Step 1 Krebs Cycle. 77. Inhibited by a high concentration of ATP that joins at allosteric site. 78. PEP loses phosphate group through substrate level phosphorylation. 79. Isomerization changes the configuration of atoms in the compound. 80. Acts to combine acetyl-group to oxaloacetate. 81. Produced by the oxidation of a-Ketoglutarate.
Step 1 Krebs Cycle. 77. Inhibited by a high concentration of ATP that joins at allosteric site. 78. PEP loses phosphate group through substrate level phosphorylation. 79. Isomerization changes the configuration of atoms in the compound. 80. Acts to combine acetyl-group to oxaloacetate. 81. Produced by the oxidation of a-Ketoglutarate.
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Question
76. Step 1 Krebs Cycle.
77. Inhibited by a high concentration of ATP that joins at allosteric site.
78. PEP loses phosphate group through substrate level phosphorylation.
79. Isomerization changes the configuration of atoms in the compound.
80. Acts to combine acetyl-group to oxaloacetate.
81. Produced by the oxidation of a-Ketoglutarate.
82. Final destination of electrons after
83. Provides Pi for substrate level phosphorylation of ATP in Krebs cycle.
84. Pyruvate oxidation by NAD+ forms a waste product.
85. Activates glucose to start cellular respiration.
choices:
a. isocitrate
b. succinate
c. NAD+
d. malate
e. succinyl-CoA
f. Oxaloacetate
g. Sulfur
h. a-ketoglutarate
i. fumarate
j. ATP
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