Pseudomonas aeruginosa elastase (LasB) as a therapeutic target

MJ Everett, DT Davies - Drug Discovery Today, 2021 - Elsevier
The Pseudomonas aeruginosa LasB elastase (elastase B, pseudolysin) is the predominant
protease in the P. aeruginosa secretome. It has been shown to hydrolyse a vast array of host …

[PDF][PDF] Angiotensin‐converting enzyme inhibitors: medicinal chemistry and biological actions

EW Petrillo Jr, MA Ondetti - Medicinal research reviews, 1982 - natmedlib.uz
The beginning of the 1980s may well be remembered as a turning point in the treatment of
hypertension, one of the most common of man's afflictions.'In 1980 and 1981, the first …

FK228 (depsipeptide) as a natural prodrug that inhibits class I histone deacetylases

R Furumai, A Matsuyama, N Kobashi, KH Lee… - Cancer research, 2002 - AACR
FK228 is a histone deacetylase (HDAC) inhibitor, the molecular mechanismof inhibition of
which has been unknown. Here we show that reduction of an intramolecular disulfide bond …

Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor

A Vannini, C Volpari, G Filocamo… - Proceedings of the …, 2004 - National Acad Sciences
Histone deacetylases (HDACs) are a family of enzymes involved in the regulation of gene
expression, DNA repair, and stress response. These processes often are altered in tumors …

Structural basis of the action of thermolysin and related zinc peptidases

BW Matthews - Accounts of Chemical research, 1988 - ACS Publications
Recent crystallographic and other studies havesuggested a detailed mechanism of action
for thermolysin, carboxypeptidase A, and related zinc endopeptidases. These studies also …

Phosphonamidates as transition-state analog inhibitors of thermolysin

PA Bartlett, CK Marlowe - Biochemistry, 1983 - ACS Publications
CaM binding protein discovered that actually has higher af-finity for CaM compared to CaM-
Ca2+„. We have avoided the temptation of naming P-57 more specifically until its function …

[图书][B] Mechanisms of protease action

L Polgar - 1989 - books.google.com
A uniform treatment of the four protease groups and a discussion of the differences and
similarities in their action is presented in this important new publication. Serine, cysteine …

Purification and substrate specificity of a strongly hydrophobic extracellular metalloendopeptidase (“gelatinase”) from Streptococcus faecalis (strain 0G1-10)

PL Mäkinen, DB Clewell, F An, KK Mäkinen - Journal of Biological …, 1989 - ASBMB
An extracellular Zn-endopeptidase was purified to homogeneity from the culture filtrates of
Streptococcus faecalis (human oral strain 0G1–10) by a procedure that comprised …

Multiple highly diverse structures complementary to enzyme binding sites: results of extensive application of a de novo design method incorporating combinatorial …

RS Bohacek, C McMartin - Journal of the American Chemical …, 1994 - ACS Publications
A computer program for de novo molecular design was used to explore thediversity of
molecules complementary to the binding sites of enzymes. The program, GrowMol* 1 …

Slow-and fast-binding inhibitors of thermolysin display different modes of binding: crystallographic analysis of extended phosphonamidate transition-state analogs

HM Holden, DE Tronrud, AF Monzingo, LH Weaver… - Biochemistry, 1987 - ACS Publications
Revised Manuscript Received August 6, 1987 abstract: The modes of binding to thermolysin
of two phosphonamidate peptide inhibitors, carbobenz-oxy-G/y'-L-Leu-L-Leu (ZGPLL) and …