Amino Acid Groups and Bonds

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31 Terms

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Nonpolar, Aliphatic R groups

  • Glycine, Gly, G

  • Alanine, Ala, A

  • Proline, Pro, P

  • Valine, Val, V

  • Leucine, Leu, L

  • Isoleucine, Ile, I

  • Methionine, Met, M

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Aromatic R groups

  • phenylalanine, Phe, F

  • Tyrosine, Tyr, Y

  • Tryptophan, Trp, W

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Polar, Uncharged R groups

  • Serine, Ser, S

  • Threonine, Thr, T

  • Cysteine, Cys, C

  • Asparagine, Asn, N

  • Glutamine, Gln, Q

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Positively Charged R groups

  • Lysine, Lys, K

  • Histidine, His, H

  • Arginine, Arg, R

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Negatively Charged R groups

  • Aspartate, Asp, D

  • Glutamate, Glu, E

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Hydrogen Bonds

  • when 2 closely spaced EN atoms share a proton

    • EN atom: partial negative

    • proton: partial positive

  • N,O,F

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Hydrophobic interactions

  • stabilize bimolecular structure

  • has the hydrophilic heads and the hydrophobic tails

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2 reasons why non-polar groups avoid interaction with water

  1. can’t H bond to water, so when in water, they reduce the number of H bonds water can make (UNFAVORABLE CHANGE IN ENTHALPY)

  2. water molecules on their surface become highly ordered (UNFAVORABLE CHANGE IN ENTROPY)

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4 Types of non-covalent interactions

  1. H bonds

    1. b/w neutral groups

    2. peptide bonds

  2. Ionic Interactions

    1. attraction

    2. repulsion

  3. Hydrophobic Interactions

  4. Van der Waals: 2 atoms close in proximity

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Structure of an Amino Acid

  • Amino Group

  • Carboxyl Group

  • H

  • R group

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Residue

  • single building block (monomer) in a polymer

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Glycine

  • Gly, G

  • nonpolar, aliphatic

<ul><li><p>Gly, G</p></li><li><p>nonpolar, aliphatic </p></li></ul><p></p>
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Alanine

  • Ala, A

  • Nonpolar, aliphatic

<ul><li><p>Ala, A </p></li><li><p>Nonpolar, aliphatic </p></li></ul><p></p>
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Proline

  • Pro, P

  • Nonpolar, aliphatic

<ul><li><p>Pro, P</p></li><li><p>Nonpolar, aliphatic </p></li></ul><p></p>
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Valine

  • Val, V

  • nonpolar, aliphatic

<ul><li><p>Val, V</p></li><li><p>nonpolar, aliphatic </p></li></ul><p></p>
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Leucine

  • Leu, L

  • nonpolar, aliphatic

<ul><li><p>Leu, L</p></li><li><p>nonpolar, aliphatic </p></li></ul><p></p>
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Isoleucine

  • Ile, I

  • nonpolar, aliphatic

<ul><li><p>Ile, I</p></li><li><p>nonpolar, aliphatic </p></li></ul><p></p>
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Methionine

  • Met, M

  • nonpolar, aliphatic

<ul><li><p>Met, M</p></li><li><p>nonpolar, aliphatic </p></li></ul><p></p>
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Phenylalanine

  • Phe, F

  • Aromatic

<ul><li><p>Phe, F</p></li><li><p>Aromatic </p></li></ul><p></p>
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Tyrosine

  • Tyr, Y

  • Aromatic

<ul><li><p>Tyr, Y </p></li><li><p>Aromatic </p></li></ul><p></p>
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Tryptophan

  • Trp, W

  • Aromatic

<ul><li><p>Trp, W</p></li><li><p>Aromatic </p></li></ul><p></p>
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Serine

  • Ser, S

  • Polar, uncharged

<ul><li><p>Ser, S</p></li><li><p>Polar, uncharged </p></li></ul><p></p>
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Threonine

  • Thr, T

  • Polar, uncharged

<ul><li><p>Thr, T</p></li><li><p>Polar, uncharged </p></li></ul><p></p>
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Cysteine

  • Cys, C

  • Polar, uncharged

  • can form disulfide bonds

    • covalent bonds between 2 cysteine residues

  • Polar, uncharged

<ul><li><p>Cys, C</p></li><li><p>Polar, uncharged </p></li><li><p>can form disulfide bonds</p><ul><li><p>covalent bonds between 2 cysteine residues </p></li></ul></li><li><p>Polar, uncharged </p></li></ul><p></p>
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Asparagine

  • Asn, N

  • Polar, uncharged

<ul><li><p>Asn, N</p></li><li><p>Polar, uncharged </p></li></ul><p></p>
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Glutamine

  • Gln, G

  • Polar, uncharged

<ul><li><p>Gln, G</p></li><li><p>Polar, uncharged</p></li></ul><p></p>
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Aspartate

  • Asp, D

  • Neg charge

<ul><li><p>Asp, D</p></li><li><p>Neg charge</p></li></ul><p></p>
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Glutamate

  • Glu, E

  • Neg charge

<ul><li><p>Glu, E</p></li><li><p>Neg charge </p></li></ul><p></p>
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Lysine

  • Lys, K

  • Pos charge

<ul><li><p>Lys, K</p></li><li><p>Pos charge </p></li></ul><p></p>
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Histidine

  • His, H

  • Pos charge

<ul><li><p>His, H</p></li><li><p>Pos charge </p></li></ul><p></p>
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Arginine

  • Arg, R

  • Pos Charge

<ul><li><p>Arg, R</p></li><li><p>Pos Charge</p></li></ul><p></p>