Published in Chembiochem on June 01, 2005
Investigation of the substrate specificity of lacticin 481 synthetase by using nonproteinogenic amino acids. Chembiochem (2009) 1.02
Metabolism of peptide reporters in cell lysates and single cells. Analyst (2012) 1.00
Facile synthesis of native and protease-resistant ubiquitylated peptides. Chembiochem (2014) 0.81
Cross-linked peptoid-based dimerization inhibitors of HIV-1 protease. Chembiochem (2010) 0.81
Collagenolytic Matrix Metalloproteinase Activities toward Peptomeric Triple-Helical Substrates. Biochemistry (2015) 0.76
Synthesis of acylhydrazino-peptomers, a new class of peptidomimetics, by consecutive Ugi and hydrazino-Ugi reactions. Beilstein J Org Chem (2016) 0.75
High throughput screening of potentially selective MMP-13 exosite inhibitors utilizing a triple-helical FRET substrate. Bioorg Med Chem (2008) 1.03
Effects of cyclic lipodepsipeptide structural modulation on stability, antibacterial activity, and human cell toxicity. ChemMedChem (2012) 0.98
Nociceptin inhibits acquisition of amphetamine-induced place preference and sensitization to stereotypy in rats. Eur J Pharmacol (2003) 0.96
Antifungal action of human cathelicidin fragment (LL13-37) on Candida albicans. Peptides (2011) 0.91
Effects of cathelicidin and its fragments on three key enzymes of HIV-1. Peptides (2011) 0.89
In vitro and in vivo analyses of the biological activity of RGD peptides towards Ab Bomirski melanoma. Cell Mol Biol Lett (2003) 0.86
The dimeric and tetrameric octarepeat fragments of prion protein behave differently to its monomeric unit. Dalton Trans (2004) 0.86
Sunflower trypsin inhibitor 1 as a molecular scaffold for drug discovery. Curr Pharm Des (2011) 0.85
Design of selective substrates of proteinase 3 using combinatorial chemistry methods. Anal Biochem (2008) 0.83
New chromogenic substrates of human neutrophil cathepsin G containing non-natural aromatic amino acid residues in position P(1) selected by combinatorial chemistry methods. Mol Divers (2007) 0.83
Screening of environmental samples for bacteria producing 1,3-propanediol from glycerol. Acta Biochim Pol (2012) 0.83
Introduction of alpha-hydroxymethyamino acid residues in substrate specificity P1 position of trypsin inhibitor SFTI-1 from sunflower seeds retains its activity. Biochem Biophys Res Commun (2005) 0.83
Design of serine proteinase inhibitors by combinatorial chemistry using trypsin inhibitor SFTI-1 as a starting structure. J Pept Sci (2007) 0.82
Trypsin inhibitors from the garden four o'clock (Mirabilis jalapa) and spinach (Spinacia oleracea) seeds: isolation, characterization and chemical synthesis. Phytochemistry (2007) 0.81
Implication of the disulfide bridge in trypsin inhibitor SFTI-1 in its interaction with serine proteinases. Bioorg Med Chem (2010) 0.81
The new fluorogenic substrates of neutrophil proteinase 3 optimized in prime site region. Anal Biochem (2010) 0.80
Selenopeptide analogs of EETI-II retain potent trypsin inhibitory activities. Chem Biol Drug Des (2010) 0.79
Fluorescent analogs of trypsin inhibitor SFTI-1 isolated from sunflower seeds-synthesis and applications. Biopolymers (2014) 0.78
Inhibitory and antimicrobial activities of OGTI and HV-BBI peptides, fragments and analogs derived from amphibian skin. Peptides (2012) 0.78
Chemical synthesis and kinetic study of the smallest naturally occurring trypsin inhibitor SFTI-1 isolated from sunflower seeds and its analogues. Biochem Biophys Res Commun (2002) 0.78
Substrate specificity of Staphylococcus aureus cysteine proteases--Staphopains A, B and C. Biochimie (2011) 0.78
Atomic resolution crystal structure of HV-BBI protease inhibitor from amphibian skin in complex with bovine trypsin. Proteins (2015) 0.78
Three wavelength substrate system of neutrophil serine proteinases. Anal Chem (2012) 0.78
Structural and dynamic characterization of copper(II) binding of the human prion protein outside the octarepeat region. Chemistry (2007) 0.78
New potent cathepsin G phosphonate inhibitors. Bioorg Med Chem (2008) 0.77
Designing of substrates and inhibitors of bovine alpha-chymotrypsin with synthetic phenylalanine analogues in position P(1). Protein Pept Lett (2008) 0.77
Development of sensitive cathepsin G fluorogenic substrate using combinatorial chemistry methods. Anal Biochem (2008) 0.77
Analogues of trypsin inhibitor SFTI-1 with disulfide bridge substituted by various length of carbonyl bridges. Protein Pept Lett (2010) 0.77
A practical synthesis of N α-Fmoc protected L-threo-β-hydroxyaspartic acid derivatives for coupling via α- or β-carboxylic group. Amino Acids (2010) 0.76
Selection of new chromogenic substrates of serine proteinases using combinatorial chemistry methods. Comb Chem High Throughput Screen (2007) 0.76
Inhibitory activity of double-sequence analogues of trypsin inhibitor SFTI-1 from sunflower seeds: an example of peptide splicing. FEBS J (2010) 0.76
Biochemical and structural characterization of SplD protease from Staphylococcus aureus. PLoS One (2013) 0.76
Introduction of non-natural amino acid residues into the substrate-specific P1 position of trypsin inhibitor SFTI-1 yields potent chymotrypsin and cathepsin G inhibitors. Bioorg Med Chem (2009) 0.76
Introduction of Pro and its analogues in the conserved P1' position of trypsin inhibitor SFTI-1 retains its inhibitory activity. Protein Pept Lett (2011) 0.76
Matrix metalloproteinase inhibition by heterotrimeric triple-helical Peptide transition state analogues. Chembiochem (2015) 0.75
Identification of bikunin as an endogenous inhibitor of dynorphin convertase in human cerebrospinal fluid. FEBS J (2006) 0.75
Expanding chemical diversity of conotoxins: peptoid-peptide chimeras of the sodium channel blocker μ-KIIIA and its selenopeptide analogues. Eur J Med Chem (2013) 0.75
Pegylated fluorescent peptides as substrates of proteolytic enzymes. Protein Pept Lett (2012) 0.75
A simple method for selection of trypsin chromogenic substrates using combinatorial chemistry approach. Biochem Biophys Res Commun (2004) 0.75
Highly specific substrates of proteinase 3 containing 3-(2-benzoxazol-5-yl)-l-alanine and their application for detection of this enzyme in human serum. Anal Chem (2010) 0.75
Conformational solution studies of neuropeptide gamma using CD and NMR spectroscopy. J Pept Sci (2002) 0.75
1,3-propanediol production by Escherichia coli expressing genes of dha operon from Clostridium butyricum 2CR371.5. Acta Biochim Pol (2012) 0.75
Peptomeric analogues of trypsin inhibitor SFTI-1 isolated from sunflower seeds. Bioorg Med Chem (2008) 0.75
The antifungal properties of chicken egg cystatin against Candida yeast isolates showing different levels of azole resistance. Mycoses (2009) 0.75
Rat neuronal cells in primary culture as a model for nociceptin/orphanin FQ metabolism. Neurosci Lett (2003) 0.75
Selection of low-molecular-mass trypsin and chymotrypsin inhibitors based on the binding loop of CMTI-III using combinatorial chemistry methods. Biochem Biophys Res Commun (2003) 0.75
Conformational studies of [Abu(3, 11)]-SFTI-1, an analogue of the trypsin inhibitor isolated from sunflower seeds. J Pept Sci (2008) 0.75
The prion peptide forms ion channels in planar lipid bilayers. Cell Mol Biol Lett (2003) 0.75
Selection of peptomeric inhibitors of bovine alpha-chymotrypsin and cathepsin G based on trypsin inhibitor SFTI-1 using a combinatorial chemistry approach. Mol Divers (2009) 0.75
The influence of substrate peptide length on human beta-tryptase specificity. J Pept Sci (2008) 0.75
Activities of Venom Proteins and Peptides with Possible Therapeutic Applications from Bees and WASPS. Protein Pept Lett (2016) 0.75
Investigation of peptide splicing using two-peptide-chain analogs of trypsin inhibitor SFTI-1. FEBS J (2013) 0.75
Low-molecular-weight aldehyde inhibitors of cathepsin G. Protein Pept Lett (2009) 0.75