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Mark A. Jarosinski

Researcher at Indiana University

Publications -  42
Citations -  4877

Mark A. Jarosinski is an academic researcher from Indiana University. The author has contributed to research in topics: Enantioselective synthesis & Receptor. The author has an hindex of 16, co-authored 40 publications receiving 4625 citations. Previous affiliations of Mark A. Jarosinski include University of Arizona & Amgen.

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Parkinson's Disease-associated α-Synuclein Is More Fibrillogenic than β- and γ-Synuclein and Cannot Cross-seed Its Homologs

TL;DR: β- and γ-synuclein are intrinsically less fibrillogenic than α- Synuclein and cannot form mixed fibrils with α- synuclein, which may explain why they do not appear in the pathological hallmarks of PD, although they are closely related to α-syn nuclein and are also abundant in brain.
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Structure of a human DNA repair protein UBA domain that interacts with HIV-1 Vpr.

TL;DR: The HIV-1 protein Vpr is critical for a number of viral functions including a unique ability to arrest T-cells at a G2/M checkpoint and induce subsequent apoptosis and it has been shown to interact specifically with the second UBA (ubiquitin associated) domain found in the DNA repair protein HHR23A, a highly evolutionarily conserved protein.
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Structural and conformational requirements for high-affinity binding to the SH2 domain of Grb2(1).

TL;DR: These stable and easily accessible cyclic peptides can serve as templates for the evaluation of phosphotyrosine surrogates and further chemical elaboration and the potency of the authors' cyclic lactams can be explained by the stabilization of the beta-turn conformation by three intramolecular hydrogen bonds.
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Diastereospecific tandem Michael-like addition / electrophilic bromination: A one-pot tandem asymmetric synthesis of precursors of unusual amino acids

TL;DR: In this paper, a series of key intermediates of unusual β-methyl-amino acids have been synthesized by using a modified Evans auxiliary in an asymmetric Michael-like reaction followed by direct bromination in a one-pot reaction.