Knowledge blocks Flashcards

1
Q

Tyrpsin

A

Cut right of LYS and ARG

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2
Q

Chymotyrpsin

A

cut to the right of aormatic amino acids such as PHE, TRY and TRP

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3
Q

Elastase

A

Cut to the right of the three smallest amino acids GLY, ALA, SER

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4
Q

CNBr

A

Cut to the right of MET

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5
Q

Aminopeptidase

A

Curt to the right of the amino terminal of amino acid

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6
Q

Mercaptoethanol

A

breaks up disulfide bonds

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7
Q

4 effects of ACIDOSIS

A

GABA increase Denatures protein Hyperkalemia leads to arrhythmias Kussmaul breathing

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8
Q

Organ with the lowest km for any substrate = highest affinity or potency

A

Brain

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9
Q

5 pathways occur in both compartment

A

Heme synthesis Gluconeogenesis Urea cycle Fatty acid synthesis Pyrimidine synthesis

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10
Q

Energy Utilization

A

Plasma (serum) glucose = lasts 2 - 4 hours Liver glycogen = lasts 24- 48 Proteolysis for glconeogenesis = starts at 2 days Lipolysis = begins at end of day 2 ketogenesis

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11
Q

Opiates

A

CNS depressants

Muscle relaxants

Analgesics

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12
Q

Reducing agent

A

Negative delta E

Gives away electrons

Oxidized after reaction

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13
Q

Oxidizing agent

A

Positive delta E

Accepts electrons

Reducued after reaction

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14
Q

XR

A

G6PD

Fabry’s

Hunter’s

CGD

Adrenoleukodystrophy

ADA

OTC

PRPP synthetase

Tyrosine Kinase

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15
Q

Classes of Neurotransmitters

A

AA

monoamines

peptides

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16
Q

AA inhibitory neurotransmitters

A

GABA of the brain

Glycine of the spinal cord

17
Q

AA excitatory neurotransmitters

A

Glutamate

Aspartate

18
Q

Monoamines neurotransmitter

A

Dopamine

norepinephrine

epinephrine

serotonin

19
Q

Polypeptides

A

CCK

Substance P

Neurpeptide

others:

Opioids

endocannabinoids

NO/CO

20
Q

PEEP

A

Prevent atelectasis

↑ Oxygenation without increasing the risk of oxygen toxicity

↑ Gas exchange area

↑ Functional residual capacity

↑ Pulmonary compliance

21
Q

Which values are prevalence dependant

A

PPV and NPV

22
Q

AD (17)

A

Achondroplasia

Autosomal dominant polycystic kidney disease (ADPKD)

Ehler-Danlos syndrome

Familial adenomatous polyposis

Familial hypercholesterolemia

Hereditary spherocytosis

Huntington disease

Li-Fraumeni syndrome

Marfan syndrome

Multiple endocrine neoplasias

Myotonic muscular dystrophy

Neurofibromatosis type 1

Neurofibromatosis type 2

Osler-Weber-Rendu syndrome

Osteogenesis imperfecta

Tuberous sclerosis

Von Hippel-Lindau disease

23
Q

AR (13)

A

Oculocutaneous albinism

ARPKD

Cystic fibrosis

Friedreich ataxia

Glycogen storage diseases

Hemochromatosis

Kartagener syndrome

Mucopolysaccharidoses (except Hunter syndrome, which is an X-linked recessive disorder)

Phenylketonuria

Sickle cell anemia

Sphingolipidoses (except Fabry disease, which is an X-linked recessive disorder)

Thalassemias

Wilson disease

24
Q

XD (4)

A

Alport syndrome

Fragile X syndrome

Hypophosphatemic rickets

Rett syndrome

25
Q
A