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