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SHARK:用于对内在无序和不可比对的蛋白质区域进行无比对同源性评估的网络服务器。

SHARK: web server for alignment-free homology assessment for intrinsically disordered and unalignable protein regions.

作者信息

Willis Chow Chi Fung, Scheremetjew Maxim, Moon HongKee, Ghosh Soumyadeep, Hadarovich Anna, Hersemann Lena, Toth-Petroczy Agnes

机构信息

Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.

Center for Systems Biology Dresden, Pfotenhauerstrasse 108, 01307 Dresden, Germany.

出版信息

Nucleic Acids Res. 2025 Jul 7;53(W1):W512-W519. doi: 10.1093/nar/gkaf408.

Abstract

Whereas alignment has been fundamental to sequence-based assessments of protein homology, it is ineffective for intrinsically disordered regions (IDRs) due to their lowered sequence conservation and unique sequence properties. Here, we present a web server implementation of SHARK (bio-shark.org), an alignment-free algorithm for homology classification that compares the overall amino acid composition and short regions (k-mers) shared between sequences (SHARK-scores). The output of such k-mer-based comparisons is used by SHARK-dive, a machine learning classifier to detect homology between unalignable, disordered sequences. SHARK-web provides sequence-versus-database assessment of protein sequence homology akin to conventional tools such as BLAST and HMMER. Additionally, we provide precomputed sets of IDR sequences from 16 model organism proteomes facilitating searches against species-specific IDR-omes. SHARK-dive offers superior overall homology detection performance to BLAST and HMMER, driven by a large increase in sensitivity to low sequence identity homologs, and can be used to facilitate the study of sequence-function relationships in disordered, difficult-to-align regions.

摘要

虽然序列比对一直是基于序列的蛋白质同源性评估的基础,但由于内在无序区域(IDR)的序列保守性较低和独特的序列特性,它对这些区域无效。在这里,我们展示了SHARK(bio-shark.org)的网络服务器实现,这是一种用于同源性分类的无比对算法,它比较序列之间共享的整体氨基酸组成和短区域(k-mer)(SHARK分数)。基于k-mer的这种比较的输出被SHARK-dive使用,SHARK-dive是一种机器学习分类器,用于检测不可比对的无序序列之间的同源性。SHARK-web提供类似于BLAST和HMMER等传统工具的蛋白质序列同源性的序列与数据库评估。此外,我们提供了来自16种模式生物蛋白质组的IDR序列预计算集,便于针对物种特异性IDR组进行搜索。SHARK-dive对低序列同一性同源物的敏感性大幅提高,从而提供了优于BLAST和HMMER的整体同源性检测性能,可用于促进对无序、难以比对区域中序列-功能关系的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/544a/12230711/6c1ef407a66d/gkaf408figgra1.jpg

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