Amino Acids Flashcards
Essential Amino Acids
Histidine Methionine Threonine Valine Isoleucine Phenylalanine Tryptophan Leucine Lysine
PVT TIM HALL
What is the metabolic fate of AA’s?
Intermediary metabolism
What is intermediary metabolism?
- Synthesis of needed compounds
- Storage of energy rich compounds: fats and carbohydrates
- Breakdown of compounds
What two compounds are broken down?
Carbon: Extraction of energy
Carbon flows into TCA
Nitrogen: Excrete in water soluble form: urea in urine
Nitrogen flows into the urea cycle
AA’s with Polar Uncharged Side Chains
Chemically reactive side chains
Cysteine, serine, threonine, tyrosine
Cysteine
sulfhydryl group (-SH) Active site of many enzymes Disulfide bond formation to stabilize protein structure
Serine, Threonine, Tyrosine
Transient phosphorylation in signaling proteins
Serine and Threonine
Oligosaccharide attachment points
Primary Protein Structure
linear sequence of AA’s specified by DNA/RNA
Secondary Protein Structure
local neighborhoods on linear sequence resulting from interactions of adjacent AA functional groups
Tertiary Protein Structure
long distance interactions between AA neighborhoods
Quaternary Protein Structure
interaction between individual protein chains
Polymorphisms
Variations in codons
Result in same or similar code
Functional consequences small (but not necessarily trivial)
Functional consequences
Variation in susceptibility to disease
Variation in drug metabolism
Variation in host response to stress, injury, infection, and disease
Basis of personalized medicine
Major functional consequences
major change in class of AA Mutation Genetic disease - loss of function - gain of function (gain of toxicity)