Protein Structure and Function Flashcards

1
Q

order/sequence of the amino acids in a protein; involve peptide bonds

A

Primary protein structure

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2
Q

takes shape of alpha helix or beta pleated sheet, held by hydrogen bonds

A

Secondary protein structure

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3
Q

3-D- contains 1 polypeptide chain in backbone

A

Tertiary protein structure

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4
Q

multiple polypeptide chains called subunits

A

Quaternary protein structure

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5
Q

What are the 3 feat of a peptide bond ?

A

planar
restricted mobility
R group in trans config

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6
Q

Acidosis features? (4)

A

hyperkalemia
Kussmaul breathing
increase GABA
denature proteins

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7
Q

determines types of AAs in protein but not sequence

never tell how many Asp and Glu are in protein

A

acid hydrolysis

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8
Q

good only for prolines - turn yellow

all other AAs turns purple

A

Ninhydrin reaction

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9
Q

only accurate up to 100 AAs

uses phenyl isothiocyanate as reagent

A

Edman’s degradation

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10
Q

What does Mercaptoethanol do?

A

break disulfide bonds

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11
Q

CNBr cuts to the ____ of ____?

A

right of MET

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12
Q

Aminopeptidase cuts the ___ of___?

A

right of the amino-terminal amino acid

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13
Q

What restriction peptidase cuts to the right of GLY, ALA, and SER ?

A

Elastase

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14
Q

Chymotrypsin cuts to the ___ of ___?

A

right of PHE, TRP, TYR

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15
Q

What AAs are examples of alpha helix?

Hint: coiled or spiral conformation
My Locks/Curls = Good Hair (MLC GH)

A
MET
LYS
CYS
GLU
HIS
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16
Q

What AAs are examples of Beta pleated sheet?

Hint: Flat
I enVy TiTs

A

ISO
TYR
TRP
VAL

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17
Q

Proteins are made by? Examples?

A

BM- Immunoglobins

Liver (90%) - albumin, fibrinogen, alpha 1 antitrypsin

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18
Q

Procalcitonin tests what?

A

Excess protein in the serum during infxn.

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19
Q

What shows a falsely high ESR?

A

anemia

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20
Q

What shows a falsely low ESR?

A

sickle cell anemia, polycythemia

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21
Q

When do you run a SED rate ?

A

FUO - fever of unknown origin

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22
Q

In an Autosomal Dominant what is the % if one parent has it?

If both parents have it?

A

50% if one

75% if both

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23
Q

have the gene but doesn’t have the dz

A

incomplete penetrance

24
Q

family members have the gene and the dz but all look different

A

variable expresssion

25
Autosomal Dominant Dz involve ?
structural proteins
26
Primary amyloidosis feat? (2) | Seen in which persons?
decrease compliance of BVs = less distensibility BV more likely to rupture if BP increases Young person with no h/o of HTN; intracerebral hemorrhage
27
Secondary amyloidosis is due to
chronic inflammatory dz
28
AA amyloid
A=acute phase reactants/inflammatory dz developing countries - chronic infxn developed countries - RA, SLE, IBD
29
AB amyloid
Age/ Downs related Alzheimer dz
30
AB-2 aka Beta 2 macroglobulin amyloid
Chronic renal failure
31
AE and AF: MEN -II
Endocrine | Familial
32
AL- Multiple Myeloma
ALight chains - MM | Kappa>Lambda
33
Transthyretin
amyloid assoc w/ aging senile plaque MCC of hereditary familial amyloidosis AD
34
Example of Tertiary structures consisting mostly of Alpha helixs?
Hb | intermediate filaments
35
Example of Tertiary structures consisting mostly of Beta pleated sheets?
fatty acid transporters or antibodies
36
Example of Tertiary structures consisting mostly of alpha and beta pleated sheets?
some enzymes
37
Rate limiting enzymes (allosteric enzyme) have what type of structure?
Quaternary
38
1st order elimination
constant fraction/ proportion % eliminated per hr
39
if the substrate concentration no longer affect vmax
zero order elimination
40
zero order elimination
metabolizing a constant number rather than a fraction
41
Why is it better to keep the drug at first order?
Drug can be broken down then
42
Drugs that are acids and charged go to what organ?
kidney - for water soluble compounds
43
Drugs that are fat soluble go to what organ?
liver
44
2 alpha - 2 betas
HbA -adult
45
2 alpha - 2 gamma
HbF - fetal
46
2 alpha - 2 delta
HbA2 ..2%
47
How to induce HbF in pt ?
Hydroxyurea wipes BM - HbF is expressed
48
What shifts the O2-Hb dissociation curve to the right ?
``` increase CO2 ACID 2-3DPG EXCERCISE TEMP ```
49
What are 3 adaptations of hypoxia?
Polycythemia - increase EPO Increase mitochondrial density increased angiogenin
50
Dz's that wipe out the bone marrow can cause what ?
Massive Splenomegaly - Spleen does work of BM | any myelofibrosis disorder
51
5 pathways in the mitochondria and cytoplasm ? HUG - Family Now
``` HEME SYNTHESIS UREA CYCLE GLUCONEOGENESIS FATTY ACID SYNTHESIS PYRIMIDINE SYNTHESIS ```
52
MCC of oxidized iron
Sulfa drugs Anti-malarial Metronidazole INH
53
MCC of IDA in 20-40
IBD
54
MCC of IDA in >40y/o
mucosal bleeding
55
Tx for IDA
ferrous sulphate
56
Labs for IDA Serum Fe ? Saturation? Ferritin ?
Serum Fe - Low Saturation - Low Ferritin -Low Transferritin - High