Author

M. K. Borah

Indian Institute of Technology JammuORCID 0009-0002-4553-7306Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Pharmacology & Toxicology· 1

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:protein structure prediction· 1 Assay:proteomics· 1

Frequent Co-Authors

Mahek Agrawal· 1 shared Mithu BaidyaiD· 1 shared Neeraj SoniiD· 1 shared Punita KumariiD· 1 shared Sarfraz Ahmed· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

5 top collaborators · 10 mutual co-author links

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1 shared paperPharmacology & Toxicology

Mahek Agrawal

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1 paper

Recent·Most cited

Sparse Phosphorylatable Residues, Tuned by Agonist Chemotype, Shapes GPCR Signaling

M. K. Borah, Sarfraz Ahmed, Mahek Agrawal, Neeraj Soni, Punita Kumari, Mithu Baidya

This study shows that GPCR signaling diversity can arise from a sparse set of phosphorylation sites rather than an extensive barcode, with ligand chemotype influencing their functional impact.

bioRxiv · Oct 14, 2026 · PreprintPharmacology & Toxicology