Biochemistry AA Metabolism u 2 b o i x q i u d 5 a i a l t t 8 k i i k a a n v e 10 p a o e t t t r d o 12 g o i n e g 14 l a n i n e t y r o s i n a s e u u r n t m n t r y h i i a i p i n c m a s n a i i e t n o s u c c i n a t e i e o n 1 t r i 7 a p m m o n e m i i p n t o i 13 p d a s e e p s t i n u r i i 18 d n 19 a r g i n i s t e r o g e t o n i n b a l a 24 t r a n s a m i n a s e c e 3 c i t r u l l i 15 a m i n o 16t r a e r a n s a 20 h i s t a m i n i 21 p n y a r t i i d o 23 z y m o g e n x a l p h o s p h a t e 4 p h 9 h y p e r a n 11 y u l r k e n s f e r a t c 17 h o m o c y n c u l r e e i a 6 s e r o 22 Across Down ✓9. A metabolic condition characterized by elevated levels of ammonia in the blood ✓1. A post-translational modification that marks proteins for degradation. ✓13. Plays a special role in transporting amino groups from the muscle to the liver in a nontoxic form. ✓2. Removal of amino groups are removed from amino acids, resulting in the formation of corresponding keto acids and ammonia. (2 words) : ✓14. A mutation of this enzyme (due to genetic defect) resulting in reduced melanin production that leads to albinism. ✓15. An enzyme that catalyzes transamination reaction between an amino acid and an alpha-keto acid. ✓17. A rare metabolic condition characterized by an excess of the compound homocystine in the urine. ✓19. A precursor to fumarate and arginine in the urea cycle via argininosuccinate lyase. ✓20. An organic nitrogenous compound produced as part of a local immune response to cause inflammation. It could be derived from histidine decarboxylation. ✓22. A neurotransmitter produced via the hydroxylation and decarboxylation of tryptophan. ✓23. An inactive precursor of an enzyme. ✓24. Another name for the enzyme that catalyzes transamination reaction between an amino acid and an alpha-keto acid. ✓3. A peptide derived from three amino acids joined by two or sometimes three peptide bonds. ✓4. The compound is formed by transferring carbamoyl portion of carbamoyl phosphate to ornithine by ornithine transcarbamylase (OTC). The compound formed is released into the cytosol for use in the rest of the steps of the urea cycle. ✓5. An inherited condition that causes urine to turn black when exposed to air, due to the fact that the body could not breakdown the amino acids phenylalanine and tyrosine. ✓6. An inborn error of metabolism caused by a deficiency of phenylalanine hydroxylase. ✓7. An enzyme that catalyzes the cleavage of amino acids from the amino terminus of protein or peptide substrates. ✓8. Describes an amino acid that can be degraded directly into acetylCoA, and ultimately acetoacetyl-CoA. ✓10. One of the intermediate metabolites of the urea cycle that is generated in the cytosol from arginine and transported into the mitochondria for following reactions. ✓11. A cycle of biochemical reactions in which nitrogen from protein metabolism is converted to urea. (2 words) ✓12. The main form of nitrogen transporter between tissues. ✓14. An endopeptidase secreted by the pancreas to aid in the digestion of foods. Functions to activate other pancreatic zymogens as well. ✓16. A reversible reaction that transfers an amino group to a ketoacid to form new amino acids. ✓18. Refers to the difference between the amount of nitrogen taken in and the amount excreted or lost. Mainly used to evaluate nutritional balance. (2 words) : ✓21. An essential metabolism cofactor derived from Vitamin B6. (2 words)