| Term 
 | Definition 
 
        | these 2 amino acids are exclusively ketogenic |  | 
        |  | 
        
        | Term 
 
        | Isoleucine, Phenyalanine, Tyrptophan, Tyrosine, Threonine |  | Definition 
 
        | Name the ketogenic and glucogenic AA's |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | aspargine is deaminated by ____ yeilding asparate and ammonia and this can be used to treat Leukemia |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Glutamine is deaminated by this enzyme to form glutamate |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Glutamate-->alpha ketoglutarate is a transaminase reaction catalyzed by what enzyme? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | What does the histidine load test measure to estimate folate cells? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | If we have a block of histidase what product will not be produced? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | alanine, cystine, glycine, serine, threonine can all be converted to ? |  | 
        |  | 
        
        | Term 
 
        | phenyalanine hydroxylase; THB |  | Definition 
 
        | when phenyalanine is converted to tyrosine, what is the enzyme and its cofactor? |  | 
        |  | 
        
        | Term 
 
        | fumarate and acetoacetate |  | Definition 
 
        | what are the two products that tyrosine can form? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | this disease is caused by a deficiency in tyrosine metabolism and phenyalanine hydroxylase |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | What does phenyalanine hydroxylase require as a coenzyme? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | The intermediate stage from Isoleucine and Valine--> succinyl CoA is? what vitamin does it involve? |  | 
        |  | 
        
        | Term 
 
        | Propionyl CoA carboxylase |  | Definition 
 
        | If you have a biotin deficiency and you see a build up of propionyl CoA, what enzyme is deficient? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Mehtylmalonic Aciduria is unresponsive to B12 and it is associated with developmental retardation and chronic metabolic acidosis. What is the deficient enzyme? |  | 
        |  | 
        
        | Term 
 
        | Isoleucine, Leucine, Valine, and Tryptophan |  | Definition 
 
        | what are the four essential AA's |  | 
        |  | 
        
        | Term 
 
        | Branched chain alpha keto acid dehydrogenase |  | Definition 
 
        | MSUD is caused by what type of deficiency? |  | 
        |  | 
        
        | Term 
 
        | Methalonyl CoA+ Succinyl CoA |  | Definition 
 
        | In the biosynthesis of Nonessential Amino acids the two end products formed by Valine are? |  | 
        |  | 
        
        | Term 
 
        | Acetyl CoA and Propionyl CoA |  | Definition 
 
        | In the biosynthesis of Nonessential Amino acids the two end products formed by Isoleucine? |  | 
        |  | 
        
        | Term 
 
        | acetyl CoA and acetoacetate |  | Definition 
 
        | In the biosynthesis of Nonessential Amino acids the two end products formed by Leucine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | tyrosine hydroxylase and tryptophan hydroxylase requires this co-enzyme |  | 
        |  | 
        
        | Term 
 
        | Guthrie Card Bacteria Assay |  | Definition 
 
        | What is the test that is used to asses Maternal PKU? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | this is driven by hydrolysis of all 3 phosphate bonds in ATP |  | 
        |  | 
        
        | Term 
 
        | Cystathinonine Beta Synthase |  | Definition 
 
        | What is the enzyme that is deficient in Homosytinuria? |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Complete albinism results from a deficiency of _____ activity |  | 
        |  | 
        
        | Term 
 
        | homogenetisic acid oxidasse |  | Definition 
 
        | Alkaptonuria is caused by a deficiency in this enzyme resulting in accumulation of homogentisic acid |  | 
        |  |