SignatureFinder使序列挖掘识别钴胺依赖的光感受器蛋白。

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
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引用次数: 0

摘要

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。
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SignatureFinder enables sequence mining to identify cobalamin-dependent photoreceptor proteins.

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.

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