Molecular tools that perform an astonishing variety of functions in addition to serving as structural materials in all living organisms
Proteins
Involved in catalysis, metabolic regulation, transport, and defense
Composed of one or more polypeptides, unbranched polymers of 20 different amino acids
The genomes of most organisms specify the amino acid sequences of thousands or tens of thousands of proteins
This unit begins with an introductory discussion on the structures and chemical properties of amino acids, the building blocks of proteins
This is followed by descriptions of the structural and functional features of peptides and proteins and the protein folding process
The emphasis of presentation is on the intimate relationship between the structure and function of polypeptides
This unit deals with the classification, physical and chemical properties, color reactions that help in the identification of an amino acid which is the repeating unit of proteins
It also discusses separation methods and determination of amino acid sequence, the four levels of protein structure, and interactions that stabilize these structures as well as the denaturation process of proteins
Amino acids
The building blocks of proteins
Amino acids
They are -amino acids, so named because the amino group is bonded to the carbon atom, next to the carbonyl group
The physical and chemical properties of a protein are determined by its constituent amino acids
The individual amino acid subunits are joined by amide linkages called peptide bonds
Isoelectric pH (pI)
The pH at which the net charge an amino acid is zero
Amino acids with acidic side chain contain an extra carboxylic group, because of this they tend to become polar and ionizable
Proline
The only cyclic amino acid, also known as imino acid
Polar neutral amino acid
An amino acid with a polar but uncharged side chain
Ketogenic amino acids
Amino acids that break down to form ketone bodies
Non-essential amino acid
An amino acid that can be synthesized by the body and does not need to be obtained from the diet
Standard amino acid
An amino acid composed of C, H, O, N, and sometimes S
Disulfide bond
A covalent bond formed between the sulfur atoms of two cysteine residues
Amino acids as fuel source
The carbon skeletons of amino acids are used in the citric acid cycle to produce energy
Tyrosine
Amino acid that contains a phenol group
Arginine
Amino acid containing guanidine group
pK2
The ionization value assigned to the carboxyl group of an amino acid
Ninhydrin
Reagent used to detect the presence of arginine in a qualitative test
Ninhydrin
A chemical used to detect ammonia or primary and secondary amines which can also be used to visualize fingerprints
Tryptophan
The amino acid that contains a 2-ring system known as indole group
Isoelectric point (pI)
The pH at which the net charge an amino acid is zero
Biuret test
A test used for the detection of aromatic amino acids tyrosine, tryptophan, and phenylalanine in a protein solution
The magic words are: PROLINE, TYROSINE, ARGININE, CARBOXYL, NINHYDRIN, TRYPTOPHAN, ISOELECTRIC POINT, BIURET
Protein
A biomolecule or macromolecule that contains the building blocks called amino acids whose primary structure is a linear sequence of -amino acids and whose final structure results from folding of the chain into a specific three-dimensional structure
Proteins are the most versatile macromolecules in living systems and serve crucial functions in essentially all biological processes
Proteins
They function as catalysts, they transport and store other molecules such as oxygen, they provide mechanical support and immune protection, they generate movement, they transmit nerve impulses, and they control growth and differentiation
Protein function depends on the linear sequence of amino acids
Proteins spontaneously fold up into three-dimensional structures that are determined by the sequence of amino acids in the protein polymer
Proteins
They contain a wide range of functional groups including alcohols, thiols, thioethers, carboxylic acids, carboxamides, and a variety of basic groups
They can interact with one another and with other biological macromolecules to form complex assemblies
Some are quite rigid, whereas others display limited flexibility
Amino acids
Organic compounds that contain amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid
About 500 naturally occurring amino acids are known (though only 20 appear in the genetic code)
amino acids
Amino acids where the stereogenic carbon alpha to the amino group has the D-configuration
Only L-amino acids are manufactured in cells and incorporated into proteins
All naturally occurring proteins from all living organisms consist of L-amino acids
Classification of amino acids based on nutrition and metabolic fate
Essential amino acids
Non-essential amino acids
All amino acids except glycine are chiral because they all contain at least one chiral center