Hemoglobin and Binding Flashcards

1
Q

How many alpha helices exist in myoglobin or a hemoglobin subunit?

A

8 (numbered A-H)

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2
Q

Where does the oxygen bind in hemoglobin?

A

In the heme group that resides between helices E and F.

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3
Q

What residue interacts to stabilize the iron bound in the heme group?

A

Histidine (proximal, F-helix)

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4
Q

What mutation causes sickle cell anemia?

A

Glu –> Val

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5
Q

Why hemoglobins coagulate in sickle cell patients?

A

Valine at position 6 of one of the subunits fits into a hydrophobic pocket on another protein causing it to stick. Coagulation is is worse in unoxygenated proteins

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6
Q

Membrane Anchors are often derivatives of…

A

Post translational modifications

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7
Q

Major contacts between the subunits of hemoglobin are located where?

A

a1b1, a2b2

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8
Q

Sliding contacts of hemoglobin are located where?

A

a1b2, a2b1

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9
Q

What are the sliding contacts?

A

19 amino acids that change significantly 6A during O2 binding

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10
Q

What happens on O2 binding?

A

15 degree rotation between the two alpha and beta dimers

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