A new phospholipase A2 (PLA2)-inhibitory protein was isolated from the plasma of Atropoides nummifer, a crotaline snake from Central America. This inhibitor was named AnMIP, given its ability to neutralize the activity of basic PLA2 myotoxins of its own and related venoms. The cDNA of AnMIP was cloned and sequenced, showing that it belongs to the α group of phospholipase A2 inhibitors (PLIs). AnMIP appears as a homotrimer in the native state, held together by non-covalent forces, with a subunit molecular mass of 22,247–22,301 and an isoelectric point of 4.1–4.7. This trimeric structure is the first observed in a PLIα from American crotaline snakes, previously reported only in Asian species. Sequencing, mass spectrometry, and analytical...
Venomous and non-venomous snakes possess phospholipase A(2) (PLA(2)) inhibitory proteins (PLIs) in t...
Bothrops mattogrossensis snake is widely distributed throughout eastern South America and is respons...
A basic protein was isolated by CM-Sephadex C-25 chromatography from the venom of Bothrops neuwiedii...
Phospholipases A(2) (PLA(2)s) are important components of Bothrops snake venoms, that can induce sev...
Phospholipases A(2) (PLA(2)s) are important components of Bothrops snake venoms, that can induce sev...
Phospholipases A(2) (PLA(2)s) are important components of Bothrops snake venoms, that can induce sev...
Myotoxic phospholipases A2 (PLA2s; group II) account for most of the muscle-tissue damage that resul...
AbstractPhospholipases A2 (PLA2s) are important components of Bothrops snake venoms, that can induce...
Myotoxic phospholipases A2 of class II are commonly found in the venoms of crotalid snakes. As an ap...
Phospholipases A2 (PLA2) are enzymes acting on the cell membrane phospholipids resulting in fatty ac...
Abstract The blood plasma of numerous snake species naturally comprises endogenous phospholipase A2 ...
AbstractThis paper reports the biochemical and pharmacological characterization of a new myotoxic PL...
Phospholipases A2inhibitors (PLIs) produced by venomous and non-venomous snakes play essentialrole i...
In 1984, the first venom phospholipase A2 (PLA2) with a lysine substituting for the highly conserved...
<div><p>Phospholipases A<sub>2</sub> (PLA<sub>2</sub>) are enzymes acting on the cell membrane phosp...
Venomous and non-venomous snakes possess phospholipase A(2) (PLA(2)) inhibitory proteins (PLIs) in t...
Bothrops mattogrossensis snake is widely distributed throughout eastern South America and is respons...
A basic protein was isolated by CM-Sephadex C-25 chromatography from the venom of Bothrops neuwiedii...
Phospholipases A(2) (PLA(2)s) are important components of Bothrops snake venoms, that can induce sev...
Phospholipases A(2) (PLA(2)s) are important components of Bothrops snake venoms, that can induce sev...
Phospholipases A(2) (PLA(2)s) are important components of Bothrops snake venoms, that can induce sev...
Myotoxic phospholipases A2 (PLA2s; group II) account for most of the muscle-tissue damage that resul...
AbstractPhospholipases A2 (PLA2s) are important components of Bothrops snake venoms, that can induce...
Myotoxic phospholipases A2 of class II are commonly found in the venoms of crotalid snakes. As an ap...
Phospholipases A2 (PLA2) are enzymes acting on the cell membrane phospholipids resulting in fatty ac...
Abstract The blood plasma of numerous snake species naturally comprises endogenous phospholipase A2 ...
AbstractThis paper reports the biochemical and pharmacological characterization of a new myotoxic PL...
Phospholipases A2inhibitors (PLIs) produced by venomous and non-venomous snakes play essentialrole i...
In 1984, the first venom phospholipase A2 (PLA2) with a lysine substituting for the highly conserved...
<div><p>Phospholipases A<sub>2</sub> (PLA<sub>2</sub>) are enzymes acting on the cell membrane phosp...
Venomous and non-venomous snakes possess phospholipase A(2) (PLA(2)) inhibitory proteins (PLIs) in t...
Bothrops mattogrossensis snake is widely distributed throughout eastern South America and is respons...
A basic protein was isolated by CM-Sephadex C-25 chromatography from the venom of Bothrops neuwiedii...