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107 Cards in this Set

  • Front
  • Back
needed to hydroxylate proline for collagen synthesis
Ascorbate (Vit C)
needed to move around methyl groups and other rearrangements
B12
precursor to two molecules of vitamin A
beta-carotene
needed for carboxylation reactions
Biotin
needed for the transfer of single carbons (methyl, formal…)
Folate B9
needed for two major dehydrogenase enzymes
Lipoate
needed for synthesis of NAD+
Niacin (B3)
needed to make CoA and other similar molecules like ACP
Pantothenic acid B5
needed for transamination
Pyridoxal phosphate (B6)
needed for synthesis of FAD
Riboflavin (B2)
needed for aldehyde associated reactions
Thiamine (B1)
need to make retinol and other molecules
Vitamin A
fat soluble vitamin needed for calcium uptake
Vitamin D
fat soluble vitamin that functions as an antioxidant
Vitamin E
fat soluble vitamin needed for blood clotting
Vitamin K
site III inhibitor of the ETC
antimycin A
interferes with the use of phosphate glycolysis G13BP
Arsenate poisoning
binds to sulfurs on lipoate
Arsenite poisoning
prevents ATP from leaving mitochondria by blocking ADP/ATP antiporter
atractyloside
blocks the release of acetyl choline at the neuromuscular junction
Botulinum toxin
binds Fe+2 of hemoglobin, myoglobin and Site for of ETC
Carbon Monoxide
adenylates the G-alpha-s protein so it can't hydrolyse GTP inc cAMP
Cholera toxin
arrow poison
Curare
site IV inhibitor of the ETC on Fe+3
cyanide
uncoupling agent Site 4
dinitrophenol
suicide inhibitor of glyceraldehyde dehydrogenase
Iodoacetate poisoning
blocks the acetylcholinesterase, allowing acetylcholine levels to remain high
Nerve Gas
activates the N type of acetyl choline receptors
Nicotine
ATP synthase inhibitor in the mitochondria
oligomycin
arrow poison
Ouabain
adenylates the G-alpha-i protein so it can't bind GTP
Pertussis toxin
agonist for PKC cancer
phorbol ester
site I inhibitor of the ETC
rotenone
red tide na K
Saxitoxin
puffer fish Na K
Tetrodotoxin
substitutes for phosphate
Vanadate
needed for entry of FFA into mitochondria
carnitine
the electron carrier in the ETC between sites I and II, going to site III
Co-Q
indigestible carbohydrate
dietary fiber
glucose aminoglucose
Glucosamine
marker for past insulin levels
C-peptide
marker for past glucose levels
HbA1c
uptake of glucose, synthesis of glycogen, fat and protein
insulin
suicide inhibitor of cyclooxygenase (COX)
Aspirin
blocks epi/norepi receptors
Beta-blocker
one mechanism is to block cAMP phosphodiesterase
Caffeine
competitive inhibitor of cyclooxygenase (COX)
Ibuprofen
treatment of diabetes
Insulin therapy
used for lactose intolerance
lactase supplements
decomposes to nitric oxide
Nitroglycerine therapy
non-steroidal anti-inflammatory drug - inhibit COC
NSAID
pancreatic lipase inhibitor
Orlistat
cGMP phosphodiesterase inhibitor
Sildenafil
HMG-CoA reductase inhibitor
statins
outward potassium channel blockers in the pancreas
Sulfonylureas
deficiency of liver aldolase - need for fructose and glucose metabolism
Aldolase B deficiency
Branching enzyme defect
Anderson Disease AB vs CD
microorganism that produces cholera toxin
Cholera
Debranching enzyme
Cori Disease CD
rare spontaneous refolding of the prion protein
Creutzfeldt-Jakob disease
defective chloride ion channel
cystic fibrosis
fructokinase deficiency
Essential fructosuria
defect in the LDL receptors
Familial Hypercholesterolemia
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PDD)
Favism
defect of fructose uptake in intestine
Fructose Intolerance
galactokinase or glucose/galactose epimerase
Galactosemia
lysosomal storage disorder, defective glucocerebrosidase
Gaucher's disease
defect of PPP, failure to produce NADPH, failure to protect from free radicals
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PDD)
build of uric acid
Gout
desctruction of red blood cell membranes
hemolytic anemia
Liver Phosphorylase
Hers Disease
defect in the synthesis of mannose-6-phosphate on glycoproteins
I-cell disease
defective in recycling purine nucleotides, decrease in pyrimidines
Immunodeficiency
insulin producing pancreas tumor
Insulinoma
refolding of the prion protein due to injection of misfolded human prion
Kuru
lack of expression or defect in the enzyme lactase
Lactose Intolerance
autoimmune attack on the Ca channels on motor neurons of the neuromuscular junction
Lambert–Eaton myasthenic syndrome
defective in recycling purine nucleotides, build of uric acid in brain
Lesch-Nyhan syndrome
refolding of the prion protein due to ingestion of misfolded cow prion
Mad Cow Disease
inability to catabolize fatty acids of medium length
MCAD
Muscle Phosphorylase
McArdle Disease
pancreatic glucokinase deficiency
MODY
autoimmune attack on the N1 receptors in the neuromuscular junction
Myasthenia gravis
pellagra B3 pelle = skin; agra = sour headaches, confusion, and loss of appetite.
Niacin deficiency
lysosomal storage disorder
Niemann-Pick disease
can't digest starch
Pancreatic Amylase Deficiency
microorganism that produces Pertussis toxin
Pertussis
Lysosomal glucosidase
Pompe Disease
Vitamin D deficiency
Rickets
refolding of the prion protein due to ingestion of misfolded sheep prion
Scrapie
a val substituted for a glu at beta 6 of hemoglobin
sickle cell anemia
can't digest table sugar
Sucrose-Isomaltase deficiency
lysosomal storage disorder, defective hexamidase A
Tay-Sachs disease
inability to decarboxylate or rearrange, blocks non-oxidative PPP
Thiamine Deficiency B1
can't digest sugar found in mushroom, honey and shrimp
Trehalase deficiency
muscle PFK-1
Type 7 GSD
liver phosphorylase kinase
Type 8 Glycogen Storage Disorder (GSD)
pancreas fails to produce insulin
Type I diabetes
Glucose-6-phosphatase
Von Gierke Disease
high blood glucose
Hyperglycemia
build up of bilirubin in skin due to liver failure
jaundice
decrease in blood pH due to increased concentration of ketone bodies
ketoacedosis
iron of hemoglobin in Fe+3 state
Methemoglobinemia
indication of diabetes
reducing sugar in urine
Fake Fat
Olestra
bis phosphoglycerate
BPG
Sickle cell hemoglobin
HbS