树构建。
Pac Symp Biocomput. 2003:180-91.
5
SAM-T08, HMM-based protein structure prediction.SAM-T08,基于隐马尔可夫模型的蛋白质结构预测。
Nucleic Acids Res. 2009 Jul;37(Web Server issue):W492-7. doi: 10.1093/nar/gkp403. Epub 2009 May 29.
6
OXBench: a benchmark for evaluation of protein multiple sequence alignment accuracy.OXBench:一种用于评估蛋白质多序列比对准确性的基准。
BMC Bioinformatics. 2003 Oct 10;4:47. doi: 10.1186/1471-2105-4-47.
7
A comparison of profile hidden Markov model procedures for remote homology detection.用于远程同源性检测的轮廓隐马尔可夫模型程序比较。
Nucleic Acids Res. 2002 Oct 1;30(19):4321-8. doi: 10.1093/nar/gkf544.
8
Calibrating E-values for hidden Markov models using reverse-sequence null models.使用反向序列空模型校准隐马尔可夫模型的E值。
Bioinformatics. 2005 Nov 15;21(22):4107-15. doi: 10.1093/bioinformatics/bti629. Epub 2005 Aug 25.
9
SATCHMO: sequence alignment and tree construction using hidden Markov models.SATCHMO:使用隐马尔可夫模型进行序列比对和树构建。
Bioinformatics. 2003 Jul 22;19(11):1404-11. doi: 10.1093/bioinformatics/btg158.
10
Weighting hidden Markov models for maximum discrimination.加权隐马尔可夫模型以实现最大区分度。
Bioinformatics. 1998;14(9):772-82. doi: 10.1093/bioinformatics/14.9.772.

引用本文的文献

1
Protein Structure Prediction: Challenges, Advances, and the Shift of Research Paradigms.蛋白质结构预测:挑战、进展与研究范式的转变
Genomics Proteomics Bioinformatics. 2023 Oct;21(5):913-925. doi: 10.1016/j.gpb.2022.11.014. Epub 2023 Mar 30.
2
HAlign-II: efficient ultra-large multiple sequence alignment and phylogenetic tree reconstruction with distributed and parallel computing.HAlign-II:利用分布式和并行计算实现高效的超大倍数序列比对及系统发育树重建
Algorithms Mol Biol. 2017 Sep 29;12:25. doi: 10.1186/s13015-017-0116-x. eCollection 2017.
3
Scalable Convex Multiple Sequence Alignment via Entropy-Regularized Dual Decomposition.
通过熵正则化对偶分解实现可扩展凸多序列比对
JMLR Workshop Conf Proc. 2017 Apr;54:1514-1522.
4
A Convex Atomic-Norm Approach to Multiple Sequence Alignment and Motif Discovery.一种用于多序列比对和基序发现的凸原子范数方法。
JMLR Workshop Conf Proc. 2016;48:2272-2280.
5
Enhancement of E. coli acyl-CoA synthetase FadD activity on medium chain fatty acids.大肠杆菌酰基辅酶A合成酶FadD对中链脂肪酸活性的增强作用。
PeerJ. 2015 Jun 30;3:e1040. doi: 10.7717/peerj.1040. eCollection 2015.
6
Evaluating the accuracy and efficiency of multiple sequence alignment methods.评估多序列比对方法的准确性和效率。
Evol Bioinform Online. 2014 Dec 7;10:205-17. doi: 10.4137/EBO.S19199. eCollection 2014.
7
SMURFLite: combining simplified Markov random fields with simulated evolution improves remote homology detection for beta-structural proteins into the twilight zone.SMURFLite:将简化的马尔可夫随机场与模拟进化相结合,可提高β结构蛋白远程同源检测的进入黄昏区的性能。
Bioinformatics. 2012 May 1;28(9):1216-22. doi: 10.1093/bioinformatics/bts110. Epub 2012 Mar 9.
8
BCL::contact-low confidence fold recognition hits boost protein contact prediction and de novo structure determination.BCL:低置信度折叠识别命中结果助力蛋白质接触预测和从头结构测定。
J Comput Biol. 2010 Feb;17(2):153-68. doi: 10.1089/cmb.2009.0030.
9
Benchmarking of TASSER_2.0: an improved protein structure prediction algorithm with more accurate predicted contact restraints.TASSER_2.0的基准测试:一种具有更准确预测接触限制的改进型蛋白质结构预测算法。
Biophys J. 2008 Aug;95(4):1956-64. doi: 10.1529/biophysj.108.129759. Epub 2008 May 16.
10
Discovering sequence motifs with arbitrary insertions and deletions.发现带有任意插入和缺失的序列基序。
PLoS Comput Biol. 2008 May 9;4(4):e1000071. doi: 10.1371/journal.pcbi.1000071.