8.1 Metabolism Flashcards

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1
Q

Types of metabolic pathways

A
  1. Chains: glycolysis
  2. Cycles: Krebs
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2
Q

Types of enzymatic reactions

A
  1. Catabolic: free E released - exergonic
  2. Anabolic: E used - endergonic
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3
Q

Types of enzyme inhibition

A
  1. Reversible
  2. Irreversible

Depends on inhibitor

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4
Q

types of enzyme inhibitors

A
  1. Competitive: same active site as substrate
  2. Non-competitive: different active site to substrate
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5
Q

Competitive inhibition

A
  • binds to substrate’s active site
  • inhibitor chemically/syructurally similar to substrate
  • inhibitor’s effect can be decreased by increaseing substrate conc - likelihood od substarte binding instead of inhibitor increases
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6
Q

Non-competitive inhibitor

A
  • inhibitor binds to another site - allosteric site - not substrate active site
  • allosteric inhibitions leads to conformational enzyme changes - active site altered - substarte acnnot bind
  • increasing substrate conc would not decrease inhibitor effect
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7
Q

example of competitive inhibitor

A

Relenza drug - treat influenza virus

relenza competitively binds to neuraminidase active site - prevents docking proteins of virus - cells not infected

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8
Q

example of non-competitive inhibitor

A

Cyanide (CN) - poisonous

CN bonds to allosteric site in cytochrome oxidase in respiration - no longer pass e to final e acceptor O2 - electron transport chain cannot operate - cell dies

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9
Q

Explain feedback inhibition

A

Feedback inhibition (end-product inhibition): product binds to allosteric site reversibly - reaction halted - product levels drop - detach from allosteric site - recation procedes

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10
Q

Example of feedback inhibition

A

Threonine - osoleucine pathway (plants, bacteria): isoleucine synthesied from threonine - too much produced - inhibits production by binding to allosteric site in enzyme 1 - inhibition allows for both isoleucine and threonine exist in organism

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11
Q

Effects of different inhibitors in enzyme kinetics

A

Vmax can be reached with competitive inhibitor if conc of substrate is increased to high levels

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12
Q

Explain rational drug design vs screening in bioinformatic databases for Malaria treatment

A

Malaria caused by Plasmodium - two life cycles of Plasmodium - both in mosquito and human - development of parasite dtermined by enzymes - if inhibited - prevented from development

In bioinformatic databases potentail inhibitors are screend for parasitic enzyme inhibition - high efficinecy of finding a fit

_Rational drug desig_n (another method) - using computers to invent a chemical which would act as an inhibitor (anti-malarial drugs)

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13
Q

The accepted model of enzymes

A
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