Term 1- Lec 1&2- AA, pH, and Proteins Flashcards

1
Q

Which AA’s are Non-Polar

A

Glycine, Alanine, Leucine, Isoleucine, Valine, Methionine, Phenylalanine, Proline, Tryptophan

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2
Q

Which AA’s are Uncharged Polar

A

Serine, Threonine, Tyrosine, Glutamine, Asparagine

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3
Q

Which AA’s are Acidic Charged Polar

A

Glutamic Acid (Glutamate), Aspartic Acid (Aspartate)

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4
Q

Which AA’s are Basic Charged Polar

A

Histidine, Arginine, Lysine

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5
Q

Functional Group and Interactions of Glycine

A

Hydrogen (achiral). Hydrophobic interactions

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6
Q

Functional Group and Interactions of Alanine

A

Methyl. Hydrophobic interactions

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7
Q

Functional Group and Interactions of Leucine

A

Branched chain hydrocarbon. Hydrophobic interactions

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8
Q

Functional Group and Interactions of Isoleucine

A

Branched chain hydrocarbon. Hydrophobic interactions

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9
Q

Functional Group and Interactions of Valine

A

Branched chain hydrocarbon. Hydrophobic interactions

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10
Q

Functional Group and Interactions of Methionine

A

Contains S. Hydrophobic interactions

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11
Q

Functional Group and Interactions of Phenylalanine

A

Contains an Aromatic Ring. Hydrophobic interactions

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12
Q

Functional Group and Interactions of Tryptophan

A

Contains an Aromatic Ring. Hydrophobic interactions

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13
Q

Functional Group and Interactions of Proline

A

Is an Imino Acid. Hydrophobic interactions

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14
Q

What is the difference Methionine and Tryptophan from the rest of the Non-Polar AA’s?

A

They both contain a polar atom, but the polarity is masked by the surrounding hydrocarbons

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15
Q

Functional Group and Interactions of Serine

A

Hydroxyl. Hydrogen Bonding

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16
Q

Functional Group and Interactions of Threonine

A

Hydroxyl. Hydrogen Bonding

17
Q

Functional Group and Interactions of Tyrosine

A

Hydroxyl. Hydrogen Bonding

18
Q

Functional Group and Interactions of Glutamine

A

Carboxamide (-CONH2). Hydrogen Bonding

19
Q

Functional Group and Interactions of Asparagine

A

Carboxamide (-CONH2). Hydrogen Bonding

20
Q

Functional Group and Interactions of Cysteine

A

Sulfhydryl. Hydrogen Bonding and Disulfide Bonding

21
Q

Functional Group and Interactions of Glutamic Acid (Glutamate)

A

Carboxyl Group. Ionic Bonding and Hydrogen Bonding

22
Q

Functional Group and Interactions of Aspartic Acid (Aspartate)

A

Carboxyl Group. Ionic Bonding and Hydrogen Bonding

23
Q

Functional Group and Interactions of Histidine

A

Basic Groups. Ionic Bonding and Hydrogen Bonding

24
Q

Functional Group and Interactions of Arginine

A

Basic Groups. Ionic Bonding and Hydrogen Bonding

25
Functional Group and Interactions of Lysine
Basic Groups. Ionic Bonding and Hydrogen Bonding
26
Equation for pH
pH = -log( [H+] )
27
Equation for Ka
Ka = ( [H+] • [A-] ) / [HA]
28
Equation for pKa
pKa = -log( Ka )
29
Henderson-Hasselbach Equation
pH = pKa + log( [A-] / [HA] )
30
pH = pKa
50/50 [A-] & [HA]
31
pH = pKa - 1
91% HA
32
pH = pKa + 1
91% A-
33
1º protein structure
AA sequence
34
2º protein structure
∂-helices, ß-sheets, and Loops
35
3º protein structure
Protein folding. Hydrophobic interactions and Covalent/Non-covalent bonding
36
4º protein structure
Multiple polypeptide chains binding together to form the subunits of one active protein
37
Super 2º structure- name and description
Motifs. Recognizable folding patterns involving 2+ 2º structures. i.e. ß-barrel
38
Why are super 2º structures not 3º structures?
Motifs do not hold their structures by themselves. They require 3º structure to remain motifs.