Kaplan: Biochemistry: Chapter One Flashcards

1
Q

Where are amino acids found?

A

They are found in proteins.

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2
Q

What are alpha-amino acids?

A

Alpha-amino acids are those in which the amino group and the carboxyl group are bonded to the same carbon.

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3
Q

How the fuck do we know where the alpha-position is?

A

The alpha carbon will always be the carbon that is ADJACENT to the carboxyl carbon ( the carbon that is double-bonded to the oxygen AND bonded to the hydroxyl).

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4
Q

Describe the four groups that make-up an amino acid! GO

A

an amino (-NH2), the carboxyl group (-COOH), the hydrogen (H), AND the sidechain ( denoted R)

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5
Q

What makes each amino acid different from the other???

A

THE MF SIDECHAIN

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6
Q

Say it with me now!

A

STRUCTURE DETERMINES FUNCTION

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7
Q

True or False: Amino acids do not need to have the amino group and the carboxyl group attached to the same carbon. Explain why or why not.

A

This is obviously false babes… BECAUSE take methionine for example, the nitrogen is attached to the cyclic pentagon group but not attached to the alpha carbon.

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8
Q

Bitch is this true or false? Every amino acid found in the human body is specified by a codon in the genetic code or incorporated into proteins.

A

FALSE

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9
Q

What are we describing when we say proteinogenic amino acids???

A

There are various amino acids HOWEVERRR, there are 20 alpha-amino acids that the human body encodes.

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10
Q

Is glycine a chiral molecule?

A

NOSIREE! that bitch contains a hydrogen as its sidechain making two of the groups ze same.

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11
Q

Why is the amino group drawn on the left in Fischer projections?

A

The amino group is drawn to the left because all chiral amino acids used in eukaryotes are L-amino acids.

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12
Q

What is the configuration for all CHIRAL amino acids (not including glycine and cysteine)?

A

S-configuration

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13
Q

Which amino acid has an R-configuration?

A

Cysteine

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14
Q

What is a D-amino acid?

A

A D-amino acid is one in which the amino group is drawn to the right in a Fischer projection.

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15
Q

What does it mean to be non polar?

A

There is no overall charge.

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16
Q

What does it mean to be non-aromatic?

A

There is no hexagonal ring and there are no pi bonds.

17
Q

What are the seven amino acids that are non polar and non-aromatic?

A

glycine, alanine, valine, leucine, isoleucine, methionine, AND proline

18
Q

Which is the smallest amino acid?

A

The smallest amino acid is glycine

19
Q

Describe the sidechain of glycine

A

The sidechain of glycine is hydrogen which is why the amino acid is NOT chiral

20
Q

Describe the sidechain of alanine, valine, leucine, and isoleucine

A

They have alkyl side chains containing one to four carbons. Alkyl groups are alkane groups that are missing a hydrogen. CH4——–>CH3

21
Q

Describe the sidechain of methionine.

A

The sidechain of methionine contains a sulfur atom ( 1 of the 2 amino acids who have one) IN its sidechain

22
Q

Why is methionine considered non polar?

A

Even though it has a big fat sulfur atom in it, the methyl group keeps it relatively non-polar.

23
Q

Describe the sidechain of proline

A

It forms a cyclic amino acid, the amino nitrogen becomes a part of the side chain forming a five-membered ring.

24
Q

Describe the side chain of tryptophan

A

Tryptophan is the biggest of the aromatic group, it has a double-ring system and one of the rings contain a nitrogen giving this compound 2 nitrogen’s in its structure

25
Q

describe the sidechain of phenylalanine

A

This amino acid only has one benzyl ring ( meaning a benzene ring + a ch2 group)

26
Q

describe the sidechain of tyrosine

A

tyrosine’s sidechain sort of resembles phenylalanine but it has a hydroxyl group attached to the benzyl side chain

27
Q

How many amino acids are non-polar and non-aromatic?

A

seven

28
Q

How many amino acids have non-polar aromatic sidechains, what are they?

A

there are three of them, tryptophan, phenylalanine AND tyrosine

29
Q

How many amino acids have polar side chains? What are they?

A

There are five of them, serine, threonine, asparagine, glutamine, cysteine

30
Q

Describe the side chains of serine and threonine

A

Their side chains have a hydroxyl group which makes them POLAR AF and able to participate in hydrogen bonding, member NOF

31
Q

Describe the side chains of asparagine and glutamine

A

Their side chains have lovely amides ( -NH2 + double-bonded O on the same carbon) The amides do not become charged, leave those bitches alone

32
Q

How can you remember the difference between serine and threonine, structurally?

A

serine has one alkyl group (CH2) and threonine has one alkyl group ( CH3)

33
Q

Describe the side chains of cysteine

A

Cysteine is the other 1 of 2 aminos that have sulfur in its structure BUT the major difference is that the sulfur atom is bonded to a hydrogen which makes it a thiol

34
Q

What makes asparagine and glutamine structurally different?

A

Asparagine has one alkyl group (CH2) and glutamine has two alkyl groups ( CH2 x2)

35
Q

How many negatively charged (acidic) side chained amino acids? What are they?

A

There are two of them, aspartic acid AND glutamic acid. They anions are aspartate and glutamate, respectively.

36
Q

What are the three amino acids that have positively charges (basic) side chains

A

arginine, lysine, and histidine

37
Q

Which amino acids are hydrophobic and why?

A

The ones with long alkyl chains ( alanine, isoleucine, leucine, valine, and phenylalanine). They are most likely to be found in the interior of proteins.

38
Q

Which amino acids are hydrophilic and why?

A

All the amino acids with charged ( - or +) side chains are hydrophilic, these include arginine, histidine, lysine and the IONS aspartate and glutamate.