Some nonessential amino acids are synthesized in the body by a simple transamination. The transamination betweenoxaloacetate, an a-keto acid, and glutamate, an amino acid with the side chain -CH2CH2COO¯, proceeds according tothe following reaction:||→ -00C-CH2 CH2 C-CO0 + amino acid 20OC-CH2 CCOO +0OC-CH2 CH2 CH-COO →NH3+Predict the structure of the amino acid product, indicated by amino acid 2, for the reaction.Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Templatetoolbars. The single bond is active by default. Include all hydrogen atoms and formal charges.Viou

Some nonessential amino acids are synthesized in the body by a simple transamination. The transamination between oxaloacetate, an a-keto acid, and glutamate, an amino acid with the side chain -CH2CH2COO , proceeds according to the following reaction: OOC-CH2 C-C0O +00C-CH2CH2CH COO- 0OC-CH2CH2 C-COO +amino acid 2 NH3 Predict the structure of the amino acid product, indicated by amino acid 2, for the reaction. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Include all hydrogen atoms and formal charges.

Some nonessential amino acids are synthesized in the body by a simple transamination. The transamination between oxaloacetate, an a-keto acid, and glutamate, an amino acid with the side chain -CH2CH2COO , proceeds according to the following reaction: OOC-CH2 C-C0O +00C-CH2CH2CH COO- 0OC-CH2CH2 C-COO +amino acid 2 NH3 Predict the structure of the amino acid product, indicated by amino acid 2, for the reaction. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Include all hydrogen atoms and formal charges.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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The Fate of Carbon Atoms in Amino Acids A transamination can be summarized as an amino group (-NH3+) of an amino acid and the keto group (CO) of an a-keto acid changing places and forming different amino acid and a-keto acid products, as in the generic reaction below: amino acid 1 + a-keto acid 1a-keto acid 2 + amino acid 2 Draw the a-keto acid product of the transamination of an a-keto acid with an amino acid that has the side chain X (double click an existing atom and type X). MN [1] 7 L H: 2D EXP. CONT. ? L 7 O || R-CCOO + X Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show formal charges on all atoms. Double click an existing atom and type X to enter the side chain. ► View Available Hint(s) Marvin JS by ChemAxon H C N O S CI Br I P +H3N-CH-C-0- F < 18 of 20 →?
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What is the name of the point at which the amino acid shown here exists? O H₂N-CH-C-O CH₂ A) acidic point B) basic point C) neutral point D) isoelectric point E) ionized point
Which of the following statements is false concerning the structure of hemoglobin? O The R-state of Hb is favored under environments of high concentrations of O2 The binding of BPG stabilizes the low affinity state of Hb O Hemoglobin is stabilized in the low affinity state in the presence of high concentration of protons Hemoglobin's affinity for oxygen increases in the presence of carbamates O Hemoglobin favors the R-state in basic environments
ollowing reactions are part of the citricam The numbers in parenthesis indicate the ror carbon atoms in each molecule. Isocitrate( 6 ) →��-ketoglutarate(5) →Delta succinyl CoA(4) longrightarrow succinate (4)→� fumarate(4) Which of the following sequences of the rot systems �→� is correct? 3 3 (1) ��2→��++�+→��+,��2→NADH+ ��2→ GTP, FAD , IP →�� (��2) (2) ��+→NADH+�+,��+,��2→NADH+�+ ��2→ATP,FAD,��→��2 (3) ��+→NADH+�+,��+,��2→��2,��++ ��**, iP →��+�+,��2 (4) ��+→��++�+,��+,��+→+�� →��2��+, iP →NADH+�+,��2