<scp> <i>SignatureFinder</i> </scp> 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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Publication Details

Journal
FEBS Journal
Published
2024-12-24
DOI
https://doi.org/10.1111/febs.17377
Citations
3
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
0.70

Funders

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article

SignatureFinder enables sequence mining to identify cobalamin‐dependent photoreceptor proteins

Adam Hill, David Leys, Derren J. Heyes, Linus O. Johannissen et al.
3 citations
FEBS Journal
Photosynthetic Processes and Mechanisms
0.70
article

SignatureFinder enables sequence mining to identify cobalamin‐dependent photoreceptor proteins

Adam Hill, David Leys, Derren J. Heyes, Linus O. Johannissen, Michiyo Sakuma, Harshwardhan Poddar, Laura N. Jeffreys, Yuqi Yu, Nigel Shaun Scrutton, Fengyuan Dai, Shaowei Zhang
article en
3 citations

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.

FEBS JournalVol. 292(3)
University of Manchester (GB)
Engineering and Physical Sciences Research Council
No poverty
Openalex Percentile: Top 28%
Photosynthetic Processes and Mechanisms
0.70
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