serine and 4-nitrophenyl acetate

serine has been researched along with 4-nitrophenyl acetate in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Trudelle, Y1
Ansari, GA; Kaphalia, BS; Mericle, KA1
Bugg, TD; Li, JJ1
Chen, Z; Jiang, W; Liu, X; Shu, J; Xu, B; Xu, Z; Yue, J; Zhang, Q; Zhang, Y1

Other Studies

4 other study(ies) available for serine and 4-nitrophenyl acetate

ArticleYear
Synthesis, conformation and reactivity towards p-nitrophenyl acetate of polypeptides incorporating aspartic acid, serine and histidine.
    International journal of peptide and protein research, 1982, Volume: 19, Issue:5

    Topics: Amino Acid Sequence; Aspartic Acid; Binding Sites; Chymotrypsin; Circular Dichroism; Histidine; Nitrophenols; Peptides; Protein Conformation; Serine; Spectrophotometry, Infrared; Structure-Activity Relationship; Subtilisins

1982
Mechanism of differential inhibition of hepatic and pancreatic fatty acid ethyl ester synthase by inhibitors of serine-esterases: in vitro and cell culture studies.
    Toxicology and applied pharmacology, 2004, Oct-01, Volume: 200, Issue:1

    Topics: Acyltransferases; Animals; Carboxylesterase; Cell Line, Tumor; Cholinesterases; Esterases; Humans; Indicators and Reagents; Liver; Microdialysis; Nitrophenols; Organophosphorus Compounds; Pancreas; Pyrones; Serine; Substrate Specificity; Swine

2004
Investigation of a general base mechanism for ester hydrolysis in C-C hydrolase enzymes of the alpha/beta-hydrolase superfamily: a novel mechanism for the serine catalytic triad.
    Organic & biomolecular chemistry, 2007, Feb-07, Volume: 5, Issue:3

    Topics: Benzoates; Binding Sites; Burkholderia; Catalysis; Escherichia coli; Escherichia coli Proteins; Esterases; Esters; Hydrogen-Ion Concentration; Hydrolases; Hydrolysis; Kinetics; Lipase; Nitrophenols; Serine; Substrate Specificity

2007
Structures and esterolytic reactivity of novel binuclear copper(ii) complexes with reduced l-serine Schiff bases as mimic carboxylesterases.
    Dalton transactions (Cambridge, England : 2003), 2020, Aug-07, Volume: 49, Issue:29

    Topics: Biomimetic Materials; Carboxylic Ester Hydrolases; Coordination Complexes; Copper; Density Functional Theory; Esters; Hydrolysis; Models, Molecular; Molecular Structure; Nitrophenols; Oxidation-Reduction; Schiff Bases; Serine

2020