Metabolic Pathways Flashcards

1
Q

Where do you synthesize? (Anabolic)

A

Cytoplasm

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2
Q

Where do you break something down? (Catabolism)

A

Mitochondria

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3
Q

What is the substrate that starts and the product for Heme synthesis?

A

Succinyl -CoA is the substrate that starts (allosteric activator)

Ferrochelatase is the product which adds iron in the heme ring.

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4
Q

What amino acid and vitamin do you need for heme synthesis?

A

Glycine and Vit B6

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5
Q

If you are missing the mannose 6 phosphate label then no enzymes will end up in the lysosomes .. what DZ am I ?

A

I cell

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6
Q

Which complexes use heme ?

A

3 and 4

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7
Q

Statins destroy what?

A

Coenzyme Q10 aka ubiquinone

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8
Q

Copper is apart of which complex ?

A

complex IV aka cytochrome oxidase complex

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9
Q

Which complex phosphorlyates ?

A

Complex V

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10
Q

what blocks complex II ?

A

malonate

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11
Q

How do uncouplers cause Malignant hyperthermia and neuroleptic malignant syndrome?

A

allows ETC to continue but ATP synthesis stops and leaves muscle contracted

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12
Q

Which nucleotides have the tightest bond? loosest?

A

AT have the loosest bonds (double) and the most rapidly dividing cells

GC has the tightest (three) bonds and is found in the brain.

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13
Q

To isolate DNA use?

A

thymidine - southern blot

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14
Q

to isolate RNA use?

A

uracil - northern blot

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15
Q

What is the substrate that starts and the product for Purine synthesis?

A

Start with Ribose 5 phosphate from the Pentose Pathway

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16
Q

PRPP is high when?

A

de novo, higher Km

17
Q

PRPP is low when?

A

Salvage, lower Km

18
Q

When is de novo preferred?

A

periods of rapid growth

CA

0-2, 4-7, puberty, pregnancy

19
Q

rRNA are synthesized where?

A

nucleolus

they are most abundant

20
Q

mRNA

A

synthesized during transcription
DNA –> mRNA
3’ - poly A tail
5’ - Guanosine cap

21
Q

SNRPS - small nuclear ribonuclear proteins

A

smallest

responsible for splicing of mRNA during posttranscriptional modification

22
Q

tRNA is used in?

A

translation
the anticodon is responsible for finding AA
3’ contains CCA and cost 2 GTPs

23
Q

RNA polymerase 1 synthesizes

24
Q

RNA polymerase 2 synthesizes

25
RNA polymerase 3 synthesizes
tRNA and snRNP
26
enhancer, repressor
jump around from 1 chrom to another
27
if repressor mutated/ enhancer mutated
CA
28
When does cyanosis occur?
5g of Hg are fully desaturated of O2
29
Reasons for low reticulocyte count? (6)
renal failure aplastic anemia mets CA fanconi syndrome- pure RBC aplasia - 2nd possible thymoma diamond blackfan syndrome - RBC aplasia w/ finger abnormalities
30
tx for vWF
ADH analog - DDAVP Mod bleed - cryoprecipitate (F8,vWF, fibrinogen) severe bleed - FFP - F8 conc
31
Glanzmann thrombasthenia is due to ? Tx?
autoantibodies to gp2b/3a Tx: Gp2b/3a (TEA) Tirofiban Eptifabtide Abciximab
32
What can you give for intermittent claudication?
PDE III inhibitors: coronary vasodilator Cilastazole Dipyridamole
33
4 drugs for massive hemorrhage
Tranexamic acid F7 activator prothrombin complex fibrinogen complex
34
Catabolic Hormones
epinephrine glucagon cortisol growth hormone
35
What is the allosteric activator in glycolysis ?
F2,6DP which activates PFK1
36
What is the allosteric inhibitor in glycolysis ?
citrate
37
What happens when exercising in glycolysis?
PFK1 becomes too slow