<div><p>Protein carbamylation is a post-translational modification that can occur in the presence of urea. In solution, urea is in equilibrium with ammonium cyanate, and carbamylation occurs when cyanate ions react with the amino groups of lysines, arginines, protein N-termini, as well as sulfhydryl groups of cysteines. The concentration of urea is elevated in the renal inner medulla compared with other tissues. Due to the high urea concentration, we hypothesized that carbamylation can occur endogenously within the rat inner medulla. Using immunoblotting of rat kidney cortical and medullary homogenates with a carbamyl-lysine specific antibody, we showed that carbamylation is present in a large number of inner medullary proteins. Using prote...
Carbamoylation of glomerular and tubular proteins in patients with kidney failure
Protein carbamylation by cyanate is a post-translational modification associated with several (patho...
International audienceTissue aging is a complex phenomenon involving molecular aging of matrix prote...
Protein carbamylation is a post-translational modification that can occur in the presence of urea. I...
Carbamoylation of amino acids and proteins in uremia. Cyanate spontaneously transformed from urea in...
La réaction de carbamylation, comme les réactions de glycation, d’oxydation ou de carbonylation, fai...
Spontaneous urea dissociation in water solution is a prominent source of protein carbamylation in ou...
SummaryCarbamylation by urea-derived cyanate is a posttranslational modification of proteins increas...
Cyanate exists in equilibrium with urea and in its reactive form, isocyanic acid, forms a stable add...
<p>The carbamylation sites identified are based on pooled mass spectrometry data of carbamyl sites i...
Les modifications post-traductionnelles non enzymatiques des protéines, comme la glycation, l'oxydat...
Protein carbamoylation is a non-enzymatic post-translational modification that binds isocyanic acid,...
AbstractCarbamylation is a post-translational modification of proteins characterized by the binding ...
Carbamylation is widely quoted as being a problem in 2-D gel analysis and the associated sample prep...
Changes in protein and mRNAs for enzymes of glutamine metabolism were determined in rat kidney corte...
Carbamoylation of glomerular and tubular proteins in patients with kidney failure
Protein carbamylation by cyanate is a post-translational modification associated with several (patho...
International audienceTissue aging is a complex phenomenon involving molecular aging of matrix prote...
Protein carbamylation is a post-translational modification that can occur in the presence of urea. I...
Carbamoylation of amino acids and proteins in uremia. Cyanate spontaneously transformed from urea in...
La réaction de carbamylation, comme les réactions de glycation, d’oxydation ou de carbonylation, fai...
Spontaneous urea dissociation in water solution is a prominent source of protein carbamylation in ou...
SummaryCarbamylation by urea-derived cyanate is a posttranslational modification of proteins increas...
Cyanate exists in equilibrium with urea and in its reactive form, isocyanic acid, forms a stable add...
<p>The carbamylation sites identified are based on pooled mass spectrometry data of carbamyl sites i...
Les modifications post-traductionnelles non enzymatiques des protéines, comme la glycation, l'oxydat...
Protein carbamoylation is a non-enzymatic post-translational modification that binds isocyanic acid,...
AbstractCarbamylation is a post-translational modification of proteins characterized by the binding ...
Carbamylation is widely quoted as being a problem in 2-D gel analysis and the associated sample prep...
Changes in protein and mRNAs for enzymes of glutamine metabolism were determined in rat kidney corte...
Carbamoylation of glomerular and tubular proteins in patients with kidney failure
Protein carbamylation by cyanate is a post-translational modification associated with several (patho...
International audienceTissue aging is a complex phenomenon involving molecular aging of matrix prote...