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Biochimica Et Biophysica Acta. Biomembranes|March 16, 2020
Influence of disulfide bonds in human beta defensin-3 on its strain specific activity against Gram-negative bacteriaChristian Nehls, Arne Böhling, Rainer Podschun, et al.
Journal of Medicinal Chemistry|September 1, 2009
On-bead screening of a combinatorial fumaric acid derived peptide library yields antiplasmodial cysteine protease inhibitors with unusual peptide sequencesUwe Machon, Christian Büchold, Martin Stempka, et al.
Chemmedchem|August 26, 2006
Aziridide-based inhibitors of cathepsin L: synthesis, inhibition activity, and docking studiesRadim Vicik, Matthias Busemann, Christoph Gelhaus, et al.
Frontiers in Microbiology|August 24, 2019
The Inducible Response of the Nematode Caenorhabditis elegans to Members of Its Natural Microbiota Across Development and Adult LifeWentao Yang, Carola Petersen, Barbara Pees, et al.
Protein Expression and Purification|July 4, 2009
Cell-free synthesis and combinatorial selective 15N-labeling of the cytotoxic protein amoebapore A from Entamoeba histolyticaYang Xun, Pierre Tremouilhac, Colm Carraher, et al.
The Journal of Biological Chemistry|March 8, 2012
Macin family of antimicrobial proteins combines antimicrobial and nerve repair activitiesSascha Jung, Frank D Sönnichsen, Chien-Wen Hung, et al.
Molecules (Basel, Switzerland)|December 24, 2008
Synthesis and evaluation of non-peptidic cysteine protease inhibitors of P. falciparum derived from etacrynic acidMarie-Adrienne Dude, Ulrich Kaeppler, Monika Herb, et al.
Structure (London, England : 1993)|July 24, 2012
Structures of lysenin reveal a shared evolutionary origin for pore-forming proteins and its mode of sphingomyelin recognitionLuigi De Colibus, Andreas F-P Sonnen, Keith J Morris, et al.
The ISME Journal|September 6, 2019
The functional repertoire contained within the native microbiota of the model nematode Caenorhabditis elegansJohannes Zimmermann, Nancy Obeng, Wentao Yang, et al.
Chemistry & Biology|September 25, 2012
The natural anticancer compounds rocaglamides inhibit the Raf-MEK-ERK pathway by targeting prohibitin 1 and 2Gernot Polier, Jennifer Neumann, Frédéric Thuaud, et al.
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