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This set of flashcards covers key terms and concepts related to proteins, amino acids, and their metabolic processes as discussed in Chapter 6.
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Proteins
Large, complex molecules found in cells of all living things, dictated by genetic material (DNA) and made from 20 different amino acids.
Amino Acids
Building blocks of proteins, with a structure that includes a central carbon, an amine group, a carboxyl group, and a variable side chain.
Essential Amino Acids
Amino acids that cannot be produced in sufficient quantities by the body and must be obtained through food.
Nonessential Amino Acids
Amino acids that can be synthesized by the body in sufficient quantities.
Transamination
The process by which an amine group is transferred from one amino acid to another.
Peptide Bond
The bond formed between two amino acids through a condensation reaction, releasing water.
Protein Turnover
The process of degrading existing proteins to provide the building blocks for new proteins.
RNA
Ribonucleic acid that carries genetic information from DNA to the ribosome for protein synthesis.
Transcription
The process of copying the DNA sequence into messenger RNA (mRNA) in the nucleus.
Translation
The process of translating the sequence of mRNA into a sequence of amino acids at the ribosome.
Urea Excretion
The process by which excess nitrogen from protein metabolism is converted to urea in the liver and excreted in urine.
Protein Digestion
The process of breaking down dietary proteins into single amino acids primarily in the stomach and small intestine.
Nitrogen Balance
The state achieved when nitrogen intake equals nitrogen excretion in the body.
Complete Proteins
Proteins that contain all essential amino acids in adequate amounts.
Incomplete Proteins
Proteins that are lacking one or more essential amino acids.
Mutual Supplementation
Combining different food sources to make a complete protein.
High Protein Diets
Diets that may pose risks for heart disease, bone health, and kidney disease but can also provide benefits.
Sickle Cell Anemia
A genetic disorder resulting from a mutation that affects hemoglobin production, causing red blood cells to become rigid and sickle-shaped.