Amino Acids Flashcards

(25 cards)

1
Q

What functional groups does the basic amino acid structure have?

A
  • Amino
  • Hydrogen
  • Carboxylate group
  • Side chain (R)
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2
Q

Which 5 amino acids are charged?

A
  • Aspartate (-)
  • Glutamate (-)
  • Arginine (+)
  • Lysine (+)
  • Histidine (+)
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3
Q

What are Aspartate’s abreviations, structure, side chain, etc.?

A
  • Asp, D
  • pKa of 3.9
  • Net negative charge at pH 7
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4
Q

What are Glutamate’s abreviations, structure, side chain, etc.?

A
  • Glu, E
  • pKa of 4.1
  • Net negative at pH 7
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5
Q

What are Lysine’s abreviations, structure, side chain, etc.?

A
  • Lys, K
  • pKa of 10.5
  • net positive at pH 7
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6
Q

What are Arginine’s abreviations, structure, side chain, etc.?

A
  • Arg, R
  • pKa of 12.5
  • Net positive charge at pH 7
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7
Q

What are Histidine’s abreviations, structure, side chain, etc.?

A
  • His, H
  • pKa of 6.0
  • The imidazole ring in His can be either positively charged or neutral depending on the environment
  • Its ability to bind with different metals helps us with purification of proteins
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8
Q

What are hydrophilic amino acids?

A
  • Serine
  • Theronine
  • Cysteine
  • Asparagine
  • Glutamine
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9
Q

What are Asparagine’s abreviations, structure, side chain, etc.?

A
  • Asn, N
  • Found on the surface of globular proteins
  • Able to form hydrogen bonds
  • Hydrophilic
  • Similar to Aspartate
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10
Q

What are Glutamine’s abreviations, structure, side chain, etc.?

A
  • Gln, Q
  • Can form numerous hydrogen bonds
  • Hydrophilic
  • Structurally similar to Glutamate
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11
Q

What are Serine’s abreviations, structure, side chain, etc.?

A
  • Ser, S
  • Hydroxyl group in Ser forms hydrogen bonds and can be a substrate in proteins for kinase-mediated phosphorylation
  • Hydrophilic (a bit hydrophobic from the CH2 center)
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12
Q

What are Threonine’s abreviations, structure, side chain, etc.?

A
  • Thr, T
  • Similar to Ser because of the hydroxyl group
  • Hydroxyl group can form hydrogen bonds and may be phosphorylated by kinases
  • Hydrophilic
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13
Q

What are Cysteine’s abreviations, structure, side chain, etc.?

A
  • Cys, C
  • Ionizable side chain has pKa 8.3
  • Sulfhydryl can form disulfide bonds with other Cysteines (redox reaction) and they can form weak hydrogen bonds
  • Only L-amino acid with an absolute configuration of R
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14
Q

Which amino acids can become phosphorylated and what allows this to happen?

A
  • Kinases are enzymes that add a phosphate group to a protein
  • This commonly occurs with Ser and Thr
  • Phosphatase can then take the phosphate group off the protein
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15
Q

Which amino acids are hydrophobic?

A
  • Glycine
  • Alanine
  • Proline
  • Valine
  • Leucine
  • Isoleucine
  • Methionine
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16
Q

What are Glycine’s abreviations, structure, side chain, etc.?

A
  • Gly, G
  • The smallest amino acid
  • The most chemically neutral aa due to the hydrogen side chain
  • Hydrophobic
17
Q

What are Alanine’s abreviations, structure, side chain, etc.?

A
  • Ala, A
  • Very abundant in proteins
  • Minimally hydrophobic
18
Q

What are Proline’s abreviations, structure, side chain, etc.?

A
  • Pro, P
  • Cyclic ring limits the conformations that the proline can adopt
  • Backbone nitrogen lacks a hydrogen which limits hydrogen bonding
  • Hydrophobic
19
Q

What are Valine’s abreviations, structure, side chain, etc.?

A
  • Val, V
  • Found in the hydrophobic core of globular proteins
  • Small hydrophobic amino acid
20
Q

What are Leucine’s abreviations, structure, side chain, etc.?

A
  • Leu, L
  • The most abundant amino acid in proteins
  • Promotes hydrophobic interactions in the core of globular proteins
  • Hydrophobic
21
Q

What are Isoleucine’s abreviations, structure, side chain, etc.?

A
  • Ile, I
  • Found close to leucine and other hydrophobic amino acids
  • Hydrophobic
22
Q

What are Methionine’s abreviations, structure, side chain, etc.?

A
  • Met, M
  • The sulfur in Met is unreactive
  • Always the starting amino acid
    • Recognition amino acid
23
Q

What are Phenylalanine’s abreviations, structure, side chain, etc.?

A
  • Phe, F
  • Phenyl ring is hydrophobic and chemically inert
  • Good signaling amino acid
  • Aromatic ring
24
Q

What are Tyrosine’s abreviations, structure, side chain, etc.?

A
  • Tyr, Y
  • Ionizable hydroxyl griup is pKa 10.1
    • It forms hydrogen bonds making Tyr an amphipathic amino acid
  • Absorbs light at 280 nm
  • Aromatic
25
What are Tryptophan's abreviations, structure, side chain, etc.?
* Trp, W * Trp is the largest amino acid * Strongly absorbs light at 280 nm (this will help us measure the concentration measurements due to the absorption of light) * Aromatic