Biochem MCQ 2019 Flashcards
In what organs Pentose Phosphate Pathway is a Major metabolic Pathway?
1)Mammary glands 2)Erythrocytes 3)Liver
Which of the following signaling molecules possess subunits in their structure:
- 1)PKC
- 2)PKA
- 3)Heterotrimeric G protein
- 4)Insulin receptor
- 5)EGF
2)PKA 3)Heterotrimeric G protein 4)Insulin receptor
Which of the following enzyme reactions is producing FADH2 and not NADH:
- 1)Alpha-ketoglutarate Dehydrogenase
- 2)Malate Dehydrogenase
- 3)Succinate Dehydrogenase
- 4)Isocitrate Dehydrogenase
3
Succinate Dehydrogenase produces FADH2.
Which of the following enzyme reactions is rate limiting step of the TCA cycle:
- 1)Alpha-ketoglutarate Dehydrogenase
- 2)Malate Dehydrogenase
- 3)Succinate Dehydrogenase
- 4)Isocitrate Dehydrogenase
4
Isocitrate Dehydrogenase is rate limiting step of the TCA cycle.
Substrates of Phosatidylserine Synthase 1 Enzyme:
- 1)Phosphatydilcholine
- 2)Phosphatydilethanolamine
- 3)CTP
- 4)Serine
- 5)ATP
- 6)DAG
- 7)CDP-DAG
1 , 4
Phosatidylserine Synthase 1:
Substrates: Phosphatydilcholine + Serine
Products: P-Serine + Choline
How many 2,3 BPG Molecules bind to the Tetramer Hemoglobin?
1
Phosphorylase Kinase:
1) Phosphorylates Glycogen Phosphorylase
2) Activates Glycogen Phosphorylase
3) Has Alpha, Beta, Gamma, Delta Subunits
4) Its Delta subunit is a Calmodulin.
5) Hydrolyzes the phosphate groups of Phosphorylase.
1 , 2 , 3 , 4
- Phosphorylase Kinase: Phosphorylates and Activates Glycogen Phosphorylase.
- Has Alpha, Beta, Gamma, Delta Subunits.
- Its Delta subunit is a Calmodulin.
Fructose Intolerance Cause?
Aldolase B deficiency
Why do you treat patients with tPA?
1) Protease that dissolves Fibrin.
2) Protease that converts Plasminogen to Plasmin.
3) it is no inhibited by plasma protease inhibitors.
4) Acts primarily in the location of Fibrin.
2 , 4
tPA is a protease that converts Plasminogen to Plasmin.
It acts primarily in the location of Fibrin.
What is the role of Hypertriacylglyceremia (HTG) in the development of Artherosclerosis?
HTG increases the shuttling of CETP (Cholesterol-ester transfer protein) HDL and VLDL with consequent formation of small dense LDL and Loss of HDL.
When Gla-domains are NOT formed in the blood coagulation proteins:
1) In Vit K - deficiency
2) In the presences of coumarin-derivatives
3) In the Liver disease when carboxylase cannot work
4) When in Hepatocyte, the epoxide reductase does not reduce vitamin K.
1 , 2 , 3 , 4
1) In Vit K - deficiency
2) In the presences of coumarin-derivatives
3) In the Liver disease when carboxylase cannot work
4) When in Hepatocyte, the epoxide reductase does not reduce vitamin K.
Unit of specific activity?
U/milligram
Lactose can be formed in a single step from:
1)Glucose 2)UDP-Galactose
In Partial Thromboplastin time (PTT) we learn about: 1)Factor VIII 2)Factor V 3)Factor X 4)Factor XII 5)Factor XI
1 , 2 , 3 , 4 , 5 Factor VIII, Factor XII, Factor XI -Belong to Intrinsic Pathway . Factor V and Factor X Belong to Common
True for Cori Cycle: 1) Liver takes up Lactate from Blood Circulation 2) Our body produces Lactate under resting conditions 3) Requires Energy 4) Links to types of tissues through the Circulation
1, 2 ,3, 4 1) Liver takes up Lactate from Blood Circulation 2) Our body produces Lactate under resting conditions 3) Requires Energy 4) Links to types of tissues through the Circulation
True for the formation of Malonyl-CoA: 1)Catalyzed by Citrate Lyase 2)Co-factor is Biotin 3)Negative feedback regulation by Palmitoyl-CoA 4)Regulated by Insulin and Glucagon 5)Requires ATP andBicarbonate
2 , 3 , 4 , 5 2)Co-factor is Biotin 3)Negative feedback regulation by Palmitoyl-CoA 4)Regulated by Insulin and Glucagon 5)Requires ATP andBicarbonate
Per Os administration of Uridine is a choice of treatment in case of: 1)UMP Synthase deficiency. 2)Orinithine transcarbamoylase deficiency. 3)Gout if allopurinol treatment causes orotic aciduria. 4)Solid tumers during 6-aza-uridine treatment.
1 , 2 , 3 , 4 -UMP Synthase deficiency. -Orinithine transcarbamoylase deficiency. -Gout if allopurinol treatment causes orotic aciduria. -Solid tumers during 6-aza-uridine treatment.
Aldolase B: 1)Cleaves F1,6BP 2)Cleaves F1P 3)Deficiency causes Essential Fructosuria 4)Deficiency causes Hereditary Fructose Intolerance 5)Symptoms of the deficiency are Hypoglycemia and Hyperuricemia.
1 , 2 , 4 , 5 Aldolase B cleaves mainly F1P. Deficiency causes Hereditary Fructose Intolerance and its Symptoms are Hypoglycemia and Hyperuricemia.
The binding of oxygen to Myoglobin relationship curve looks: 1)Sigmoidal 2)Linear - Positive 3)Linear - Negative 4)Hyperbolic
4 Hyperbolic
What is the “Induced fit” Concept: 1)Enzyme substrate binding induces an increase in the reaction entropy, therby catalyzing the reaction. 2)When a substrate binds to an enzyme the latter induces water loss. 3)Substrate binding may induce a Conformational change in the enzyme leading to better orientation of their functional groups 4)Enzyme specificity is induced by Substrate-Enzyme complex formation
3 Substrate binding may induce a Conformational change in the enzyme leading to better orientation of their functional groups
Which of the following lipoproteins doesn’t contain TAGs: 1)HDL3 2)HDL2 3)VLDL 4)Chylomicron
1) HDL3 HDL-Two ConTains TAGs
Choose the WRONG statement for Rynodine receptor: 1)its a Calcium channel 2)Has 4 subunits 3)It is the largest ion channel 4)Regulated by calmodulin 5)Same isoform for Heart and Skeletal Muscle
5 is Wrong! RYR1 - Skeletal Muscle RYR2 - Cardiac Muscle
Function of ABCA1 Transporter:
Pumps out cholesterol from extrahepatic tissue (to HDL)
True for the selectivity of Ion channel: 1)They can discriminate between identically charged ions. 2)They can only discriminate between Cations and Anions. 3)in Ca free media Ca channels become permeable for Na 4)Conserved P-loop Sequences determine selectivity of K, Na and Ca channels 5)Some ion channels are non-Selective.
1 , 3 , 4 , 5 -They can discriminate between identically charged ions. -In Ca free media Ca channels become permeable for Na -Conserved P-loop Sequences determine selectivity of K, Na and Ca channels -Some ion channels are non-Selective.
Open Probability is: 1)Total time spent open 2)Total observation time 3)Total time spent open/Total observation time 4)Total observation time/Total time spent open
3 Open Probability is:Total time spent open/Total observation time.
Which are True: 1)Glycolysis takes part in all humen cells. 2)the presence of oxygen is necessary for glycolysis 3)Pasteur effect is the phenomenon by which oxygen indirectly induces glycolysis 4)In mitochondrium containing cells end product of glycolysis is pyruvate 5)RBCs are capable of producing 4 mol of ATP from 1 mol of glucose.
1 , 4 Glycolysis takes part in all humen cells and In mitochondrium containing cells end product of glycolysis is pyruvate.
The induction of which proteins causes a decrease in the number of LDL receptors: 1)SRE 2)SREBP 3)SCAP 4)INSIG 5)IDOL
4 , 5 INSIG and IDOL are decreasing the number of LDLR, when induced by Insulin pathway and LXR respectively.
Isoelectric Point Defenition:
The pH at which a particular molecule carries no net electrical charge or is electrically neutral in the statistical mean
Which is NOT an electron carrier: 1)NAD 2)FAD 3)Biotin 4)Ubiquinone
3 Biotin is actually a Carboxyl-group carrier.
Which enzyme is not involved in Heme biosynthesis: 1) Heme Oxygenase 2) Aminolevulinic acid -Synthase 3)Aminolevulinic acid dehydratase 4)Urophorphyrinogen III Synthase 5)Urophorphyrinogen III Co-Synthase
1) Heme Oxygenase It is part of the Breakdown pathway.
Choose the enzymes induced by the Liver in Long term Starvation: 1) Aminotransferase 2) Phosphgluconate Dehydrogenase 3)Phosphenolpyruvate Carboxykinase (PEPCK) 4) Pyruvate Dehydrogenase 5) Malic Enzyme
1 , 3 Aminotransferase and PEPCK
Amino acids that enter the citric acid cycle as Alpha-Ketoglutarate: 1)Pro 2)Arg 3)Glu 4)Cys 5)Phe
1, 2 , 3 Amino acids that enter the citric acid cycle as Alpha-Ketoglutarate: Pro, Arg, Glu as well as His which is not asked.
Amino Acid without chiral Center
Gly
ABCG5 Function?
Pumps Cholesterol to Billiary Capillaries
Synthesized in the Zona Fasciculata of Adrenal Cortex: 1) Angiotensin II 2) Corticosterone 3) Cortisol 4) Angiotensinogen 5) Androstenedione
2 , 3 Corticosterone and Cortisol
Thrombomodulin effect on Blood coagulation: 1)Accelerates Activation of Protein C by thrombin 2)Inhibits fibrinogen conversion to Fibrin. 3)Activation of platelet by thrombin is inhibited by TM. 4)Inactivates Thrombin.
1 Thrombomodulin accelerates Activation of Protein C by thrombin. It changes Thrombin specificity and doesn’t act directly on none of the factors.
Which of the following conversions takes more than one step: 1)Alanine to Pyruvate 2)Glutamate to Alpha-Ketoglutarate 3)Aspartate to Oxaloacetate 4)Proline to Glutamate 5)Phenylalanine to Succinate
4 , 5 take more than one step. 1 ,2 ,3 are all transaminations carried by a single enzyme.
Major end product steroid hormone of Corpus Luteum:
Progesterone
What Statement is true for Insulin receptor substrate 1 (IRS1): 1)It is a Serine/Threonine kinase 2)It is a Phosphotyrosine docking protein 3)It binds to the Insulin receptor 4)Insulin receptor phosphorylates it on serine residues. 5)IP3 activates it.
2 It is a Phosphotyrosine docking protein.
True for the Dissolution of Fibrin: 1)Plasmin hydrolyzes the bonds between Fibrin monomers 2)Leukocytes participate in the process 3)Lys-Gln Isopeptide Cleavage occurs 4)Multiple peptide bonds within the fibrin monomers are hydrolyzed 5)A possible product is D-Dimer
2 , 4 , 5 2)Leukocytes participate in the process (Monocytes and Neutrophills) 4)Multiple peptide bonds within the fibrin monomers are hydrolyzed 5)A possible product is D-Dimer
Give at least 2 Cellular Elements Activating Glycogen Phosphorylase:
1) Calcium Signal 2) cAMP - PKA system 3) Phosphorylase Kinase
What is the dominant Electrophilic conjugation type in phase 2 Biotransformation:
Glutathione Conjugation
Type IIb (White) fibers : 1)has low glycogen content 2)has alot of capillaries 3)has low amount of mitochondria 4)Has high TAG content
3 Type IIb (White) fibers has low amount of mitochondria
Which of the following is NOT involved in Muscle contraction: 1)RYR 2)DHP 3)Nicotinic Ach Receptor 4)Beta receptor 5)L-type Calcium Channel
Beta receptors: They are part of the Sympathetic nervous system. All the rest take part in the Neuromuscular junction.
True for Transamination: 1) It is a reversible reaction 2) Co-factor for its enzymes is Pyridoxal Phosphate 3) First step is Ketoacid attaching to Lysine Residue of Enzyme forming a Schiff base 4)The Schiff base is in Tautomerism: equilibrium between Aldmine and Ketamine
All are true: 1) It is a reversible reaction 2) Co-factor for its enzymes is Pyridoxal Phosphate 3) First step is Ketoacid attaching to Lysine Residue of Enzyme forming a Schiff base 4)The Schiff base is in Tautomerism: equilibrium between Aldmine and Ketamine
Aminophenazone N-demythlation is catalyzed by: 1)Cytochrome Oxidaze 2)Catalase 3)CYP Isoenzyme 4)Superoxide dismutase 5)S-Adenosyl-Methionine
3 CYP Isoenzyme
Substrates of Phosatidylserine Synthase 2 Enzyme: 1)Phosphatydilcholine 2)Phosphatydilethanolamine 3)CTP 4)Serine 5)ATP 6)DAG 7)CDP-DAG
2 , 4 Phosatidylserine Synthase 2: Substrates: Phosphatydilethanolamine + Serine Products: P-Serine + Ethanolamine
Products of Oxidation of 3 moles of Glucose by the Pentose Phosphate Pathway?
3 Moles of Pentose 6 Moles of NADPH 3 Moles of CO2
What will increase in plasma due to the activity of Glucagon or ACTH?
Unesterified Fatty Acids
____ is a Primary bile acids formed by Hydroxylation, Side chain cleavage and Conjugation.
Taurocholic Acid is a Primary bile acids formed by Hydroxylation, Side chain cleavage and Conjugation.
Which enzyme will produce Dihydrotestosterone (DHEA) from Testosterone:
5-Alpha-Reductase
Inhibitor of Ribonucleotide Reductase: 1)Acyclovir 2)Methotrexate 3)araCTP 4)5-fuloro-deoxy-UMP
1 Acyclovir is a Reductase inhibitor
Roles of Nucleotides:
1) Hydrolysis of PP bound ATP to give energy. 2) DNA and RNA building blocks 3) act as Co-Enzymes 4) Second Messenger 5) Allosteric Effectors of Metabolic Processes
Orotic Aciduria is Caused by Deficiency of Enzymes in: 1)Epinephrine Synthesis 2)Purine Catabolism 3)Purine Synthesis 4)Pyrimidine Breakdown 5)Pyrimidine Synthesis (One Answer)
5) Pyrimidine Synthesis Bifunctional Enzyme UMP Synthase is Deficient. (Orotate Phosphorybosyl transferase + OMP Decarboxylase)
Choose the Substrates of PKA: 1)Glycogen Phosphorylase 2)Glycogen Synthase 3)Pyruvate Kinase 4)Hormone sensitive Lipase
ALL ! 1 , 2 , 3 , 4 -Glycogen Phosphorylase -Glycogen Synthase -Pyruvate Kinase -Hormone sensitive Lipase
True for 26S Proteasome: 1) Recognizes Misfolded proteins 2) Recognizes Ubiquitinated proteins 3) It is an ATPase 4) Beta subunits are the Catalytic ones 5) Alpha subunits are activators of Beta subunits
2 , 3 , 4 2) Recognizes Ubiquitinated proteins 3) It is an ATPase 4) Beta subunits are the Catalytic ones
Enzymatic Regulation of PDH Complex:
- PDH Kinase inactivates - PDH phosphatase activates
Which compound is substrate of Monoamine Oxidase: 1)Glutamate 2)Serotonin 3)Dopamine 4)Norepinephrine 5)Glutamine
2 , 3 , 4 Serotonin, Dopamine and NE are all metabolized by MAO.
Hyperuricemia will be the result of : 1)Glucose-6-phosphatase deficiency 2)HGPRT deficiency 3)Chemotherapy and Radiation therapy 4)PRPP-Amidotransferase Deficiency 5)Orotate-Phosphoribosyltransferase
1 , 2 , 3 Glucose-6-phosphatase and HGPRT deficiency. and Chemotherapy and Radiation therapy all cause an increase in Uric Acid in the Blood. (also in Mcardle disease)..
True for Enzymes: 1)Increase the equilibrium constant for a reaction, thus favoring the product formation 2)for effectivity they have to be equimolar to their substrates 3)They lower the activation energy for the reaction 4)They increase the stabillity of the product side. 5)Are never covalently attached to substrates or product.
3 They lower the activation energy for the reaction
Compounds or Enzymes of De-Novo Synthesis of AMP: 1)Ribose-5-Phosphate 2)Orotate 3)Aspartate carbamoyltransferase 4)Phosphrybosilformylgylcinamide synthetase 5)IMP
1 , 4 , 5 1)Ribose-5-Phosphate 4)Phosphrybosilformylgylcinamide synthetase 5)IMP (Orotate - Salvage , Asp carbamoyl… - Pyrimidines)
True for the results of Hypoxanthine-Guanine-Phosphoribosyl transferase deficiency:
1) Hypoxanthine is not converted to IMP
2) Hypoxanthine is not converted to GMP
3) Guanine is not converted to GMP
4) De-Novo Purine nucleotide synthesis is enhanced
5) Hyperuricemia develops
1 ,3 , 4 , 5 are True for HGPRT def . (Lesch nyhan): Hypoxanthine is not converted to IMP.
Guanine is not converted to GMP.
De-Novo Purine nucleotide synthesis is enhanced and Hyperuricemia develops.
Enzymes of Pyrimidine Salvage Reactions:
1) Thymine phosphribosyl transferase
2) Uridine-Cytidine Kinase
3) Deoxy-Cytidine Kinase
4) OMP Decarboxylase
1 , 2 , 3
1) Thymine phosphribosyl transferase
2) Uridine-Cytidine Kinase
3) Deoxy-Cytidine Kinase
Enzymes that catalyze the synthesis of long chain fatty acids in vertebrate cells (Pick one): 1)Are encoded in mitochondrial genes 2)Act as seven separate protein 3)Are part of a single polypeptide chain containing several distinct enzyme activities. 4)Are loclized in the mitochondrial matrix 5)None of the above
3 FA Synthase is a single polypeptide chain containing several distinct enzyme activities!
True for Kidney Cortex in starvation: 1)Glucagon activate Gluconeogenesis 2)Catecholamines activate Gluconeogenesis 3)Gluconeogenesis happens later than in Liver 4)There is high expression of Phosphofructokinase-1
2 , 3 Catecholamines activate Gluconeogenesis in the Kidney Cortex, this happens after a while in starvation - later than in Liver (pH dependent manner).
Synthesis of Tyrosine requires: 1)Phe 2)Phe Hydroxylase 3)Tetrahydrobiopterin 4)Dihydrobiopterin Reducatase 5)Alanine amino transferase activity in order to transform Phe to Phenyl-Pyruvate.
1 , 2 , 3 , 4 Synthesis of Tyrosine requires: Phe , Phe Hydroxylase, Tetrahydrobiopterin, Dihydrobiopterin Reductase.
Which of the following are Essential Amino Acids:
1) Ile
2) Ser
3) Cys
4) Phe
5) Trp
Isoleucine, Tryptophan and Phenylalanine are Essential amino acids.
How is Glycogen Phosphorylase is allosterically regulated:
1) Activated by AMP
2) Inhibited by ATP
3) Inhibited by AMP
4) Activated by ATP
5) Inhibited by Glucose
1 , 2 , 5
Glycogen Phosphorylase is allosterically Activated by AMP and allosterically Inhibited by Glucose and ATP.
Amino acids that are Ketogenic and Glucogenic:
1) Ile
2) His
3) Val
4) Arg
5) Tyr
1 , 5
Isoleucine and Tyrosine can form Ketone bodies as well as Glucose.
Glucagon regulation of Glycogen Storage (Pick One):
1) Simulates the Formation and Inhibits Breakdown 2)Inhibits the Formation and Stimulates the Breakdown 3)Inhibits Both Formation and Breakdown
4) Stimulates Both Formation and Breakdown
5) Stimulates Both Formation of Glycogen and Ketones
2
Glucagon inhibits the formation and stimulates the Breakdown
Amino acids with 4 carbons:
Asp , Asn ,Thr
Select the True statements:
1) Basic amino acids have net Positive charge at Neutral pH.
2) The Isoelectric point of basic amino acids is above 7 pH.
3) The Isoelectric point of the basic amino acids can be calculated as the average of their three pKa values.
4) Arg is a basic amino acid.
1 , 2 ,4 1)Basic amino acids have net Positive charge at Neutral pH. 2)The Isoelectric point of basic amino acids is above 7 pH. 4)Arg is a basic amino acid.
Are these two sentences true? Is there any connection? 1) Presynaptic Noradrenergic axon terminals retake up NE by Co-transport with Na. 2)NE re-uptake is decreased in Hypoxia.
Both sentences are True: Presynaptic Noradrenergic axon terminals retake up NE by Co-transport with Na (Secondary active transport). NE re-uptake is decreased in Hypoxia.(Na/K ATPase Low)
Glutamate is reduced to glutamic semialdehyde in the course of the formation of: 1)Proline 2)Ornithine 3)Glutamine 4)Glutathione 5)Gamma amino-butyrate
1 , 2 Glutamate is reduced to glutamic semialdehyde in the course of the formation of Proline and Ornithine.
In Fructose metabolism: 1)First step is a phosphorylation of fructose to F1P 2)First step is a phosphorylation of F1P to F1,6BP 3)First step is catalyzed by Fructokinase 4)All the same enzymes of glucose metabolism
1 , 3 First Fructose is converted to F1P by Fructokinase.
The accumulation of Citrate will: 1)Activate Glycolysis 2)Inhibit Glycolysis 3)No affect Glycolysis 4)Inhibit Gluconeogenesis
2 Inhibit Glycolysis
Which enzymes allows connection between the TCA cycle and Purine Nucleotide cycle: 1)Succinate Dehydrogenase 2)Citrate Synthase 3)PDH 4)Fumarase 5)Malate Dehydrogenase
4 , 5 - Malate Dehydrogenase and Fumarase: Fumarate coming from Adenylosuccinate lyase reaction can enter as malate to the mitochondrion and form oxlaoacetate.
True for HSL: 1)Activated in a cyclic AMP dependent manner. 2)Glucocorticoides induce transcription of the Enzyme. 3)Well-Fed induce transcription of the Enzyme. 4)Acts on the Surface of Endothelial Cells 5)Secreted by the Pancreas
1 , 2 are True for Hormone Sensitive Lipase. Activated in a cyclic AMP dependent manner. Glucocorticoides induce transcription of the Enzyme.
Which is the 30 Carbon Atoms Cholsterol precursor:
1) Isopernyl pyrophosphate
2) farnesyl pyrophosphate
3) Geranyl pyrophosphate
4) Squalene
5) Lithocholine
4
Squalene = 30 Carbons
Select the FALSE statement: 1)Arginine may be produced in the Kidney 2)Ornithine is synthesized from Glutamate 3)Nitrogen atoms in urea are derived from free ammonium ions and from Aspartate. 4)Urea can be produced in the Kidney.
4 is Wrong! Urea is produced in the Liver exclusively. only few parts of the urea cycle can occur in the kidney.
Pick the molecule that cannot go through the mitochondrial membrane: 1)Malate 2)Aspartate 3)Glutamate 4)Oxaloacetate
4 Oxaloacetate cannot go through the mitochondrial membrane.
UGT Enzyme location:
Endoplasmic Reticulum
Adenosine Deaminase reaction product:
Inosine
False for Nicotinic Receptors: 1)Activated by Ach 2)Linked to Myasthenia Gravis 3)Receptor Ion channel 4)Release Sodium only
4 Nicotinic AchR are releasing Na+ as well as K+
Which bases have an Amino-group in their structure: 1)Cytosine 2)Thymine 3)Uracil 4)Guanine 5)Adenine
1 , 4 , 5 -Cytosine -Guanine -Adenine
Cyclooxygenase:
1) Catalyses the conversion of Archidonate into Prostaglandins and Thromboxanes.
2) Inhibited by Aspirin
3) Hydrolyses the polyunsaturated fatty acid in SN2 position of Phopholipids
4) Is activated by indometacin
5) Inactivated in a Suicide Inhibition
1 , 2 , 5
Cyclooxygenases catalyse the conversion of Archidonate into Prostaglandins and Thromboxanes. Inhibited by Aspirin. Inactivated in a Suicide Inhibition
On which Lipoproteins ApoB-100 is found?
VLDL, IDL, LDL
Aspirin is used as a treatment for Myocardial infraction because:
It inhibits COX in Platelets.
Rate limiting step of Catecholamines synthesis: Enzyme, Co-factor, 3 Regulation ways
Tyrosine Hydroxylase Tetrahydrobiopterin regulated by: Ca++ and Phosphorylation which stimulate it. Norepinephrine cause negative feedback
Which is the unique enzyme expressed only in Zona Glomerulosa?
Aldosterone Synthase (18-Hydroxylase+Oxidase)
Pathways active in the Liver during Well-Fed state: 1)TAG Formation from FFA and Release of VLDL 2)Beta-Oxidation 3)Ketogenesis from Lactate 4)Lactate turning to Pyruvate and then to Acetyl-CoA 5)Lactate turning to Pyruvate and then to Oxaloacetate
1)TAG Formation from FFA and Release of VLDL 5)Lactate turning to Pyruvate and then to Oxaloacetate
Co-factors of Fatty Acid synthesis Pathway:
1)ACP 2)Biotin 3)NADPH
Typical Phase I reaction is : 1)Sulfatation 2)Glutathionation 3)Alklylation 4)Oxidation 5)Acetylation
4)Oxidation (or Hydroxylation) By Cytochrome P450 enzymes
Gilbert Syndrome is an unconjugated Hyperbillirubinemia just as ________ Syndrome.
Crigler - Nailar Syndrome
Correct ORDER for the enzymes of the De-Novo synthesis of Orotate: 1)Carbamoyl-Phosphate Synthase 2 2)Dihydroorotase 3)Asp transcarbmoylase 4)Dihydroorotate Dehydrogenase
1–>3–>2–>4 CPS2->Asp Transcarbomoylase->Dihydroorotase->Dihydroorotate Dehydrogenase
The Brain Prefers ___ but can use ___ as an energy source.
1) Glucose 2) Ketone Bodies
Results of 2,3BPG IN RBC’s ?
1) Glycolysis results in less ATP (2,3 BPG amount dependent) 2) Hemoglobin Binding - Oxygen release is Increased.
Carries most information on membrane topology of an ion channel: 1)Electromicroscopic image 2)The number and composition of subunits 3)Hydropathy plot 4)Molecular weight
3 Hydropathy plot Carries most information on membrane topology of an ion channel.
Consequence of inherited Adenosine Deaminase Deficiency?
Immunodeficiency
Serine, Alanine and Cysteine are all catabolyzed to form: 1)Alpha-Ketoglutarate 2)Succinate 3)Fumarate 4)Pyruvate 5)None of the above
4 Serine, Alanine and Cysteine are all catabolyzed to form: Pyruvate
Heparin is commonly used in treatment of Thrombosis because: 1)Inactivates Thrombin efficiently and directly. 2)Inhibits prothrombin activation by thrombin. 3)Facilitates thrombin inactivation by Antithrombin. 4)Enhances Plasmin efficiency.
3 Facilitates thrombin inactivation by Antithrombin.
Characteristics of Leptins: 1) These are Complex carbohydrates 2) Polypeptides produced by Adipocytes 3) There are types of obesities associates with their signal loss 4) Their production is proportional with the mass of Adipocytes. 5)High leptin level correlates to increased appetite.
2 , 3 , 4 Polypeptides produced by Adipocytes. There are types of obesities associates with their signal loss. Their production is proportional with the mass of Adipocytes.
Causes of Hyper-Homocysteine: 1)Lack of B6 2)Lack of B12 3)Enzyme Deficiency 4)Lack of Methionine
1 , 2 , 3 Lack of B6 or B12. Enzyme Deficiency - S-adenosylhomocysteinase. all cause Hyper-Homocysteine
Which deficiency could causes PKU: 1)Dihydrobiopterin reductase 2)Vitamnin B6 3)Phenylalanine Hydroxylase 4)Biopterin Synthesis 5)Vitamin C
1 , 3 ,4 Phenylalanine Hydroxylase - No outlet to Tyr Dihydrobiopterin reductase - No BH4 Co-factor Biopterin - No BH4 Co-factor
Which of the following is NOT common for FA Synthesis and Beta oxidation:
1) Acyl-CoA derivatives are intermediates
2) Double bonds are oxidized or Reduced by Pyrimidine nucleotide coenzymes.
3) These processes occur in Mito. Matrix
4) A derivative of Pantothenic acid is involved
3 is WRONG Beta oxidation happens in the mito. matrix while FA Synthesis in the Cytosol
True for synthesis of Norepinephrine:
1) Rate limiting step is Dopamine hydroxylase reaction 2)All pathway enzymes are located in NE axon terminal 3)Calcium activates Tyrosine Hydroxylase
4) Catechol-O-Methyltransferase doesn’t participate
3 , 4
In the synthesis of Norepinephrine:
Calcium activates Tyrosine Hydroxylase
Catechol-O-Methyltransferase doesn’t participate (COMT is for NE degradation)
The Ribosyl Phosphate needed for the synthesis of orotidylate, Inosinate and Guanylate is most directly provided by:
PRPP: 5-Phosphoribosyl-1-Pyrophosphate
True for Skeletal Muscle Lipid Metabolism:
1) LPL activity Increases in starvation
2) Synthesis of Ketone Bodies in starvation
3) In aerobic exercise conditions :Beta-Oxidation active
4) FA Oxidation - long term exercise energy supply
1 , 3 , 4
LPL activity Increases in starvation (Only in Muscle)
3) In aerobic exercise conditions : Beta-Oxidation active
4) FA Oxidation - long term exercise energy supply
In De-Novo Pyrimidine Synthesis which of these Enzymes is involved:
1) Adenine Phosphoribosyl transferase
2) Glutamine Phosphoribosyl-pyrophosphate amidotransferase
3) Orotic Acid Phosphoribosyl transferase
4) Hypoxanthine-Guanine Phosphoribosyl Transferase
5) Cytosine Phosphoribosyl Transferase
3
Orotic Acid Phosphoribosyl transferase is part of De-Novo Pyrimidine Synthesis.
Amino Acids with 2 Chiral Centers:
Threonine and Isoleucine
The amino acid that is released into the bloodstream by the muscle:
1) Trp
2) Val
3) Ala
4) Leu
The amino acid that is released into the bloodstream by the muscle Alanine.
Which CYPs are not participating in Aldosterone synthesis from Cholesterol: 1)Scc 2)17 Hydroxylase 3)2 Hydroxylase 4)Aromatase
2 , 4 17 Hydroxylase and Aromatase are not involved in Aldosterone synthesis.
Disease caused by Clc channel mutation: 1)Meysthenia 2)Myotonia 3)Epilepsy 4)Cystic fibrosis 5)Long QT syndrome
2 Myotonia
Order of Enzymes of Cateocholamines Synthesis (5+Cofactors):
- Tyrosine Hydroxylase
- Dopamine - Beta Hydroxylase
- Phenylalanine Hydroxylase
- DOPA Decarboxylase
- Phenyl-Ethanolamine-N-Methyltransferase
1) Phenylalanine Hydroxylase (BH4)
2) Tyrosine Hydroxylase (BH4)
3) DOPA Decarboxylase (PLP)
4) Dopamine - Beta Hydroxylase (Vit C/Ascorbate)
5) Phenyl-Ethanolamine-N-Methyltransferase (SAM)
Proteins participating in Reverse cholesterol transport:
1) ApoA1
2) LCAT
3) AopB48
4) ApoC2
5) LPL
1 , 2
ApoA1 activates LCAT - Esterifying Cholesterol
What Enzyme of the Glycolysis forms GTP?
None
Select the true statements: 1)Cholesterol is formed from HMG-CoA synthesized in the Mitochondria 2)Cholesterol is formed from HMG-CoA synthesized in the Cystosol 3)Mevalonatel is formed from HMG-CoA Carboxylation 4)NADPH is needed for Mevalonate Synthesis 5)Production of isopentenyl-pyrophoshate also requires a decarboxylase
2 , 4 , 5 2)Cholesterol is formed from HMG-CoA synthesized in the Cystosol 4)NADPH is needed for Mevalonate Synthesis 5)Production of isopentenyl-pyrophoshate also requires a decarboxylase
What binds the Sodium-Potassium ATPase on the outer membrane side:
1) Ouabain
2) Na+
3) K+
4) ATP
1 , 3
Ouabain and K
Squalene synthesis from farnesyl pyrophosphate results in the release of two moles of PPi for each Squalene. This is part of the Synthesis of:
1) Cholesterol
2) Pyrimidine
3) Pentose Phosphate Pathway
1) Cholesterol
Squalene synthesis from farnesyl pyrophosphate results in the release of two moles of PPi for each Squalene.
True for AMPK Phosphorylation in the muscle (Pick one):
1) Activates Glycogen Phosphorylase
2) Catalyzes F2P conversion to F2,6BP
3) Inactivates ACC thus decreases Malonyl-CoA con.
4) inactivates PDH - TCA Cycle inhibited 5)Activates FA Synthesis
3) Inactivates ACC thus decreases Malonyl-CoA con. More oxidizing less producing Fat Acids. gotta get those ATPs.
In the conversion of dUMP to dTMP the Methyl group donor is:
1) SAM
2) N5-N10-Methylyene Tetrahydrofolate
3) N5-Methyl Tetrahydrofolate
4) Tetrahydrofolate
2) N5-N10-Methylyene Tetrahydrofolate
Which of the following are involved in the uptake of cholesterol originating from peripheral tissues:
1) LDLR
2) Scavenger receptor A
3) Scavenger receptor B1
4) LXR
5) ABCA1
1 , 3
Scavenger receptor B1 and LDLR
In one cycle of Beta oxidation how many ATP would be formed?
1 NADH and 1 FADH2 formed will give off together: 4 ATP Molecules (2.5+1.5)
Which amino acid has the derivative of Melanin?
Tyrosine
All of the following are gluconeogenic enzymes, EXCEPT: 1)F1,6BPase
2) G6Pase
3) PK
4) PC
5) PEPCK
3
Pyruvate Kinase is Glycolytic.
What is the dominant Nucleophillic conjugation type in phase 2 Biotransformation:
Glucuronic acid Conjugation
What is the treatment for Hyperammonemia?
Sodium Phenylbutyrate and Sodium Benzoate. Both are alternative Nitrogen carriers - Mixed to form Lactulose. (Also low Protein diet).
True for Hemoglobin:
1) It is a tetramer
2) The Fe2+ moves into the plane of the heme on oxygenation.
3) The subunits have low affinity (T) state and High affinity in (R) State.
4) Bisphosphoglycerate stabilizes the R-form.
1 , 2 ,3
Hemoglobin is a tetramer, It’s Fe2+ moves into the plane of the heme on oxygenation. The subunits have low affinity (T) state and High affinity in (R) State.
Glutathione Reductase in RBC:
1) NADH Increase
2) H2O2 Increase
3) Removal of H202
4) Inhibits PPP
5) Reducing Glutathione for Glutathione Peroxidase reaction.
3 , 5 Glutathione Reductase in RBC: Removal of H202 + Reducing Glutathione for Glutathione Peroxidase reaction.
Balance of ATP Formation/Consumption of Anaerobic Glycolysis:
2 ATP consumed and 4 ATP formed
What is the committed step of of cholesterol biosynthesis?
HMG-CoA Reduction to Mevalonate by HMG-CoA Reductase.
Which of the following is a Proton pump in the Electron transport chain:
1) Ubiquinone
2) Complex II
3) Complex I
4) Cytochrome C
3
Complex I is a Proton Pump, the rest are simply passing along the Electrons
(Complex II = Succinate Dehydrogenase)
What are the two distinct activities of the Debranching Enzyme?
1) alpha-1-6 Glucosidase, Debranching Activity
2) Transferase Activity
In Prothrombin time assay (PT) we can learn about : 1)Factor VII 2)Factor V 3)Factor X 4)Factor XII 5)Factor XI
1 , 2 , 3 Factor VII, Factor V, Factor X - Belong to Extrinsic Pathway.
What is the common when Reaction when Hypoxanthine is converted to Xanthine and when Xanthine is converted to Uric Acid? Name the enzyme!
Oxygenation!
Xanthine Oxidase creates these Purine degredation products Hypoxanthine - 1 Oxygen Xanthine - 2 Oxygens Uric Acid - 3 Oxygens
False one for Ion channels:
1) Select among identically charged ions
2) Saturate at High ion concentration
3) Throughput rate approaches the Diffusion limit.
4) Transport Ions with their hydration shells
4 Ion channels mimic the Hydration shell while transfer the Ions without it.
What are the two basic Precursors forming Heme? Enzyme of the first step of the pathway?
Glycine and Succinyl-CoA
ALA Synthase
Treatment for Parkinson Disease (Pick one - Major)):
1) L-DOPA
2) MAO-B inhibitors
3) Peripheral Decarboxylase Inhibitors
4) Dopamine receptor agonists.
3
Treatment for Parkinson Disease is Peripheral Decarboxylase Inhibitors
True for StAR protein:
1) It is a Cholesterol Carrier
2) It promotes the cleavage of the 21-OH group
3) It promotes the cleavage cholesterol side chain with P450 which is found on the ER membrane.
4) It promotes the cleavage cholesterol side chain with P450 which is found in the Mitochondria.
1 , 4
It is carrying cholesterol into the close by Mitochondrion and therefore promoting its chance to be cleaved by CYP responsible for Side chain cleavage (Scc).
In Prothrombin time assay (PT) we can learn about : 1)Fibrinogen
2) Prothrombin
3) Factor VIII
4) Factor IX
5) Factor XI
Only 1 and 2!
PT checks the Extrinsic and Common pathway.
3 , 4 ,5 are Intrinsic Pathway.
Which are NOT classified as Ketone bodies : 1)Dihydroxyacetone 2)Acetoacetate 3)Beta-Hydroxybutyrate 4)Alpha-Hydroxybutyrate 5)Oxaloacetate
1 , 4 , 5 Dihydroxyacetone, Alpha-Hydroxybutyrate and Oxaloacetate are NOT Ketone bodies.
Perquisite for Thromboxane synthesis are:
1) Availability of phospholipid containing arachidonate for PLA2
2) Active Lipooxygenase
3) Functional COX
4) Corticosteroids do not inhibit COX
1 , 3 , 4
Availability of phospholipid containing arachidonate for PLA2, Functional COX, Corticosteroids do not inhibit COX are all needed for TXA2 formation.
What is the Location of Glucose-6-Phosphatase Enzyme:
Glucose-6-Phosphatase is on Endoplasmic reticulum
What is the basis of time-dependent changes in membrane permeability ?
Opening of discrete protein pores aka Ion Channels
Give at least 3 Functions of LXR:
1) Positive regulation of ABCA1 Transporter (also General cells)
2) Positive Regulation of CYP7A1 Enzyme (In the Liver)
3) IDOL All working to Reduce cellular Cholesterol Conc.
Which of the following provides Nitrogens to form Nucleotides: 1)Amido-groups of Gln 2)Amino-groups of Glu 3)Aspartate 4)Glycine 5)NH3
1 , 3 , 4 Amido-groups of Gln, Aspartate and Glycine are all providing Nitrogens for Nucleotide formation.
Are these sentences true? Is there any interrelation between them? 1)Hypertriglyceridemia favors the progression of Atherosclerosis. 2)The Cholesteryl-Ester transfer protein shuttles between HDL and VLDL , as well as between VLDL and LDL exchanging triacylglycerols for cholesterol esters.
Both are true: 2 )leads to 1)
Happens after 3 days of starvation:
1) Glutamine is released from the liver will be higher than Glutamate intake.
2) Glutamine is taken by the Kidney
3) Glutamine is taken by the Liver
4) Muscles will release a large amount of Amino acid
2 , 4 -
True after 3 days of starvation Glutamine is taken by the Kidney Muscles will release a large amount of Amino acid
What receptor in the CNS functions as a Na and Ca Channel?
NMDA
Threonine Dehydratase: Substrate, Product and Coenzyme.
Threonine Dehydratase: Substrate - Threonine Product - Alpha-ketobutyrate + Ammonia Coenzyme -PLP
Why Coumarol is an antithromobotic drug?
-Inhibits Vit K reduction thus preventing incorporation of gamma-Carboxyglutamate into prothrombin (and other Factors with Gla domain )
Function of NPC1L1 Transporter:
Pump in cholesterol into Epithelial Intestinal cells.
How many unitary charges allows activation of VDC?
12 -16
Possible utilization of Glucose in Erythrocytes (at least 2):
1) Anaerobic Glycolysis
2) Pentose Phosphate Pathway
3) Glucouranate Pathway
True for Nicotinic Ach receptor:
1) It is a Homopentamer, it dysfunction can lead to myasthenia.
2) It is a Heteropentamer, it dysfunction can lead to myasthenia.
3) It is a Tetramer, its dysfunction can lead to myotonia. 4)The ligand binding domain is a 4 fold symmetrical gating ring.
5) The ligand binding domain is a 5 fold symmetrical ring.
2 , 5
It is a Heteropentamer, it dysfunction can lead to myasthenia. The ligand binding domain is a 5 fold symmetrical ring.
Treatments for symptoms of Antiphospholipid syndrome:
1) Vit K
2) Vit K anatagonists
3) Folic Acid
4) Antifolates
5) Heparin
6) Protamine
2 , 5
Vitamin K antagonists and Heparin
Looking at a Lineweaver plot, If the enzyme linear function changed with inhibition in a way that Vmax and Km are lower, which inhibition occurred?
Uncompetitive inhibition decreases Vmax and Km.
Pituitary hormone promoting the conversion of cholesterol to Progenenolone in the gonads:
LH - Lutenizing Hormone
4 general types of Phase I reactions in Biotransformation:
1)Oxidation 2)Reduction 3)Hydrolysis 4)Hydration
Von Gierke Disease is caused by deficiency of : 1)Glycogen Synthase 2)Glycogen Phosphorylase 3)Glucose-6-Phosphatase 4)UDP-Glucose-Uridylyl transferase
3) Glucose-6-Phosphatase Deficiency. It is a glycogen storage disease when one cannot simply break down Glycogen = Accumulation, Lactic Acidosis, Hypoglycemia are the symptoms.
The synthesis of Purines and Pyrimidines differs in:
Purine synthesis starts with the formation of PRPP, whereas Pyrimidines incorporate the PRPP near the end of the Pathway.
In the Respiratory chain, ATP Synthase is inhibited by: 1)Oligomycin 2)Statins 3)Barbiturates 4)Cyanide
1 In the Respiratory chain, ATP Synthase is inhibited by Oligomycin.
Which is FALSE for starvation: 1)Kidney Glutaminase level is elevated 2)Glucagon activates Gluconeogenesis in the Kidney 3)Glutamine is a Glucose precursor in the kidney 4)Glucagon activates Gluconeogenesis in the Liver
2 Glucagon is not activating Gluconeogenesis in the Kidney but Catecholamines do.
In the Respiratory chain, Complex IV is inhibited by: 1)Oligomycin 2)Statins 3)Barbiturates 4)Cyanide
4 In the Respiratory chain Complex 4 is inhibited by Cyanide.
While in starvation state the Liver has an active: 1)Glut 2 2)Acetyl-CoA carboxylase 3)Hexokinase 4)PFK2
1 While in starvation state the Liver has an active Glut 2
10 ml of 0.1M Arg solution (starting from fully protonated form) is titrated with 0.1 N NaOH. At which of the NaOH additions do you expect buffer formation:
1) 5ml
2) 10ml
3) 15ml
4) 20ml
5) 25ml
1 , 3 , 5
5 , 15 and 25 ml will yield a Buffer solution.
Since 10, 20 , 30 ml will be the Eq points - Buffering in between them.
Its Eq point signfys the de-portonation of 1 functional group - 3 for Arg.
True for Neurons metabolism (MCQ):
1) The importance of PPP in neurons is negligible.
2) have Highly active Gln Synthase.
3) They are extremely sensitive to oxygen depletion.
4) Gln could be used as energy source.
5) Able to produce and consume Lactate.
3 , 4 , 5 are true for Neuron metabolism.
- They are extremely sensitive to oxygen depletion.
- Gln could be used as energy source.
- Able to produce and consume Lactate.
True for Ribonucleotide Reductase (MCQ):
1) Thioredoxin acts as an essential electron carrier
2) There is a separate enzyme for: ADP, CDP, GDP, UDP
3) Mechanism involves formation of Free Radical
4) Acts on Nucleotide Diphosphates
5) Glutathaione is Part of the Electron transfer
1 , 3 , 4 , 5
1) Thioredoxin acts as an essential electron carrier
3) Mechanism involves formation of Free Radical
4) Acts on Nucleotide Diphosphates
5) Glutathaione is Part of the Electron transfer
What is the difference in the Negative Feedback regulation of Hexokinase and Glucokinase?
Glucokinase is not inhibited back by G6P while Hexokinase Does. (But by Fructose 6 phosphate)
Which of Urea Cycle enzymes are located in the Mitochondria:
1) CPS1
2) Ornithine transcarbamoylase
3) Argininosuccinate Lyase
4) Argininosuccinate Synthetase
5) Arginase
1 , 2
Carbamoyl Phosphate Synthetase 1 (CPS1) and Ornithine transcarbamoylase are found in the Mitochondria.
SAM is a Methyl Donor in the Synthesis of:
1) Carnitine
2) Creatine
3) Choline
4) Epinephrine
All of them!
1)Carnitine 2)Creatine 3)Choline 4)Epinephrine
FALSE for Fatty Acid Elongation System (Pick one):
1) In SER
2) uses Malonyl-CoA
3) Produces Steroyl-CoA from Palmitoyl-CoA
4) Direct Precursor of Added Carbons is Acetyl-CoA
5) It involves same four step sequence of FA Synthase
4
Direct Precursor of Added Carbons is Acetyl-CoA
Give us GABA Shunt:
1) Ketoglutarate
* -Ketoglutarate DH*
2) Glutamate
* -Glutamate DH*
3) GABA
* -GABA Transaminase*
4) Succinate Semialdehyde
* -Succinate Semialdehyde DH*
5) Succinate
Are these two sentences true? Is there any connection?
1) Dopamine-Beta-Hydroxylase is localized in vesicles of noreadrenergic axons
2) Dopamine is formed in synaptic vesicles
1 is true but 2 is false.
Dopamine-Beta-Hydroxylase is localized in vesicles of noreadrenergic axons, this is why Noradrenaline is formed in synaptic vesicles.
Which Amino acids are purely Ketogenic?
Leucine and Lysine
What is the fate of the 1’ Carbon in Pentose Phosphate Pathway?
Becomes CO2
True for Alpha-2-Plasmin Inhibitor:
1) One of the most efficient (endo) protease inhibitors
2) It forms equimolar complex with plasmin leading to activity loss
3) Fibrin-bound plasmin is an easier target for it
4) It is bound to fibrin by FXIII
1 , 2 , 4
1) one of the most efficient (endo) protease inhibitors
2) It forms equimolar complex with plasmin leading to activity loss
4) It is bound to fibrin by FXIII