Arun K. Shukla
Affiliations: | Duke University, Durham, NC |
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"Arun Shukla"Mean distance: 106866
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Publications
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Maharana J, Sano FK, Sarma P, et al. (2024) Molecular insights into atypical modes of β-arrestin interaction with seven transmembrane receptors. Science (New York, N.Y.). 383: 101-108 |
Yadav MK, Maharana J, Yadav R, et al. (2023) Molecular basis of anaphylatoxin binding, activation, and signaling bias at complement receptors. Cell |
Sarma P, Carino CMC, Seetharama D, et al. (2023) Molecular insights into intrinsic transducer-coupling bias in the CXCR4-CXCR7 system. Nature Communications. 14: 4808 |
Isaikina P, Petrovic I, Jakob RP, et al. (2023) A key GPCR phosphorylation motif discovered in arrestin2⋅CCR5 phosphopeptide complexes. Molecular Cell |
Maharana J, Sarma P, Yadav MK, et al. (2023) Structural snapshots uncover a key phosphorylation motif in GPCRs driving β-arrestin activation. Molecular Cell |
Grimes J, Koszegi Z, Lanoiselée Y, et al. (2023) Plasma membrane preassociation drives β-arrestin coupling to receptors and activation. Cell. 186: 2238-2255.e20 |
Sarma P, Shukla AK. (2022) Resonating with the signaling bias of CXCR7. Molecular Cell. 82: 3318-3320 |
Sarma P, Banerjee R, Shukla AK. (2022) Structural snapshot of a β-arrestin-biased receptor. Trends in Pharmacological Sciences |
Baidya M, Chaturvedi M, Dwivedi-Agnihotri H, et al. (2022) Allosteric modulation of GPCR-induced β-arrestin trafficking and signaling by a synthetic intrabody. Nature Communications. 13: 4634 |
Maharana J, Banerjee R, Yadav MK, et al. (2022) Emerging structural insights into GPCR-β-arrestin interaction and functional outcomes. Current Opinion in Structural Biology. 75: 102406 |