Draw the oligopeptides' structure and provide the corresponding name for each oligopeptide 1. Dipeptide Ala-His 2. Tripeptide Glu-Pro-Cys Note: First residue is the N-terminal amino acid

Write the name for the trisaccharide depicted below (for example, of the form a - D - xylofuranose). Be sure to include if the sugars are in the pyranose or furanose conformations in the name and include the linkages between sugars (for example, (2 - - > 4)). CH₂OH ОН OH н ОН -CH₂ H\H ОН н н ОН CH2OH н ОН но н н ОН

Identify the following types of biomolecules and label and identify the functional groups

Identify the structure of the predominant form of the pentapeptide at pH = 12 if there is a pentapeptide Ile-Lys-Asp-Phe-Gly

Create an oligopeptide via dehydration synthesis using the following amino acids. O. H Tryptophan (TRP) C-C-N но сн, C-C-N. но Glycine (GLY) H H HN

Ala Leu Glu Glu Asn Ala represent the following amino acid in its predominant form at pH= 7

What would be the structural formula of the oligopeptide if the amino acids are arginine, glutamine, glycine, methionine and glutamic acid considering the first amino acid is the N-terminus

The human body uses the branched polymer glycogen for short term storage of glucose in the liver. It is broken down by the stepwise removal of the terminal glucose monomer. Explain why it is an advantage for glycogen to have a branch chain structure rather than a linear structure.   (A pargraph would be great)

Which of the following amino acids would you least expect to find on the surface of a water-soluble protein? Explain I Serine Glutamat Lysime Threonine