lecture 4 Flashcards

1
Q

describe essential amino acids for humans

A

humans can produce 9 amino acids
other essential ones need to be obtained from food
failure to obtain leads to degradation of body, because body does not store amino acids (like with fats/starch)
plants also synthesis amino acids

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2
Q

what are conditional essential amino acids?

A

they are not essential
except for when ill, stress or deficient
includes arginine, cysteine, glutamine, tyrosine, glycine, ornithine, proline, and serine

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3
Q

what is a amino acid that humans make but plants cant

A

selenocysteine
it is a better nucleophile then Cys cause has a smaller pKa
is a amino acid found in proteins

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4
Q

what is selenoenzyme + what is its function

A

proteins made of selenocysteine that has catalytic activity.

  • Peroxide removal
  • Reduction of thioredoxins
  • Selenophosphate synthesis
  • Activation + inactivation of thyroid hormones
  • Repair of oxidised Met in protein
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5
Q

common characteristics of amino acids

A
  • Tetrahedral alpha carbon
  • Carboxyl group
  • Hydrogen bound to alpha carbon
  • Side chain (varies)
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6
Q

describe amino acids at pH 7

A
  • At pH 7
    ○ Amino group has pos. Charge
    ○ Carboxyl group has neg. Charge
    ○ Zwitterion
    • When more acidic environment- add a protein, gives a overall pos. Charge
      • When go into a basic environment- loss a protein, gives a overall neg. Charge
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7
Q

what is pKa

A

pH at which 50% of ion has dissociated is pKa

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8
Q

describe non-polar amino acids

A
  • Ala, Val, Leu are important in maintaining 3D structure, due to clustering away from water
  • Proline is cyclic, induces abrupt change in direction of polypeptide chain
  • MET, Trp, Phe, Iie are important for processes that drive peptide chains to fold, due to hydrophobic water-excluding properties
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9
Q

describe uncharged amino acids

A
  • Gly, Ser, Asn, Gln
  • Except for glycine, contains a side chain which can form a hydrogen bond with water
  • Glycine cant form H bonds because of simple H-R groups
  • Its solubility in influenced by polar amine + carboxyl groups, therefore grouped as polar
  • Glycerine- very small, so can fit into niches
  • Thr, Cys, Tyr- more insoluble in water than non-polar amino acids
    -Play a variety of nucleophilic roles in enzyme reactions
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10
Q

describe acidic amino acids

A
  • R-groups contain a carboxyl group (weak acids)
  • Exist as COO- at pH 7, so neg. Charge
  • Involved in binding metal ions
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11
Q

describe basic amino acids

A
  • Lys, Arg, His
  • Net pos. Charge at pH 7
  • Lys + arg fully protonated at pH 7
  • His only 10% protonated at pKa 6.4
  • His also has important role as proton donors + acceptors in enzyme reactions
  • Arg + lys involved in electrostatic interactions in protein
  • Biological buffers
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12
Q

amino acids that are rare in proteins

A
  • Hydroxylysine + Hydroxyproline- found in connective tissue proteins (collagen + gelatine)
  • G-Carboxyglutamate acid- found in blood clotting proteins
  • Pyroglutamate acid- found bacteriorhodopsin
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13
Q

describe amino acid spectrophotometric properties

A
  • No amino acids absorb visible lights
  • All amino acids absorb infared however
  • Determine protein conc. By measuring absorbance at 280nm
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14
Q

describe the stereochemistry of amino acids

A
  • L and R
    • Only L-isomer of amino acids occur commonly in nature
    • All amino acids BUT glycine are chiral (all amino acids have 4 different groups attached to the alpha carbon)
    • R, S nomenclature is superior, since amino acids like isoleucine + threonine (has 2 chiral centers), named unambigously
      ○ Chiral centers
      § Is an atom that has 4 different groups bonded to it in such a manner, htat it has a non-superimposable mirror image
    • 2 possible configurations (enantiomers)
    • Emantiomers are observed to rotate polarised light in either clockwise or counterclockwise direction (optical activity)
      ○ D configuration = to the right
      ○ L configuration = to the left
    • All amino acids from proteins are in the L configuration
      Some amino acids have more chiral carbons
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15
Q

describe the thalidomide case

A
  • In germany, 1957
    • Marketed as a sedative with few side effects for pregnant women to avoid morning sickness
    • But when given, some it was in S and some was R enantiomers
    • S- teratogenic
      R- effective sedative
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