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Sankaran Krishnaswamy

Researcher at Madurai Kamaraj University

Publications -  49
Citations -  1970

Sankaran Krishnaswamy is an academic researcher from Madurai Kamaraj University. The author has contributed to research in topics: Porin & Prophage. The author has an hindex of 19, co-authored 49 publications receiving 1914 citations. Previous affiliations of Sankaran Krishnaswamy include Centre national de la recherche scientifique & Purdue University.

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Class II aminoacyl transfer RNA synthetases: crystal structure of yeast aspartyl-tRNA synthetase complexed with tRNA(Asp)

TL;DR: The crystal structure of the binary complex tRNA(Asp)-aspartyl tRNA synthetase from yeast was solved with the use of multiple isomorphous replacement to 3 angstrom resolution.
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Atomic structure of single-stranded DNA bacteriophage ΦX174 and its functional implications

TL;DR: The mechanism of DNA ejection, viral assembly and evolution are related to the structure of bacteriophage ΦX174, a T = 1 capsid whose major folding motif is the eight–stranded antiparallelβ barrel found in many other icosahedral viruses.
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Structural analysis of a series of antiviral agents complexed with human rhinovirus 14

TL;DR: Crystallographic studies of one of these mutants confirm the partial sequencing data and support the finding that this is a single mutation that occurs within the binding pocket, and are consistent with their observed antiviral activities against human rhinovirus 14 drug-resistant mutants and other rhinOVirus serotypes.
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C—H⋯O Hydrogen Bonds in β‐sheets

TL;DR: A detailed analysis of the occurrence of the C-H...O hydrogen bonds in sheet regions of proteins has been presented and an inverse correlation is observed between the hydrogen-bond geometries involving the C(alpha)(i)-h...O=C and the N(i+1)-H...
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Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)

TL;DR: This is the first study demonstrating that the p.Cys134Trp mutant does not have a strong impact on FOXL2 localization, solubility, and transactivation abilities on a panel of proven target promoters, behaving neither as a dominant-negative nor as a loss-of-function mutation.