Exam 2 (Lectures 14-16) Flashcards

(115 cards)

1
Q

Vitamins

A

organic small molecules needed to trace amounts from the diet

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2
Q

Many vitamin derivatives are…

A

coenzymes

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3
Q

Carrier Molecule: ATP

A

Phosphoryl carrier

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4
Q

Carrier Molecule: NADH and NADPH

A

Electron Carrier

Vitamin precursor: Nicotinate (niacin)

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5
Q

Carrier Molecule: FADH2 and FMNH2

A

Eclectron carrier

Vitamin Precursor: Riboflavin (Vit B2)

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6
Q

Carrier Molecule: Coenzyme A

A

Acyl carrier

Vitamin precursor: Pantothenate

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7
Q

Carrier Molecule: Lipoamide

A

Acyl carrier

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8
Q

Carrier Molecule: Thiamine pyrophosphate

A

Aldehyde carrier

Vitamin precursor: thiamine (Vit B1)

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9
Q

Carrier Molecule: Biotin

A

CO2 carrier

Vitamin precursor: biotin

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10
Q

Carrier Molecule: Tetrahydrofolate

A

One-carbon unit carrier

Vitamin precursor: folate

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11
Q

Carrier Molecule: S-Adenosylmethionine

A

Methyl carrier

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12
Q

Carrier Molecule: Uridine diphosphate glucose

A

Glucose carrier

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13
Q

Carrier Molecule: Cytidine diphosphate diacylglycerol

A

Phosphatidate carrier

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14
Q

Carrier Molecule: Nucleoside trphosphates

A

Nucleotide carrier

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15
Q

Thiamine (B1)

A

Coenzyme: thiamine pyrophosphate

Rxn Type: aldehyde transfer

Deficiency: beriberi (weight loss, heart probs, neurological dysfunction)

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16
Q

Riboflavin (B2)

A

Coenzyme: flavin adenine dinucleotide (FAD)

Rxn Type: RedOx

Deficiency: cheliosis and angular stomatitis (lesions of the mouth), dermatitis

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17
Q

Pyridoxine (B6)

A

Coenzyme: Pyridoxal phosphate

Rxn Type: group transfer to or from amino acids

Deficiency: depression, confusion, convulsions

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18
Q

Nicotinic Acid (B3)

A

Coenzyme: nicotinamide adenine dinucleotide (NAD+)

Rxn Type: RedOx

Deficiency: pellagra (dermatitis, depression, diarrhea)

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19
Q

Pantothenic Acid (B5)

A

Coenzyme A

Rxn Type: acyl-group transfer

Deficiency: hypertension

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20
Q

Biotin (B7)

A

Coenzyme: biotin-lysine adducts (biocytin)

Rxn Type: ATP-dependent carboxylation and carboxyl-group transfer

Deficiency: rash about the eyebrows, muscle pain, fatigue

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21
Q

Folic Acid (B9)

A

Coenzyme: tetrahydrofolate

Rxn Type: transfer of one-carbon components; thymine synthesis

Deficiency: anemia, neural-tube defects in development

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22
Q

B12

A

Coenzyme: 5’-deoxyadenosyl cobalamin

Rxn Type: transfer of methyl groups; intramolecular rearrangements

Deficiency: anemia, pernicious anemia, methylmalonic acidosis

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23
Q

Lipid Soluble Vitamines:

A

Vit K1, Vit A, Vit E, Vit D2

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24
Q

Noncoenzyme Vitamins

A

A, C, D, E, K

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25
Vitamin A
roles in vision, growth, reproduction
26
Vitamin C
water soluble vitamin as an antioxidant Deficiency: Scurvy (swollen and bleeding gums)
27
Vitamin D
regulation of calcium and phosphate metabolism Deficiency: Rickets (children): skeletal deformaties, impaired growth Osteomalacia (adults): soft bending bones
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Vitamin E
Antioxidant Deficiency: inhibition of sperm production, lesions in muscles and nerves
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Vitamin K
Blood coagulation Deficiency: subdermal hemorrhaging
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What are the types of chemical reactions in metabolism?
RedOx, Ligation requiring ATP cleavage, Isomerization, Group transfer, Hydrolytic, Addition or removal of funtional groups
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Ligation requiring ATP cleavage
formation of covalent bonds
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Isomerization
rearrangement of atoms to form isomers
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Group Transfer
transfer of a functional group from one molecule to another
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Hydrolytic
cleavage of bonds by the addition of water
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Addition or removal of functional groups
addition of functional groups to double bonds or their removalto form double bonds
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Things that are charged and/or bulky...
cannot move well across membranes
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The overall free energy change for a couple set of reactions... A ⇔ B + C B⇔ D
is the sum of the change in free energy for individual reactions
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Creatine phosphate
an important molecule for storage of high energy phosphate groups
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What can drive the unfavorable reaction forward?
coupling of energetically unfavorable reactions to favored reactions
40
Oxidation of foods, carbohydrates, and fats yield...
CO2, energy, and reducing equivalents
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Reducing Equivalents
electrons with high transfer potential used to create an ion gradient across a membrane the electrochemical potential produced by this dude is used to power the synthesis of ATP
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Harvesting ATP from food
Stage 1: food is broken down into smaller compounds Stage 2: Glycolysis Stage 3: Citric Acid Cycle or TCA or Kreb's
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Harvesting ATP from food: Stage 1
Breakdown of food into smaller compounds such as: proteins to amino acids complex carbohydrates to simple sugars fats to glycerol and fatty acids
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Harvesting ATP from food: Stage 2
Glycolysis: when glucose and other simple sugars are broken down to generate CoA Some ATP is generated in this stage
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Harvesting ATP from food: Stage 3
Critric Acid Cycle or TCA or Kreb's acetyl CoA group is fully oxidized to CO2 and electrons are produced Most of ATP is generated in this stage Occurs in the mitochondrion
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Activated Carriers that are required in ATP Harvest
carriersof high energy electrons for fuel oxidation NAD+ and FAD
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Carbohydrates
organic molecules with the fomula: (CH2O)n
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Immediate Energy sources:
Glucose and Fructose
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Stored sugar:
Glycogen and Starch in plants
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Carbohydrates function as...
Energy source Provides structure Participate in Cell interactions
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Carbohydrates: Energy Source
Immediate energy source Stored Sugars Metabolic intermediates
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Carbohtdrates: Provide Structure
Cellulose (glucose polymer) Chitin (sugar derivative) Ribose and bacterial cell wall are roughly made from sugar
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Carbohydrates: participate in cell interactions
Glycoproteins Proteoglycans Glycolipids
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Glycoproteins
cell surface molecules involved in cell to cell interaction Cell ID ABO groups
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Proteoglycans
molecules of the ECM Chondroitin sulfate Heparan sulfate
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Isomers
compounds with the same chemical formula
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Stereoisomers
isomers with different configurations
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Enantiomers
stereoisomers that are mirror images of one another
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Diastereomers
stereoisomers that are not mirror images of one another
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Epimers
diastereomers differing at only one asymmetric carbon
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D and L in the names
designate the absolute configuration of the asymmetric carbon furthest from the aldehyde or ketone group D sugars are commonly seen
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D-Glyceraldehyde
[![](http://upload.wikimedia.org/wikipedia/commons/f/fe/D-Glycerinaldehyd.png)](http://www.google.com/url?sa=i&rct=j&q=&esrc=s&source=images&cd=&docid=e3O-wMg83iTSqM&tbnid=N_nhCRBjM_L0YM:&ved=0CAcQjRw&url=http%3A%2F%2Fen.wikibooks.org%2Fwiki%2FStructural_Biochemistry%2FOrganic_Chemistry%2FStereochemistry&ei=4dAyVNfpAYqRyASFt4GACA&bvm=bv.76802529,d.aWw&psig=AFQjCNF3EjEBoOV14GPO04A-EgZVRndogw&ust=1412702813167084)
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D-Ribose
[![](http://www.uspto.gov/web/patents/classification/uspc536/c536s1-11-1.gif)](http://www.google.com/url?sa=i&rct=j&q=&esrc=s&source=images&cd=&docid=v2IHf2aSIpz9EM&tbnid=EkAWkwGRt4WzxM:&ved=0CAcQjRw&url=http%3A%2F%2Fwww.uspto.gov%2Fweb%2Fpatents%2Fclassification%2Fuspc536%2Fdefs536.htm&ei=OtEyVNmzHoWnyQSKxoAg&bvm=bv.76802529,d.aWw&psig=AFQjCNGq42QWWyW51TG6VkQ6ZvLK-oN0pw&ust=1412702899097976)
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D-Glucose
[![](http://science.uvu.edu/ochem/wp-content/images/H/haworthformula3.png)](http://www.google.com/url?sa=i&rct=j&q=&esrc=s&source=images&cd=&docid=OEaJSA1PEdismM&tbnid=1HSYTuxw5y1GZM:&ved=0CAcQjRw&url=http%3A%2F%2Fscience.uvu.edu%2Fochem%2Findex.php%2Falphabetical%2Fg-h%2Fhaworth-formula%2F&ei=KtIyVJzfLYinyATj0YK4Cg&bvm=bv.76802529,d.aWw&psig=AFQjCNFx3P7FDstQuE1uH6pU_BfyrZntpg&ust=1412703139572323)
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D-Mannose
[![](http://www.chemeddl.org/resources/models360/files/161658/d-mannose-fischer.png)](http://www.google.com/url?sa=i&rct=j&q=&esrc=s&source=images&cd=&docid=OrDtk8L06v3-KM&tbnid=q_0_vFQuACLBTM:&ved=0CAcQjRw&url=http%3A%2F%2Fwww.chemeddl.org%2Fresources%2Fmodels360%2Fmodels.php%3Fpubchem%3D161658&ei=aNIyVPvoLsKHyAS2l4KYDA&bvm=bv.76802529,d.aWw&psig=AFQjCNEReL6_C6mAeQwRuMU1VLb6C7hcHA&ust=1412703186755212) ## Footnote
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D-Galactose
[![](http://www.chemeddl.org/resources/models360/files/6036/d-galactose-fischer.png)](http://www.google.com/url?sa=i&rct=j&q=&esrc=s&source=images&cd=&docid=rDu0xRq8XLBf8M&tbnid=MnvX3QjK3rMy3M:&ved=0CAcQjRw&url=http%3A%2F%2Fwww.chemeddl.org%2Fresources%2Fmodels360%2Fmodels.php%3Fpubchem%3D6036&ei=oNIyVNLBOs2gyATTgoKAAQ&bvm=bv.76802529,d.aWw&psig=AFQjCNHSzVHw9EcsN26cHN-RcybJ6j-kPg&ust=1412703260104652)
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Dihydroxyacetone
![](http://images.flatworldknowledge.com/ballgob/ballgob-fig16_x017.jpg)
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D-Fructose
![](http://upload.wikimedia.org/wikipedia/ja/5/59/D-Fructose-Fischer.PNG)
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Glycosides
acetals of carbohydrates
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Glycosidic Bonds
bonds that result in formation of an acetal N- or O-glycosidic (Nitrogen- or Oxygen-)
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A glycosidic bond between 2 monosaccharides produces...
a disaccharide attached through an ether linkage
72
Where are the anomeric carbons for aldoses and ketoses?
in C1 and C2 respectively
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Sucrose
transport form of plant sugar; 1 α → 2 ß glucose - fructose ![](http://www.southernmatters.com/sugarcane/images/sucrose2.jpg)
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Lactose
milk sugar; 1 ß → 4 α galactose - glucose ![](http://www.galilu.com/chem/lactose.gif)
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Maltose
breakdown product of starch 1 α → 4 α glucose - glucose ![](http://themedicalbiochemistrypage.org/images/maltose.jpg)
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Which disaccharides is not a reducing sugar?
Sucrose because both of the anomeric carbons are unable to open up since C1, glucose, is an acetal and C2, fructose, is a ketal
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What are the storage forms of glucose?
cellulose, starch and glycogen
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Activated Sugar
linked in an enzyme-catalyzed reaction to a target molecule
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Carbohydrates can be attached to proteins through...
N- or O- linkage to asparagine or serine residues
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glycoproteins
glycosylated proteins
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Major component in proteoglycan is...
sugar
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N-linked sugars are added in...
endoplasmic reticulum en bloc from an ER carrier lipid, dolichol phosphate
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GlcNac N-acetylglucosamine
it is a carbohydrate derivative
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N-linked sugars are processed in...
the golgi apparatus, some sugars are removed and added until it reaches its final configuration
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Dolichol Phosphate
an activated dolichol that is a lipid found in the lumenal face of the ER platform that polysaccharides, destined to become N-linked sugars, are built
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Carbohydrates carry structural information:
Glycosylation at specific amino acid residues in proteins Checmial identity of carbohydrates in the polysaccharide chain Sequence of carbohydrate addition α- β-anomers Linkage through different OH groups Branching
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Lectin
is a cell surface receptor that recognize carbohydrates with a specificity brought about through multiple weak interactions
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Liver: Glucose monitor
removes excess glucose for storage as glycogen releases glucose to feed other tissues ensures enough glucose for other tissues (Brain/RBCs)
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Pancreas: glucose monitor
hormonally regulates glucose levels, releasing: insulin (when glucose is high) Glucagon (when glucose is low)
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Brain's primary fuel source is...
glucose
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RBCs only fuel source is...
Glucose
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Muscles: Glucose metabolism
use glucose as rapid energy source & store as glycogen
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Adipocytes: glucose metabolism
take up excess glucose to make fats
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What is the role of a glucose transporter (GLUT)?
to ensure that all tissues can take up a basal amount of glucose necessary for the cells to carry out their cellular functions
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GLUT 1 and GLUT 3
Found in all mammalian tissues Km = 1 mM Basal Glucose uptake
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GLUT 2
Found in liver and pancreatic ß cells Km = 15-20 mM removes excess glucose in the blood (liver) plays a role in regulation of insulin (pancreas)
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GLUT 4
Found in muscle and fat cells Km = 5 mM amount in muscle plasma membrane increases with endurance training
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Lower Km means...
higher in affinity
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Stages of Glycolysis
1. Trapping glucose in the cell and activation of glucose (req 2 ATP) 2. Splitting: cleaving one hexose; isomerization to yield 2 identical trioses 3. Harvesting: yields 4 ATP, 2 NADH, & 2 pyruvate
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Glycolysis: Stage 1 Getting ready to split glucose in two
Phosphorylation (req ATP) traps glucose in the cell and destabilizes glucose Reorganization ensures the aldose reaction yield is 2 trioses Further destabilization (req ATP) ensures a yield of 2 triose phosphates
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Stage 1 Glycolysis: Reaction 1
addition of phosphate group at C6 to trap glucose in the cell\ Enzyme Used: Hexokinase or Glucokinase The reaction favors the product so Hexokinase is regulated however, Glucokinase (found in liver) is not regulated. ![](https://encrypted-tbn3.gstatic.com/images?q=tbn:ANd9GcTyrIs44akBhWdD3Grr4MK1fC1LvlrkVDpV0JFfUPgNRjPnItqH)
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Glucokinase and Hexokinase
Under normal conditions, Hexokinase is used to phosphorylate glucose, but when concentration of glucose are high glucokinase will begin to pick up the glucose and phosphorylate Negative Effector: product inhibition (build up of G6P the molecule goes back and inhibits the enzyme that makes it)
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Stage 1 Glycolysis: Reaction 2
Isomerization of glucose 6 phosphate (G-6P) to fructose 6-phosphate (F-6P) Enzyme used: Phosphoglucose Isomerase
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Stage 1 Glycolysis: Reaction 3
essentially irreversible addition of phophate group to C1 (req 1 ATP) Enzyme Used: Phosphofructokinase (**_most __highly regulated_**) ![](http://www.mikeblaber.org/oldwine/BCH4053/Lecture34/glycolysis07.jpg)
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Phosphofructokinase 1 (PFK1)
sets the pace in glycolysis in liver and muscle Negative Effectors: High ATP/AMP, citrate, glucagon Positive Effectors: Low ATP/AMP, pH, F2, 6-BP, insulin
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Glycolysis: Stage 2 Step 1
Generating two 3-Carbon molecules (DHAP and GAP) Enzyme Used: Aldolase
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Glycolysis: Stage 2 Step 2
Isomerization of DHAP to GAP Enzyme Used: Triose Phosphate Isomerase
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Glycolysis: Stage 2 Step 3
Addition of Phosphate to C1 to form 1,3-BPG: high phosphate group transfer potential Enzyme Used: Glyceraldehyde 3-Phosphate Dehydrogenase
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Glycolysis: Stage 3 Step 1
Substrate level phosphorylation of ADP by 1,3-BP to form ATP and 3PG Enzyme Used: Phosphoglycerate Kinase
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Glycolysis: Stage 3 Step 2
Mutase rxn - moving the phosphate group from C3 to C2 (beta to alpha) Enzyme Used: Phosphoglycerate Mutase
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Glycolysis: Stage 3 Step 3
Dehydration, preparing to generate ATP Enzyme Used: Enolase
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Glycolysis: Stage 3 Step 4
Phosphoryl transfer to generate ATP and pyruvate Enzyme Used: Pyruvate kinase
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Pyruvate Kinase
Negative Effectors: Alanine, Glucagon, Phosphorylation Positive Effectors: F1, 6-BP, insulin
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Glycolysis Yield from one molecule of Glucose
Yield: 4 ATP, 2 NADH, 2 Pyruvate Consumed: 2 ATP, 2 NAD+
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