Basic Science MT 1 Biochem Flashcards

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1
Q

9 AA with NONPOLAR side chains

A

Glycine
Alanine
Valine

Leucine
Isoleucine
Methionine
Proline

Phenylalanine
Tryptophan

“GAV LIMP PT”

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2
Q

Non-polar AA with secondary amino group. May be referred to as “Imino Acid”

A

Proline

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3
Q

Are non polar AA hydrophobic or hydrophilic?

A

hydrophobic

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4
Q

Which NONPOLAR amino acid can contribute to a DISULFIDE bond?

A

Methionine

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5
Q

Which nonpolar amino acid is OPTICALLY INACTIVE?

A

Glycine

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6
Q

Which nonpolar AA is used to form SEROTONIN?

A

Tryptophan

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7
Q

List 6 AA with UNCHARGED polar side chains

A

Glutamine
Asparagine
Serine

Cysteine
Threonine
Tyrosine

“GAS CTT”

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8
Q

Which amino acid with an UNCHARGED polar side chain is used to form dopamine?

A

Tyrosine

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9
Q

List the 2 AAs with ACIDIC side chains

A

glutamate

aspartate

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10
Q

List 3 AAs with basic side chains

A

Histidine
Arganine
Lysine

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11
Q

Are all AAs found in proteins in people of the D or L configuration?

A

L

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12
Q

In sickle cell anemia, the AA ____ is substituted for the glutamate at the 6th position in the beta subunit of Hb.

A

Valine

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13
Q

In hemoglobin C disease, the AA ___ is substituted for glutamate at the 6th position in the beta subunit of Hb.

A

Lysine

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14
Q

The sequence of AAs in a protein is referred to as the ____ structure of a protein

A

Primary

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15
Q

Alpha helix, beta sheets, and beta bends are examples of the ____ structure of a protein.

A

Secondary

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16
Q

The 3D shape of a folded protein is referred to as the ___ structure of a protein.

A

Tertiary

17
Q

Arrangement of MULTIPLE POLY-PEPTIDE subunits in the protein are referred to as the ____ structure of a protein.

A

Quaternary

18
Q

Primary, secondary, tertiary, and quaternary structure all contribute to the ____ of the protein

A

Native Conformation

19
Q

Specialized groups of proteins named ____ are required for PROPER FOLDING of some nascent peptides.

A

Chaperones

20
Q

Unfolding and disorganization of the protein’s secondary and tertiary structure is referred to as ____ of the protein

A

Denaturing

21
Q

Misfolding of proteins and abnormal tau proteins, may result in amyloids and neurofibrillary tangles, which are characteristics of ___ disease.

A

Alzheimer’s Disease

22
Q

An altered version of a prion protein can cause a group of diseases known as TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES (TSEs). An example in humans is ___ disease.

A

Creutzfeldt-Jakob disease

23
Q

In proteins, AAs are joined covalently by ___ bonds, which are AMIDE linkages between the alpha carboxyl group of one AA and the alpha AMINO group of another.

A

Peptide

24
Q

Hemoglobin ___ is the major Hb in adults. It is comprised of 2 ____ and 2 ____ chains. Hb can carry ___ oxygen molecules.

A

HbA
alpha globin
beta globin
4

25
Q

Myoglobin is a hemeprotein present in ____ and _____ muscle. Myoglobin can reversibly bind ___ oxygen molecule.

A

Heart
Skeletal
1

26
Q

Draw + Label the Oxygen Dissociation Curve for Hb +Mb

A

XX

27
Q

The Mb oxygen dissociation curve is described as ____. The Hb oxygen dissociation curve is described as ____.

A
Mb = hyperbolic
Hb = sigmoidal
28
Q

Cooperative binding of oxygen by the four subunits of hemoglobin means the binding of an oxygen molecule at one heme group ___ the affinity for oxygen of the remaining heme groups in the same Hb molecule.

A

INCREASES

29
Q

With the ___ effect, release of oxygen from Hb is enhanced when the pH is ____ and the pCO2 is _____. This is also described as a shift to the ___ of the oxygen dissociation curve.

A

Bohr effect
pH = lowered
pCO2 = increased
shift = Right

30
Q

Lungs have a ___ pH, tissues have a ____ pH

A
lungs = higher
tissues = lower
31
Q

Carbon monoxide shifts the ODC to the ___, thus DECREASING the ability of Hb to release oxygen to tissues.

A

Left

32
Q

Hb ___ is the major Hb found in the fetus and newborn. Fetal Hb has a ___ affinity for oxygen compared to HbA.

A

HbF

greater affinity

33
Q

Increased amounts of Hb ___ are found in RBCs of patients with diabetes mellitus. This type of Hb is described as ____ Hb

A

Hb A1C

Glycosylated

34
Q

_____ is a hereditary HEMOLYTIC DISEASE in which an imbalance occurs in the synthesis of globin chains of Hb.

A

Thalassemia

35
Q

____ is the most abundant protein in the body and includes 3 alpha chains which form a TRIPLE HELIX.

A

Collagen

36
Q

____ is a group of CONNECTIVE TISSUE DISORDERS, which result in fragile, stretchy and loose joints.

A

Ehler’s Danlos Syndrome

37
Q

____ is a group of CONNECTIVE TISSUE DISORDERS, which result in BONES THAT EASILY BEND AND FRACTURE.

A

Osteogenesis Imperfecta

38
Q

Alpha 1-Antitrypsin prevents ELASTIN DEGRADATION in the ____ walls. A deficiency of alpha 1-antitrypsin can cause a lung disease called ____.

A

alveolar walls

emphysema

39
Q

Mutations in the fibrillin-1 protein are responsible for ____ Syndrome

A

Marfan