AbstractThe turn of the millennium coincided with the branding of a fundamentally different class of enzyme - proteases that reside immersed inside the membrane. This new field was the convergence of completely separate lines of research focused on cholesterol homeostasis, Alzheimer's disease, and developmental genetics. None intended their ultimate path, but soon became a richly-integrated fabric for an entirely new field: regulated intramembrane proteolysis. Our aim in this Special Issue is to focus on the ancient and nearly ubiquitous enzymes that catalyze this unexpected yet important reaction. The pace of progress has been dramatic, resulting in a rapidly-expanding universe of known cellular functions, and a paradigm shift in the bioch...
The concept of proteases cleaving their substrates within the hydrophobic core of their transmembran...
Caspases are proteases at the heart of networks that govern apoptosis and inflammation. The past dec...
Recent studies demonstrate that presenilins (PSs) and signal peptide peptidase (SPP) are members of ...
Proteases carry out a wide variety of physiological functions. This review presents a brief history ...
Intramembrane proteases (IMPs) are localized within lipid bilayers of membranes-either the cell memb...
Intramembrane proteases are membrane enzymes whose active site is buried below the surface of the bi...
Proteases are considered attractive drug targets. Various drugs targeting classical, soluble proteas...
AbstractIntramembrane-cleaving proteases (I-CLiPs) are membrane embedded proteolytic enzymes. All su...
Intramembrane proteases (IMPs) reside inside lipid bilayers and perform peptide hydrolysis in transm...
AbstractIntramembrane-cleaving proteases are members of a novel type of enzyme that hydrolyse substr...
Intramembrane proteases have attracted much attention because of their biological and medical value....
Matrix metalloproteinases (MMPs), originally discovered to function in the breakdown of extracellula...
AbstractEndopeptidase classification based on catalytic mechanism and evolutionary history has prove...
Proteases can play key roles in regulation by controlling the levels of critical components of, for ...
Rhomboids were only discovered to be novel proteases in 2001, but progress on understanding this new...
The concept of proteases cleaving their substrates within the hydrophobic core of their transmembran...
Caspases are proteases at the heart of networks that govern apoptosis and inflammation. The past dec...
Recent studies demonstrate that presenilins (PSs) and signal peptide peptidase (SPP) are members of ...
Proteases carry out a wide variety of physiological functions. This review presents a brief history ...
Intramembrane proteases (IMPs) are localized within lipid bilayers of membranes-either the cell memb...
Intramembrane proteases are membrane enzymes whose active site is buried below the surface of the bi...
Proteases are considered attractive drug targets. Various drugs targeting classical, soluble proteas...
AbstractIntramembrane-cleaving proteases (I-CLiPs) are membrane embedded proteolytic enzymes. All su...
Intramembrane proteases (IMPs) reside inside lipid bilayers and perform peptide hydrolysis in transm...
AbstractIntramembrane-cleaving proteases are members of a novel type of enzyme that hydrolyse substr...
Intramembrane proteases have attracted much attention because of their biological and medical value....
Matrix metalloproteinases (MMPs), originally discovered to function in the breakdown of extracellula...
AbstractEndopeptidase classification based on catalytic mechanism and evolutionary history has prove...
Proteases can play key roles in regulation by controlling the levels of critical components of, for ...
Rhomboids were only discovered to be novel proteases in 2001, but progress on understanding this new...
The concept of proteases cleaving their substrates within the hydrophobic core of their transmembran...
Caspases are proteases at the heart of networks that govern apoptosis and inflammation. The past dec...
Recent studies demonstrate that presenilins (PSs) and signal peptide peptidase (SPP) are members of ...