IR WEEK 4 Flashcards

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1
Q

are bound via noncovalent interactive with other membrane proteins

A

Peripheral membrane proteins

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2
Q

held in the hydrophobic core of the lipid bilayer and cannot be released easily

A

transmembrane proteins

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3
Q

illustrate the number of amino acids of a transmembrane protein located within a cell membranes lipid bilayer (~20-30); also how many membrane spanning domains there are

A

hydropathy plots

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4
Q

spectrin mutation, produces RBCs that have unusual cell membrane properties… inflexible, destroyed quickly leads to anemia

A

hereditary spherocytosis

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5
Q

measures the rate at which the carrier can flip its conformation. it is specific for each transport protein and is reflected by km

A

vMAX

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6
Q

transport of one solute to transport of another

A

coupled transport

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7
Q

co transporters that involve simultaneous transfer of a second solute in the same direction of the first solute

A

symporters

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8
Q

list the two types of coupled transport

A

symport and antiport

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9
Q

exchangers that move one substance in and another out; function is to maintain cellular pH

A

antiporters

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10
Q

most diseases are the result of cell communication breakdown: signals are lost

A

diabetes type 1
loss of immune protection

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11
Q

most diseases are the result of cell communication breakdown: cell signals do not reach target

A

multiple sclerosis

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12
Q

most diseases are the result of cell communication breakdown; target cell does not respond

A

diabetes type 2

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13
Q

most diseases are the result of cell communication breakdown; too much signal

A

stroke with release of glutamate in the brain

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14
Q

a motor protein that slides along actin polymers for muscle contraction using ATP hydrolysis

A

myosin

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15
Q

growth to shrinkage

A

catastrophe

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16
Q

shrinkage to growth

A

rescue

17
Q

paralyzed cilia so chronic lung disease due to sufficient movement of cilia from defect in dynein arms; mutations on two genes DNAI1 and DNAH5 on chromosome 9, both of which encode for proteins found in the ciliary outer dynein arm lead to this syndrome

A

kartagener syndrome

18
Q

genetic defect in keratins; skin ruptures or blisters with any mechanical stress

A

epidermyolysis bullosa

19
Q

contact with an adhesion protein in the substrate

A

contact-mediated attraction/ repulsion

20
Q

attraction to an emitted chemical cue

A

chemoattraction/chemorepulsion

21
Q

neural tube closure requires numerous cellular events based on cell migration

A

spina bifida

22
Q

sertoli cells have altered cytoskeleton and lack androgen receptors on nucleus; alterations in these cells cytoskeleton during development produce infertility

A

kennedy disease

23
Q

protein enzymes that add phosphates to various proteins involved in cell cycling

A

cyclin dependent kinases

24
Q

a ubiquitin ligase that catalyzes the destruction of major proteins; securin (protects protein links between sister chromatids and unleashes anaphase) and S- and M-cyclins

A

APC/C

25
Q

cyclin D

A

G1 Cyclin

26
Q

Cyclin E

A

G1/S Cyclin

27
Q

Cyclin A

A

S cyclin

28
Q

Cyclin B

A

M Cyclin

29
Q

a ubiquitin ligase that catalyzes the destruction of major proteinsn

A

Cyclosome APC/C

30
Q

microtubule organizing center that has centrioles and nucleation sites; important during mitosis

A

centrosome.