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63 Cards in this Set
- Front
- Back
thiamine pyrophosphate (TPP) is a co-factor for (3)
enzyme function |
transketolase (ribulose-5-phosphate --> fructose-6-phosphate)
pyruvate dehydrogenase (pyruvate --> acetyl-CoA) α-ketoglutarate dehydrogenase (α-ketoglutarate --> succinyl-CoA) note: pyruvate dehydrogenase and α-ketoglutarate dehydrogenase use the same co-factors (the first 4 water-soluble vitamins and lipoic acid) |
|
signs of riboflavin (vit. B2) deficiency (3)
|
cheilosis (scaling of lips/fissures at corners of lips)
corneal vascularization angular stomatitis |
|
niacin (vit. B3):
synthesized from co-factor needed for synthesis |
tryptophan
pyridoxine (vit. B6) |
|
causes of niacin (vit. B3) deficiency (3)
|
Hartnup disease (↓ tryptophan absorption)
malignant carcinoid syndrome (↑ tryptophan breakdown) INH (↓ pyridoxine) |
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pantothenate (vit. B5):
component of (2) |
acetyl-CoA
fatty acid synthase |
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pyridoxine (vit. B6) deficiency caused by (2)
|
INH
oral contraceptives |
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pyridoxal phosphate is a co-factor for (3)
|
transaminations (AST & ALT)
decarboxylations heme synthesis |
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cobalamin (vit. B12) is a co-factor for (2)
|
-homocysteine methylation (homocysteine methyl-transferase)
(homocysteine + N-methyl THF --> methionine + THF) -methylmalonyl-CoA handling (methylmalonyl-CoA --> succinyl-CoA) |
|
biotin is a co-factor for
examples (3) |
carboxylations:
pyruvate carboxylase (pyruvate --> oxaloacetate) - for gluconeogenesis acetyl-CoA --> malonyl-CoA (for FA synthesis) propionyl-CoA --> methylmalonyl-CoA (for TCA cycle) |
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vitamin C is a co-factor for (2)
|
NE synthesis
(DA --> NE) 5-HT synthesis (tryptophan --> 5-HT) |
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delayed wound healing, hypogonadism, and decreased adult hair results from
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zinc deficiency
|
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NADH/NAD+ ratio in alcoholism
effects (2) |
↑ NADH/NAD+
pyruvate --> lactate oxaloacetate --> malate (gluconeogenesis is inhibited) |
|
amino acids needed for purine synthesis
|
glycine
aspartate glutamine |
|
DNA replication in eukaryotes begins at
composition |
consensus sequence
AT-rich base pairs |
|
largest type of RNA
|
mRNA
|
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most abundant type of RNA
|
rRNA
|
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RNA polymerase II inhibited by
|
α-amanitin
|
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features of promoter sequence (2)
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TATA box
CAAT box |
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function of promoter
location |
start of transcription
upstream |
|
function of enhancer
location |
binding of TF's (increase transcription)
almost anywhere (upstream, downstream, within an intron) |
|
promoter mutation results in
|
↓ transcription
|
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spliceosome composed of (2)
|
primary transcript (introns + exons = hnRNA) and snRNP's
|
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permanent cells (3)
|
skeletal muscle
cardiac muscle RBC's |
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stable cells (2)
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hepatocytes
lymphocytes (induced to leave Go in the case of injury or infection) |
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labile cells (4)
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bone marrow
gut epithelium skin hair follicles |
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secretory (exported) proteins synthesized by
high levels found in (2) |
RER
goblet cells (secrete mucous) plasma cells (secrete Ab's) |
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N-linked oligosaccharide addition occurs in the
|
RER
|
|
modification of N-linked oligosaccharides occurs in the
modification occurs on |
Golgi
asparagine |
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O-oligosaccharide addition occurs in the
addition occurs on (2) |
Golgi
serine threonine |
|
addition of mannose-6-phophate occurs in the
result |
Golgi
protein targeted to lysosome |
|
sulfation of sugars in proteoglycans occurs in the
|
Golgi
|
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proteoglycan assembly occurs in the
|
Golgi
|
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coarse facial features, clouded corneas, restricted joint movement, and high plasma levels of lysosomal enzymes is characteristic of
|
I-cell disease
|
|
Chediak-Higashi syndrome
defect result |
microtubule polymerization defect
↓ phagocytosis (decreased mobility of phagocytes) |
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phosphatidylcholine found in (4)
|
RBC membranes
myelin bile surfactant |
|
phosphatidylcholine is used in the
|
esterifcation of cholesterol by LCAT
|
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cartilage type:
bones |
I
|
|
cartilage types:
skin |
I and III (reticulin)
|
|
cartilage type:
tendons |
I
|
|
cartilage type:
dentin |
I
|
|
cartilage type:
fascia |
I
|
|
cartilage type:
cornea |
I
|
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cartilage type:
late wound repair |
I
|
|
cartilage type:
cartilage (including hyaline) |
II
|
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cartilage type:
vitreous body |
II
|
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cartilage type:
nucleus pulposus |
II
|
|
cartilage type:
blood vessels |
III (reticulin)
|
|
cartilage type:
uterus |
III (reticulin)
|
|
cartilage type:
fetal tissue |
III (reticulin)
|
|
cartilage type:
granulation tissue |
III (reticulin)
|
|
steps of collagen synthesis within fibroblasts
location |
synthesis (RER)
hydroxlation (ER) glycosylation (Golgi) exocytosis |
|
steps of collagen synthesis outside fibroblasts
|
proteolytic processing
cross-linking |
|
function of lysyl oxidase
|
covalently cross links lysine-hydroxylsine
|
|
Ehlers Danlos syndrome
due to results in |
faulty collagen synthesis (most commonly type III)
blood vessel instability --> berry aneurysm |
|
Osteogenesis Imperfecta
due to MOI signs (4) |
abnormal collagen synthesis (most commonly type I)
AD multiple fractures blue sclerae hearing loss dental imperfections |
|
vimentin stains
|
CT
|
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desmin stains
|
muscle
|
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elastin found within (3)
|
lungs
large arteries elastic ligaments |
|
elastin is rich in (2)
|
nonhydroxylated proline and lysine
|
|
site of:
fatty acid synthesis |
cytoplasm
|
|
site of:
gluconeogenesis |
mitochondria (oxaloacetate) and cytoplasm
|
|
site of:
urea cycle |
mitochondria (citriline) and cytoplasm
|
|
site of:
heme synthesis |
mitochondria and cytoplasm
|