scholarly article | Q13442814 |
P50 | author | Morten P. Meldal | Q6914509 |
Jeremy C. Mottram | Q41417991 | ||
Jorge Arevalo | Q56483707 | ||
Phaedria M St Hilaire | Q114674245 | ||
P2093 | author name string | Graham H Coombs | |
Luiz Juliano | |||
Maria A Juliano | |||
Manat Renil | |||
Sanya J Sanderson | |||
Fatima Herrera | |||
Lira C Alves | |||
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The multiple cpb cysteine proteinase genes of Leishmania mexicana encode isoenzymes that differ in their stage regulation and substrate preferences | Q48049558 | ||
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Renin inhibitors containing isosteric replacements of the amide bond connecting the P3 and P2 sites | Q68927791 | ||
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Structure based development of novel specific inhibitors for cathepsin L and cathepsin S in vitro and in vivo | Q73077056 | ||
Mechanism of inhibition of cathepsin K by potent, selective 1, 5-diacylcarbohydrazides: a new class of mechanism-based inhibitors of thiol proteases | Q73334004 | ||
Structure of papain refined at 1.65 A resolution | Q27729147 | ||
Conformationally constrained 1,3-diamino ketones: a series of potent inhibitors of the cysteine protease cathepsin K | Q27765282 | ||
Use of papain as a model for the structure-based design of cathepsin K inhibitors: crystal structures of two papain-inhibitor complexes demonstrate binding to S'-subsites | Q27765850 | ||
Drug resistance in leishmaniasis: its implication in systemic chemotherapy of cutaneous and mucocutaneous disease | Q28326560 | ||
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Potent, low-molecular-weight non-peptide inhibitors of malarial aspartyl protease plasmepsin II. | Q30672366 | ||
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Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery | Q33267847 | ||
Multiple high activity cysteine proteases of Leishmania mexicana are encoded by the Imcpb gene array | Q34341002 | ||
Cysteine protease inhibitors as chemotherapy: lessons from a parasite target | Q36176812 | ||
BIA/MS: interfacing biomolecular interaction analysis with mass spectrometry | Q36845637 | ||
Leishmania major: molecular modeling of cysteine proteases and prediction of new nonpeptide inhibitors | Q36891348 | ||
??? | Q27629293 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Leishmania mexicana | Q2493771 |
P304 | page(s) | 1971-1982 | |
P577 | publication date | 2002-05-01 | |
P1433 | published in | Journal of Medicinal Chemistry | Q900316 |
P1476 | title | Solid-phase library synthesis, screening, and selection of tight-binding reduced peptide bond inhibitors of a recombinant Leishmania mexicana cysteine protease B. | |
P478 | volume | 45 |
Q33202737 | Combinatorial library of peptidotriazoles: identification of [1,2,3]-triazole inhibitors against a recombinant Leishmania mexicana cysteine protease |
Q44949896 | Cyclic, linear, cycloretro-isomer, and cycloretro-inverso peptides derived from the C-terminal sequence of bradykinin as substrates or inhibitors of serine and cysteine proteases |
Q40517959 | Differences in substrate specificities between cysteine protease CPB isoforms of Leishmania mexicana are mediated by a few amino acid changes |
Q35053473 | Heparin modulates the endopeptidase activity of Leishmania mexicana cysteine protease cathepsin L-Like rCPB2.8. |
Q36288119 | Highly sensitive and adaptable fluorescence-quenched pair discloses the substrate specificity profiles in diverse protease families |
Q37947476 | Microwave heating in solid-phase peptide synthesis |
Q36033291 | Peptides and Peptide Analogs to Inhibit Protein-Protein Interactions |
Q37708228 | Ralph F. Hirschmann award address 2009: Merger of organic chemistry with peptide diversity. |
Q37780442 | Solid-phase synthesis of N-substituted glycine oligomers (alpha-peptoids) and derivatives. |
Q33355343 | Synthesis, screening, and sequencing of cysteine-rich one-bead one-compound peptide libraries |
Q33184660 | The one-bead two-compound assay for solid phase screening of combinatorial libraries |
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