SignatureFinder enables sequence mining to identify cobalamin-dependent photoreceptor proteins

IF 4.2 The FEBS journal Pub Date : 2024-12-24 DOI:10.1111/febs.17377
Yuqi Yu, Laura N. Jeffreys, Harshwardhan Poddar, Adam Hill, Linus Johannissen, Fanzhuo Dai, Michiyo Sakuma, David Leys, Derren J. Heyes, Shaowei Zhang, Nigel S. Scrutton
{"title":"SignatureFinder enables sequence mining to identify cobalamin-dependent photoreceptor proteins","authors":"Yuqi Yu,&nbsp;Laura N. Jeffreys,&nbsp;Harshwardhan Poddar,&nbsp;Adam Hill,&nbsp;Linus Johannissen,&nbsp;Fanzhuo Dai,&nbsp;Michiyo Sakuma,&nbsp;David Leys,&nbsp;Derren J. Heyes,&nbsp;Shaowei Zhang,&nbsp;Nigel S. Scrutton","doi":"10.1111/febs.17377","DOIUrl":null,"url":null,"abstract":"<p>Photoreceptors control cellular processes in response to light. Most photoreceptors sense blue or red light, but the recent discovery of the cobalamin-dependent photoreceptor, CarH, has expanded the wavelength range of photoreception to other regions of the electromagnetic spectrum to include the green light region. Further identification of cobalamin-dependent green light-sensitive photoreceptors has been hampered owing to poor annotation of the light responsiveness of cobalamin-binding domains (CBDs) in public databases. Here we report a computational workflow, <i>SignatureFinder</i>, that uses a combination of sequence and structural analyses to identify new light-responsive CBD-containing proteins. The light response of exemplar proteins containing the proposed signature were confirmed experimentally. A structural analysis of these new photoreceptors, including the crystal structure of a new CBD domain, highlights how the signature elements interact with the cobalamin chromophore to sense light. Database mining of 128 000 CBD-containing sequences using the identified signature revealed more diverse CBD-containing photoreceptors, thereby expanding the family of green-light photoreceptors. A <i>SignatureFinder</i> web server is available (https://enzymeevolver.com) for wider applications, including the identification of signature sequences of other biological ligands of interest.</p>","PeriodicalId":94226,"journal":{"name":"The FEBS journal","volume":"292 3","pages":"635-652"},"PeriodicalIF":4.2000,"publicationDate":"2024-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/febs.17377","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The FEBS journal","FirstCategoryId":"1085","ListUrlMain":"https://febs.onlinelibrary.wiley.com/doi/10.1111/febs.17377","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Photoreceptors control cellular processes in response to light. Most photoreceptors sense blue or red light, but the recent discovery of the cobalamin-dependent photoreceptor, CarH, has expanded the wavelength range of photoreception to other regions of the electromagnetic spectrum to include the green light region. Further identification of cobalamin-dependent green light-sensitive photoreceptors has been hampered owing to poor annotation of the light responsiveness of cobalamin-binding domains (CBDs) in public databases. Here we report a computational workflow, SignatureFinder, that uses a combination of sequence and structural analyses to identify new light-responsive CBD-containing proteins. The light response of exemplar proteins containing the proposed signature were confirmed experimentally. A structural analysis of these new photoreceptors, including the crystal structure of a new CBD domain, highlights how the signature elements interact with the cobalamin chromophore to sense light. Database mining of 128 000 CBD-containing sequences using the identified signature revealed more diverse CBD-containing photoreceptors, thereby expanding the family of green-light photoreceptors. A SignatureFinder web server is available (https://enzymeevolver.com) for wider applications, including the identification of signature sequences of other biological ligands of interest.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
SignatureFinder使序列挖掘识别钴胺依赖的光感受器蛋白。
光感受器控制细胞对光的反应过程。大多数光感受器感知蓝光或红光,但最近发现的依赖钴胺素的光感受器CarH将光感受器的波长范围扩展到电磁波谱的其他区域,包括绿光区域。由于公共数据库中对钴胺结合域(CBDs)光响应性的注释不足,进一步鉴定钴胺依赖的绿光敏感光感受器受到阻碍。在这里,我们报告了一个计算工作流程,SignatureFinder,它使用序列和结构分析的组合来识别新的光响应的含有cbd的蛋白质。实验证实了包含该特征的范例蛋白的光响应。对这些新的光感受器的结构分析,包括新的CBD结构域的晶体结构,突出了特征元素如何与钴胺素发色团相互作用以感知光。利用所识别的特征对128000个含cbd序列进行数据库挖掘,揭示了更多的含cbd光感受器,从而扩大了绿光光感受器家族。SignatureFinder web服务器(https://enzymeevolver.com)可用于更广泛的应用,包括识别其他感兴趣的生物配体的签名序列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
SLC38A6 expression in renal tubular cells accelerates cisplatin-induced acute kidney injury by promoting cell apoptosis. Contrasting effects of different molecular crowding environments on base-pair opening/closing dynamics of DNA triplex structures. Tyrosine residues at the substrate binding site in human NQO1 homodimer: Protein conformational dynamics and optimization of substrate binding geometry. Genetic dissection reveals distinct contributions of the eS31 N-terminal domain to translational accuracy in Saccharomyces cerevisiae. Sterol binding mechanism of a plant START-like domain: A new sterol transport paradigm via an amphiphilic cavity.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1