Results 271 to 280 of about 358,313 (362)

Degradation of Nonribosomal Peptide Synthetase Megasynthetases SrfAA and SrfAB by Acyldepsipeptide‐Activated ClpP in Bacillus Subtilis

open access: yesChemBioChem, EarlyView.
FtsZ is the only target protein that has been biochemically confirmed to be hydrolyzed both in vitro and in bacterial cells. Coupled with activity‐based protein profiling of nonribosomal peptide synthetases, the ClpP‐ADEP1 proteolytic complex that degrades the surfactin synthetases SrfAA and SrfAB in cell lysates and bacterial cells is demonstrated ...
Fumihiro Ishikawa   +4 more
wiley   +1 more source

Neutrophils from patients with acquired neutropenia exhibit alterations in serine protease immunostaining and activity. [PDF]

open access: yesBr J Haematol
Mazur A   +6 more
europepmc   +1 more source

Profiling Serine Hydrolases in the Leishmania Host‐Pathogen Interactome Using Cell‐Permeable Activity‐Based Fluorophosphonate Probes

open access: yesChemBioChem, Accepted Article.
Leishmaniasis, a vector borne neglected tropical disease, caused by the protozoan parasite Leishmania, is a major global public health challenge with millions of new cases annually. Treatment of leishmaniasis is difficult for many reasons including a multiple life‐cycle stages, involving both an infective insect vector form, the promastigote, and a ...
Jaime A. Isern   +7 more
wiley   +1 more source

Microsporidian Nosema bombycis secretes serine protease inhibitor to suppress host cell apoptosis via Caspase BmICE. [PDF]

open access: yesPLoS Pathog
Ran M   +12 more
europepmc   +1 more source

The sequence and reactive site of ecotin. A general inhibitor of pancreatic serine proteases from Escherichia coli.

open access: hybrid, 1991
Marisa E. McGrath   +4 more
openalex   +1 more source

Design and Evaluation of Bivalent K‐Ras Inhibitors That Target the CAAX Binding Site and the Acidic Surface of Farnesyltransferase and Geranylgeranyltransferase I

open access: yesChemistry – A European Journal, EarlyView.
Chemical inhibition of K‐Ras posttranslational prenylation represents a promising strategy against aggressive cancers. A structure‐based design produces piperidine‐based peptidomimetics conjugated to cationic modules, effectively inhibiting FTase and GGTase I at single‐digit nanomolar concentrations.
Naomi Horiuchi   +8 more
wiley   +1 more source

Identification of the interaction between MAPK1 and Eimeria acervulina serine protease inhibitor: a preliminary functional study. [PDF]

open access: yesActa Biochim Biophys Sin (Shanghai)
Lian L   +9 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy