Metabolic Concepts Flashcards

1
Q

End product of aerobic glycolysis

A

Pyruvate

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2
Q

End product of anerobic glycolysis

A

Lactic acid

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3
Q

Precursor for FA and cholesterol

A

Acetyl CoA

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4
Q

Parent compound of steroid hormones

A

Cholesterol

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5
Q

Provide carbon skeletons for AA synthesis

A

Pyruvate and TCA intermediates

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6
Q

Source of reducing equivalents like NADPH

A

Pentose phosphate Pathway

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7
Q

Source of ribose for DNA synthesis

A

Pentose phosphate pathway

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8
Q

Majority of AA metabolism involves this reaction/process

A

Trans-Amination

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9
Q

Co enzyme needed for trans-amination

A

Pyridoxal phosphate

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10
Q

LARGEST lipo-protein

A

Chylomicron

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11
Q

Major difference between triclycerides in chylomicrons and VLDL

A

VLDL typically contains endogenously secreted triglycerides

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12
Q

Biochemical pathways that occur both in the cytosol and mitochondria

A

Heme synthesis,
Urea Cycle
Gluconeogenesis

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13
Q

Biochemical pathways that occur in the mitochondria

A

FA Oxidation (B oxidation)
Acetyl CoA production
TCA cycle
Oxidative phosphorylation

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14
Q

Major biochemical pathways that occur strictly in the CYTOPLASM

A
FA Synthesis 
Glycolysis 
Pentose phosphate pathway
Cholesterol synthesis 
Steroid synthesis (SER)
Protein synthesis (RER)
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15
Q

The only 2 mechanisms how fats in the diet can be converted to glucose

FAT —?—> Glucose

A

Odd chain fatty acid via Propionyl CoA

Glyerol from Triglycerid breakdown

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16
Q

Primary substrate/metabolic intermediate for gluco-neo-genesis

A

Oxalo-Acetate

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17
Q

ONLY pathways available in RBCs

A

Anaerobic glycolysis

Pentose phosphate pathway

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18
Q

Term used to describe metabolic pathways that act as link between anabolic and catabolic pathways

A

Amphibolic-TCA cycle

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19
Q

Equation used to compute for the concentration of weak acid and its conjugate base

A

Henderson Hasselbalch Equation

pH = pKa + log [unprotonated/protonated]

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20
Q

Smith-Lemli-Opitz syndrome

A

7 dehydro-cholesterol reductase deficiency

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21
Q

Enzyme responsible for phosphorylating glucose in the liver and pancreatic Beta cells
High km, high vmax
Induced by insulin,
NOT inhibited by glucose 6 phosphate feedback

A

Gluco-kinase

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22
Q

Enzyme from Glycolysis, Gluconeogenesis, or BOTH:

Pyruvate kinase

A

Glycolysis

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23
Q

Enzyme from Glycolysis, Gluconeogenesis, or BOTH:

Phospho-fructo-kinase 1

A

Glycolysis

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24
Q

Enzyme from Glycolysis, Gluconeogenesis, or BOTH:

Phospho-fructo-kinase 2

A

Glycolysis

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25
Enzyme from Glycolysis, Gluconeogenesis, or BOTH: | Hexokinase
Glycolysis
26
Enzyme from Glycolysis, Gluconeogenesis, or BOTH: | Phospho-glycerate kinase
BOTH Glycolysis Gluco-neo-genesis
27
Enzyme from Glycolysis, Gluconeogenesis, or BOTH: | Fructose 1 6 bis-phosphatase
Gluco neo genesis
28
Enzyme from Glycolysis, Gluconeogenesis, or BOTH: | Glucose 6 phosphatase
Gluco neo genesis
29
Phosphoenol pyruvate carboxy-kinase
Gluco neo genesis
30
RLE of TCA cycle
Iso-citrate dehydrogenase
31
RLE of de novo PYRIMADINE synthesis
CPS-2 | Carbamoyl Phosphate Synthase 2
32
RLE of urea cycle
CPS 1 | Carbamoyl Phosphate Synthase 1
33
Positive allosteric regulator of Urea cycle and its RLE
N Acetyl Glutamate
34
RLE of de novo PURINE synthesis
Glutamin PRPP Amido-transferase
35
RLE of ketogenesis
HMG CoA synthase
36
Predominant type of estrogen and source menopausally
Adipose tisse estr-ONE
37
Most important pathway for cholesterol excretion
Excretion through the bile
38
``` Which is NOT a mono-saccharide Glycerol Glucose Galactose Fructose ```
Glycerol
39
``` Which is NOT a disaccharide Lactose Sucrose Maltose Amylose ```
Amylose
40
Backbone of sphingomyelin
Ceramide
41
Name the essential amino acids (9)
Histidine, Methionine, Iso-leucine, Leucine, Lysine, Phenylalanine, Threonine, Tryptophan, and Valine.
42
Apo-lipo-protein that mediates remnant re-uptake
APO-E
43
Apo-lipo-protein that activates lipo-protein lipase
APO-C2
44
Apo-lipo-protein that binds to the LDL receptor
APO-B100
45
Name secondary protein structures
``` Sheets Helices Bends Turns Loops ```
46
Proteins that assist other proteins in the proper folding into their secondary structures and prevents aggregation
Chaperone proteins
47
Neurological dse resulting from - mis-folding and accumulation of protein B amyloid and - reduction in acetyl-choline activity in the brain
Alzheimer's Dse
48
Syndrome characterized by kinky hair and growth retardation. Reflects a deficiency of the copper which is required by lysyl oxidase, which catalyzes formation of the covalent cross links that strength collagen fibers
Menke's syndrome
49
What are the hematologic adaptations to high altitude
Increase: - RBCs - Hemoglobin - 2,3 BPG
50
Metabolic pathway involved in the synthesis of 2,3- BPG
Luebering Rapoport Shunt
51
LDH-1 and LDH-5 are enzymes used as biomarkers in the
Heart (LDH 1) | Liver (LDH 5)
52
Cariac biomarker for MI that appears - Within 4-6h of MI - 24h Peak - 48-72 back to Baseline
CK MB
53
Newborns with Hyaline membrane disease are deficient in
Di-Palmitoyl Phospha-tidyl-choline
54
21st AA present in the active site of glutathione peroxidase and deiodinase and other enzymes
Seleno-Cysteine
55
Porphobilinogen de-aminase deficiency | + associated with predominant skin manifestations
Acute intermittent porphyria
56
MC subtype of porphyria and cause by deficiency of uro-por-phrynogen decarboxylase
Porphyria cutanea tarda
57
Anti-oxidant vitamins
Vit A Vit C Vit E
58
Alcoholic man with blurring of vision, muscle weakness, incoordination, altered sensorium, dementia should be given what vitamin
Thiamine
59
What does digestion of starch stop in the stomach
Acid pH deactivates salivary amylase
60
MOA of tetano-spasmin
Cleaves synapto-brevin --> preventing GABA release