Targeting key proteins involved in transcriptional regulation for cancer therapy: Current strategies and future prospective

H Pei, W Guo, Y Peng, H Xiong… - Medicinal Research …, 2022 - Wiley Online Library
The key proteins involved in transcriptional regulation play convergent roles in cellular
homeostasis, and their dysfunction mediates aberrant gene expressions that underline the …

Regulation of the structure and activity of pyruvate carboxylase by acetyl CoA

A Adina-Zada, TN Zeczycki, PV Attwood - Archives of biochemistry and …, 2012 - Elsevier
In this review we examine the effects of the allosteric activator, acetyl CoA on both the
structure and catalytic activities of pyruvate carboxylase. We describe how the binding of …

[HTML][HTML] Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I histone deacetylases

CJ Chou, D Herman, JM Gottesfeld - Journal of Biological Chemistry, 2008 - ASBMB
Histone deacetylase (HDAC) inhibitors, including various benzamides and hydroxamates,
are currently in clinical development for a broad range of human diseases, including cancer …

Potent slow-binding inhibition of cathepsin B by its propeptide

T Fox, E De Miguel, JS Mort, AC Storer - Biochemistry, 1992 - ACS Publications
Revised Manuscript Received October 8, 1992 abstract: A peptide (PCB1) corresponding to
the proregion of the rat cysteine protease cathepsin B was synthesized and its ability to …

Inhibition of aminopeptidases by amastatin and bestatin derivatives. Effect of inhibitor structure on slow-binding processes

DH Rich, BJ Moon, S Harbeson - Journal of medicinal chemistry, 1984 - ACS Publications
Amastatin [(2S, 3P)-3-amino-2-hydroxy-5-methylhexanoyl-L-valyl-L-valyl-L-aspartic acid]
and bestatin [(2S, 3fl)-3-amino-2-hydroxy-4-phenylbutanoyl-L-leucine] are slow-binding …

Regression analysis of nonlinear Arrhenius plots: an empirical model and a computer program

RG Duggleby - Computers in biology and medicine, 1984 - Elsevier
The rates of most physical, chemical and biological processes vary with temperature and
numerous instances have been reported in which Arrhenius plots of the experimental data …

Automated analysis of enzyme inactivation phenomena: application to β-lactamases and DD-peptidases

F De Meester, B Joris, G Reckinger… - Biochemical …, 1987 - Elsevier
In the presence of a reporter substrate, the progressive inactivation of an enzyme was easily
studied by directly transmitting absorbance readings to a microcomputer. Pseudo-first order …

Caloric restriction increases gluconeogenic and transaminase enzyme activities in mouse liver

K Hagopian, JJ Ramsey, R Weindruch - Experimental gerontology, 2003 - Elsevier
Long-term caloric restriction (CR) has been shown to extend maximum life span in
laboratory rodents. We investigated the activities of gluconeogenic and transaminase …

Novel, nonpeptidic cyanamides as potent and reversible inhibitors of human cathepsins K and L

JP Falgueyret, RM Oballa, O Okamoto… - Journal of medicinal …, 2001 - ACS Publications
Compounds containing a 1-cyanopyrrolidinyl ring were identified as potent and reversible
inhibitors of cathepsins K and L. The original lead compound 1 inhibits cathepsins K and L …

[HTML][HTML] Potent mechanism-based inhibitors for matrix metalloproteinases

M Ikejiri, MM Bernardo, RD Bonfil, M Toth… - Journal of Biological …, 2005 - ASBMB
Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that play important
roles in physiological and pathological conditions. Both gelatinases (MMP-2 and-9) and …