The cell nucleus and mitochondria are some examples.
What are some non examples of weathering are everything that has to do with no rocks
non-examples of nucleic acid
the answer is C (144). The working is: 12^2 = 144. Here 12 is the no. of different amino acids and 2 is the no. of amino acids in the chain (its a dipeptide so, 2 amino acids).
H
Yep, dipeptides cyclize and polymerize at room temperature
Polypeptides and dipeptides
Dipeptides are defined as two amino acids joined by a peptide bond or a single amino acid with two peptide bonds. Different dipeptides have different functions. Kyotorphin, for example, helps with pain regulation in the brain while carnosine inhibits diabetic nephropathy.
A few dipeptides in the human body may include carnosine (brain), kyotorphin (also in brain), opidine (muscles), and anserine (skeletal).
Dipeptides.
dipeptides
Two.
Hydrolysis reactions break apart dipeptides to make two amino acids. Condensation (dehydration) reactions take two amino acids and make one dipeptide.
Dipeptides and polypeptides are made from amino acids joined together by peptide bonds. Dipeptides consist of 2 amino acids, therefore are joined by a single peptide bond. Polypeptides are made from lots of amino acids. Amino acids are the monomer, there are about 20 naturally occurring amino acids. When they are becoming linked in a peptide bond, they combine in a condensation reaction releasing water.
Enzymes such as Trypsin, Chymotrypsin and Carboxy peptidase converts the Proteins, Peptons & proteoses into Dipeptides... Then Dipeptidase convert the dipeptides into Amino acids.. Finally this amino acids are absorbed by villi of small intestine... This happens to the Protein molecules we eat..
When dietary proteins are digested they turn into dipeptides and amino acids. The dipeptides are then absorbed more rapidly than the amino acids and they activate the G-cells in the stomach to secrete gastrin. Which in turn controls the production of the stomach acids.
An azadipeptide is any of a group of aromatic dipeptides which have an N-N group in place of the terminal amine.