Videos- Biology Flashcards

(44 cards)

1
Q

Start codons

A

AUG

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2
Q

Stop codons

A

UAG, UAA, UGA

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3
Q

Pi/isoelectric point

A

the pH in which the aa is in it’s zwitterion (has no charge overall)

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4
Q

Wobble

A

3rd position doesn’t hav eto be a perfect match

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5
Q

exonuclease

A

chew from the outside

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6
Q

pKa values for an acidic amino acid uses…

A

the lowest 2 pKa values

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7
Q

pKa for a basic amino acid uses…

A

the 2 highest pKa values

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8
Q

endonuclease

A

cuts within the strand (like restriction enzymes)

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9
Q

Eukaryotic ribosome subunits

A

40s

60s

80s

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10
Q

Prokaryotic subunits

A

30S

50S

70S

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11
Q

___need 1 to reproduce while ___ need 2 cells

A

Prokaryotes need 1; eukaryotes need 2

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12
Q

A site

A

aminoacyl tRNA to load chain; new tRNA comes in

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13
Q

P site

A

Peptidyl tRNA holding the growing chain

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14
Q

primary structure

A

amino acid sequence

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15
Q

secondary structure

A

alpha helices and beta sheets; short range interactions

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16
Q

tertiary structure

A

long range interactions; disulfide bonds, salt bridges, hydrophobic interactions; myoglobin

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17
Q

quaternary structure

A

multiple subunits; hemoglobin

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18
Q

chaperone proteins

A

help give the protein a chance in a local environment; effecting in getting the cell to refold

19
Q

Helicase

20
Q

Topoisomerase

A

Makes sure supercoiling doens’t happen

21
Q

Primase

A

makes RNA primer

22
Q

DNA polymerase

A

adds the nucleotides to synthesize the new DNA strand

23
Q

DNA ligase

A

used on the lagging strand to connec the Okazaki fragments together

24
Q

RNA primer

A

~11 nucleotides long; where the DNA polymerase starts ot create the new piece of DNA

25
Single-strand binding proteins
prevents the strands reannealing
26
Telomere
repetitive nucleotide sequence at hte end of a chromosome
27
Semiconservative DNA experimeent
Messelson stahl experiment- radioactive nucleotides and measured the weight from the Nitrogenous base isotope
28
Which enzyme can tell if there's a mistake?
DNA polymerase has a proofreading function
29
DNA damage and fix process
1) xray or UV leads to damaged DNA 2) endonuclease removes the damaged DNA 3) gap is closed by DNA polymerase and ligase
30
Trp operon
repressible (normally on, but can be turned off)
31
Lac operon
inducible (typically off but can be turned on)
32
regulator
codes for the gene for the repressor that can bind to teh operator
33
promoter
where the RNA polymerase connects to teh strand
34
operator
where the repressor can sit
35
In the lac operon, the structural gene is
β-lactamase
36
in normal circumstances, the structural gene is turned...
off
37
prokaryotic specific initiation and termination components
sigma factor, hairpin, Rho factor
38
sigma factor
25-35 bp upstream before the gene, allows the RNA to sit down
39
hairpin loop
RNA folds back in on itself on teh DNA so that hte polymerase can't go any farther
40
Rho factor
termiantion fo transcription; 72 nucleotides after hte reading frame, GC rich region (harder to seperate, more h bonds)
41
eukaryotic specific initiation and elongation
TATA box, helicase
42
RNA polymerase I
located in the nucleolus and synthesizes tRNA
43
RNA polymerase II
located in the nucleus and synthesizes hnRNA (pre-processed mRNA) and some small nuclear RNA (snRNA)
44
RNA polymerase III
located in the nucleus and synthesizes tRNA and some rRNA