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54 Cards in this Set

  • Front
  • Back
carbamoyl phosphate is used in...
urea cycle

de novo pyrimidine synthesis
difference between purine & pyrimidine synthesis
purines: built on a PRPP "scaffold"

pyrimidines: orotic acid (~ a base) is built, then PRPP is added to it
5 drugs that interfere with nucleotide synthesis, and what they inhibit
hydroxyurea: - ribonucleotide reductase
6-mercaptopurine: purine analog; - de novo purine synthesis
5-fluorouracil: - thymidylate synthase
methotrexate: - dihydrofolate reductase
trimethoprim: - dihydrofolate reductase
aa's used in purine synthesis
glycine
aspartate
glutamine
components of pyrimidine synthesis
carbamoyl phosphate
aspartate
two bases have two interesting functional groups
guanine: ketone
THYmine: meTHYl
deamination of _ --> _
cytosine-->uracil
3 ways euchromatin differs from chromatin
less condensed
transcriptionally active
sterically accessible
orotic aciduria may be caused by...
1. defective orotic acid phosphoribosyltransferase

3. defective orotidine 5'-phosphate decarboxylase

(1) and (2) --> inability to convert orotic acid to UMP
orotic aciduria may be caused by 2 enzyme defects
orotic acid phosphoribosyltransferase

orotidine 5'-phosphate decarboxylase
findings of orotic aciduria
^ orotic acid in urine

megaloblastic anemia (does not improve with B12 or folate)

failure to thrive
OTC deficiency
ornithine transcarbamoylase deficiency
--> accumulation of carbamoyl phosphate
--> ^ orotic acid
orotic aciduria vs.

OTC deficiency
^ orotic acid, no hyperammonemia

^ orotic acid with hyperammonemia
treatment for orotic aciduria
oral uridine
Lesch-Nyhan syndrome mecahnism (3)
defective purine salvage

2^ HGPRT absence

--> excess uric acid production
Lesch-Nyhan syndrome symptoms (6)
his ARS has hCG written on it

aggression
retardation
self-mutilation

hyperuricemia
choreoathetosis
gout
methionine: what codon?
AUG
example organisms that have exceptions to the universal genetic code
mitochondria, archaebacteria, mycoplasma, some yeasts
primase does...
makes an RNA primer

on which DNA polymerase III can initiate replication
DNA polymerase I does...
degrades RNA primer

fills in the gap with DNA
DNA polymerase III directions in which it works
synthesis: 5' --> 3'

exonuclease (proofreading):
3'-->5'
two prokaryotic DNA polymerases
DNA pol III
DNA pol I
exonuclease in DNA pol III and DNA pol I
pol III: 3'-->5'

pol I: 5'-->3'
4 types of DNA repair
nucleotide excision repair
base excision repair
mismatch repair

double strand nonhomologous end joining
_ DNA repair is mutated in _

(2)
nucleotide excision repair: xeroderma pigmentosum

mismatch repair: HNPCC
nucleotide excision repair vs.

base excision repair enzymes
endonucleases vs.

--glycosylases
--AP endonuclease (cuts at AP site)
---------------------------------
(DNA polymerase
DNA ligase)
mismatch repair is...
recognition of mismatched bases

in the newly synthesized strand (which is recognized e.g. in proks because it's unmethylated)
xeroderma pigmentosum sxs and a molecular defect
dry skin
melanoma
other cancers

thymidine dimers
DNA & RNA are synthesized from

_' to _'. what is the energy source?
5' to 3'

5' triphosphate of the incoming nucleotide
mRNA is read from _ to _; protein synthesis is from _ to _
5' to 3'

N to C
start codon
AUG; rarely GUG
the promoter is bound by...

describe the promoter
RNA polymerase
transcription factors

AT-rich
CAAT and TATA boxes
_ binds transcription factors, but _ binds _
enhancer

silencer binds repressors aka negative regulators
euks vs. proks:

RNA polymerase
euks: RNA polymerase I makes rRNA

II: mRNA
III: tRNA

proks: there's one RNA polymerase
_ opens DNA at promoter site
RNA pol II
RNA polymerase lacks _ ability but has _ ability
proofreading

can initiate without a primer
_ is found in death cap mushrooms
alpha-amanitin
alpha-amanitin (3)
found in death cap mushrooms

inhibits RNA pol II

causes liver failure
5' cap =
7-methylguanosine
polyadenylation signal =
AAUAAA
_ disease makes antibodies to spliceosomal snRNPs
lupus
intron hnRNA goes where?
stays IN the nucleus
_ disease is notable for having mutations affecting splicing of its hnRNA
beta-thalassemia
mechanism of tetracyclines
bind 30S subunit

prevent attachment of
aminoacyl-tRNA
there are _ aminoacyl-tRNA synthetases per aa
1 per aa
where does energy for peptide bond come from?
aa-tRNA bond
wobble is all about the 3rd position in the _
mRNA's codon
initiation of protein synthesis involves 5 things
GTP hydrolysis
eIFs that help assemble the
40S subunit with the
initiator tRNA

... then the eIFs are released
protein synthesis:

stop codon is recognized by
release factor
aminoglycosides MOA
inhibit formation of the initiation complex

--> misreading of mRNA
chloramphenicol MOA
inhibits 50S peptidyltransferase
macrolides and clindamycin MOA
bind 50S and block translocation
posttranslational modifications include
trimming

covalent alterations

proteasomal degradation