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Dietary Nitrogen
Term | Definition |
---|---|
In the fed state, the liver can convert amino acid carbons to | fatty acids and glycerol, which form the triacylglycerols of very low density lipoprotein (VLDL). |
During fasting, muscle protein is degraded and supplies amino acids to the blood, and the liver converts amino acid carbons to | glucose or ketone bodies. |
Amino acids are used for the synthesis of many nitrogen-containing compounds such as | the purine and pyrimidine bases, heme , creatine , nicotinamide, serotonin, thyroxine, epinephrine , melanin, and sphingosine |
Lysosomal proteases digest | endocytosed protein |
Large cytoplasmic complexes(proteasomes)digest | older or abnormal proteins that have been covalently tagged with protein ubiquitin for destruction |
proline (P), glutamate (E), serine (S), and threonine (T) have | short half-lives. hydrolyzed by the ubiquitin-proteasome system. |
SUMO stands for | small ubiquitin-like modifier, and when proteins are tagged with it their activities are altered (either positively or negatively depending on the protein |
Pepsin is in the stomach and converts | complex proteins to small peptides |
Trypsin is in the pancreas and acts on basic amino acids | lysine, arginine, histine |
Chymtripsin | is in the pancreas and acts on aromatic amino acids phenylalanine, tyrosine, and tryptophan |
Elastase and Carboxiypeptidase acts on | Caboxy terminal amino acids |
Secretory trypsin inhibitor can cause | pancreatitis |
Neutral amino acids | (Ala, Val, Leu, Met, Phe, Tyr, Ile)0r Zwitter ions |
Basic amino acids | (Lys, Arg) and Cysteine |
Acidic amino acids | (Asp, Glu) |
Sodium–amino acid carrier system is | secondary active transport |
The L-system of amino acid transport is not dependent on sodium for cotransport. The L- system transports | branched-chain and aromatic amino acids, and will be exploited in a treatment for phenylketonuria (PKU). |
Disease related to defective membrane-transport systems of Amino acid absorption | Cystinuria, Hartnup disease |
transporter is responsible for active transport of cystine, ornithine, arginine and lysine (COAL) is defective and all four appear in urine. hexagonal kidney stones | Cystinuria |
Deficiency of tryptophan (neutral aa) transporter in proximal renal tubular cells and on enterocytes leads to clinical features of pellagra (niacin deficiency). Diarrhea, Dermatitis and Dementia | Hartnup Disease |