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Jill E. Gready

Researcher at Australian National University

Publications -  100
Citations -  5146

Jill E. Gready is an academic researcher from Australian National University. The author has contributed to research in topics: Dihydrofolate reductase & Bond order. The author has an hindex of 32, co-authored 100 publications receiving 4712 citations. Previous affiliations of Jill E. Gready include University of Sydney.

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The C-type lectin-like domain superfamily

TL;DR: The superfamily of proteins containing C‐type lectin‐like domains (CTLDs) is a large group of extracellular Metazoan proteins with diverse functions that have evolved to specifically recognize protein, lipid and inorganic ligands, including the vertebrate clade‐specific snake venoms, and fish antifreeze and bird egg‐shell proteins.
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Green Evolution and Dynamic Adaptations Revealed by Genomes of the Marine Picoeukaryotes Micromonas

TL;DR: It is found that genomes from two isolates shared only 90% of their predicted genes, and divergence appears to have been facilitated by selection and acquisition processes that actively shape the repertoire of genes that are mutually exclusive between the two isolate differently than the core genes.
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Combining docking and molecular dynamic simulations in drug design.

TL;DR: This review focuses on applications and protocols of recent studies where docking calculations and molecular dynamics simulations were combined to dock small molecules into protein receptors, and is structured to lead the reader from the simpler to more compute‐intensive methods.
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Optimization of parameters for molecular dynamics simulation using smooth particle‐mesh Ewald in GROMACS 4.5

TL;DR: This tool will stimulate future work to assess the impact of the quality of the PME approximation on simulation outcomes, particularly with regard to the trade‐off between cost and scientific reliability in biomolecular applications.
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Identification of active site residues of the pro-metastatic endoglycosidase heparanase

TL;DR: Analysis of sequence alignments and secondary structure predictions suggest that heparanase is a member of the clan A glycosyl hydrolases and has a common catalytic mechanism that involves two conserved acidic residues, a putative proton donor at Glu(225) and a nucleophile at GLU(343).