Introduction of α-hydroxymethyamino acid residues in substrate specificity P1 position of trypsin inhibitor SFTI-1 from sunflower seeds retains its activity

Biochemical and Biophysical Research Communications

Volumn 340, Issue 3, 2006, Pages 823-828

  Zabłotna, Ewa ^a   Kret, Agnieszka ^a   Jaśkiewicz, Anna ^a   Olma, Aleksandra ^b   Leplawy, Mirosław T ^b   Rolka, Krzysztof ^a  

^a UNIVERSITY OF GDA SK   (Poland)

^b LODZ UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

Hydroxymethylamino acids; Elastase; Inhibitors; Peptides; Trypsin

Indexed keywords

LEUKOCYTE ELASTASE; TRYPSIN INHIBITOR;

ARTICLE; ELECTRICITY; ENZYME SPECIFICITY; EQUILIBRIUM CONSTANT; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; SUNFLOWER; SYNTHESIS;

AMINO ACID SEQUENCE; AMINO ACIDS; ANIMALS; ASPARTIC ACID; BINDING SITES; CATTLE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ELECTROSTATICS; ENZYME INHIBITORS; HELIANTHUS; HUMANS; KINETICS; LEUKOCYTE ELASTASE; MODELS, CHEMICAL; MOLECULAR SEQUENCE DATA; PEPTIDES; PEPTIDES, CYCLIC; PROTEIN STRUCTURE, TERTIARY; SEEDS; SERINE; SERINE ENDOPEPTIDASES; SERINE PROTEINASE INHIBITORS; STEREOISOMERISM; SUBSTRATE SPECIFICITY; TRYPSIN; TRYPSIN INHIBITORS;

BOVINAE; HELIANTHUS;

EID: 30144434911     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2005.12.074     Document Type: Article

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