Author

K. W. Tripp

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biophysics· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:protein sequence· 2 Research Focus:cell signaling & trafficking· 1 Organism:Drosophila· 1 Research Focus:protein design· 1 Research Focus:protein folding & dynamics· 1 Approach:statistical model· 1

Frequent Co-Authors

D. Barrick· 2 shared M. Sternke· 2 shared J. M. Kavran· 1 shared K. A. Weingartner· 1 shared T. Tran· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

5 top collaborators · 4 mutual co-author links

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2 shared papersBiophysics

D. Barrick

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3 papers

Recent·Most cited

Dimerization and autophosphorylation of the MST family of kinases are controlled by the same set of residues

J. M. Kavran, K. A. Weingartner, T. Tran, K. W. Tripp

This study identifies a shared dimerization interface in MST kinases that is essential for trans-autophosphorylation and activation across species.

bioRxiv · Mar 9, 2023 · PreprintBiochemistry

Surface residues and non-additive interactions stabilize a consensus homeodomain protein

M. Sternke, K. W. Tripp, D. Barrick

The paper investigates how substitutions in a consensus homeodomain protein contribute to its stabilization, finding that surface residues and charge-conserving substitutions play key roles.

bioRxiv · Apr 19, 2021Biophysics

Consensus sequence design as a general strategy to create hyperstable, biologically active proteins

M. Sternke, K. W. Tripp, D. Barrick

This study evaluates consensus sequence design for creating stable, biologically active proteins across six families, finding high success rates in stability and function.

bioRxiv · Apr 29, 2019Biophysics