Ch3: Important Molecules Flashcards

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1
Q

Amino Acids: Nonpolar, Hydrophobic

A
glycine
alanine
valine
methionine
leucine
isoleucine
proline
phenylalanine
tryptophan
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2
Q

Amino Acids: Polar, Neutral

A
serine
threonine
asparagine
glutamine
cysteine
tyrosine
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3
Q

Amino Acids: Polar, Acidic

A

aspartic acid

glutamic acid

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4
Q

Amino Acids: Polar, Basic

A

histidine
arginine
lysine

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5
Q

why is the structure of proline unique

A

proline has a ring in the side group. this ring is responsible for causing kinks in secondary structures; therefore, it is never seen in alpha-helix of protein structures.

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6
Q

Diasteriomers

Epimers

A

non-superimposable, non-mirror image
Ex: D-glucose and D-galactose (different configuration at stereocenter 4)
to be more accurate, D-glucose and D-galactose are epimers(diastereomers differing in configuration at only one steroecenter)

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7
Q

Enantiomers

A

non-superimposable mirror images
molecules that are exactly the same except one will have an R absolute configuration at a stereo center and the other molecule will have an S configuration at the stereocenter

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8
Q

difference between absolute configuration designation and optical activity designation

A

absolute configuration: R or S
optical activity: D or L (dextro/levoROTATORY)
configuration doesn’t predict optical activity

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9
Q

number of possible steroisomers

A

2^n where n=# of sterocenters

*be mindful of meso

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10
Q

anomer

A

subclass of diastereomer. Epimers are non-superimposable, non-mirror images that differ at only one stereocenter. Anomers are simply that ring form of an epimer.
Ex: Epimer-linear glucose
anomer-ring glucose

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11
Q

pyranose

A

six member sugar ring, five carbons with one oxygen ether bond

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12
Q

furanose

A

5 membered ring; four carbons, one oxygen ether

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13
Q

anomeric carbon

A

the carbon on a ringed sugar molecule that was the victim of nucleophilic attack by the deprotonated oxygen

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14
Q

difference between alpha and beta sugars

A

beta sugars have their anomeric hydroxyl group cis to the terminal carbon group.
alpha sugars have their anomeric hydroxyl group on the opposite side of the ring of the terminal carbon group. further, alpha is down in the chair position. fishes in the sea

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15
Q

triacylglycerol structure

A

glycerol molecule esterified to three fatty acid groups

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16
Q

lipase

A

enzyme that hydrolyzes fat

17
Q

cholesterol’s effects on phospholipid membrane fluidity

A

stabilizing; keeps membrane fluidity at an optimum level

18
Q

terpene

A

molecule built from isoprenes
isoprene general formula: (C5H8)
terpenes are mutliples of the isoprene molecular formula

19
Q

steroid structure

A

polycyclic amphipath derived from cholesterol. generally tetracyclic

20
Q

linkage holding multiple phosphates together in ATP

A

anhydride

21
Q

reasons for ATP high energy

A

three phosphate groups have a great deal of negative charge in close proximity.

orthophosphate has a better resonance

orthophosphate interacts with water better than linked phosphates