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Questions and Answers
What is the central metal ion in heme?
What is the central metal ion in heme?
How many pyrrole rings are there in a heme molecule?
How many pyrrole rings are there in a heme molecule?
Which of the following is NOT a hemoprotein?
Which of the following is NOT a hemoprotein?
How many heme groups are present in hemoglobin?
How many heme groups are present in hemoglobin?
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Which helix binds to the proximal histidine (F8) in hemoglobin?
Which helix binds to the proximal histidine (F8) in hemoglobin?
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What type of bond stabilizes the heme group in the globin pocket?
What type of bond stabilizes the heme group in the globin pocket?
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In hemoglobin, the sixth coordination site of iron binds to:
In hemoglobin, the sixth coordination site of iron binds to:
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What is one key role of the apoprotein part of hemoglobin?
What is one key role of the apoprotein part of hemoglobin?
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What is the Bohr effect in hemoglobin
What is the Bohr effect in hemoglobin
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why does hemoglobin have a higher affinity for CO than O2?
why does hemoglobin have a higher affinity for CO than O2?
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which amino acid in the polypeptide chain produces steric hindrance that produces CO binding affinity?
which amino acid in the polypeptide chain produces steric hindrance that produces CO binding affinity?
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What is the main function of myoglobin?
What is the main function of myoglobin?
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how many oxygen molecules can one hemoglobin molecule carry
how many oxygen molecules can one hemoglobin molecule carry
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which has a higher affinity for oxygen, myoglobin or hemoglobin
which has a higher affinity for oxygen, myoglobin or hemoglobin
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What percentage of adult hemoglobin is HbA?
What percentage of adult hemoglobin is HbA?
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Where is hemoglobin primarily located?
Where is hemoglobin primarily located?
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What is the structure of adult hemoglobin?
What is the structure of adult hemoglobin?
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and hemoglobin oxygen binding is facilitated by which structural property?
and hemoglobin oxygen binding is facilitated by which structural property?
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What type of protein structure does HbA1 have?
What type of protein structure does HbA1 have?
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How many alpha chains are present in HbA1?
How many alpha chains are present in HbA1?
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The two dims and hemoglobin are held together by
The two dims and hemoglobin are held together by
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which of the following describes the quaternary structure of hemoglobin?
which of the following describes the quaternary structure of hemoglobin?
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which of the following describes the quaternary structure of hemoglobin?
which of the following describes the quaternary structure of hemoglobin?
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what happens to the hemoglobin molecule when it binds to oxygen?
what happens to the hemoglobin molecule when it binds to oxygen?
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Which factor does not affect the oxygen binding ability of hemoglobin
Which factor does not affect the oxygen binding ability of hemoglobin
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Which of the following stabilizes the T form of hemoglobin
Which of the following stabilizes the T form of hemoglobin
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what is the role of 2,3- BPG in hemoglobin function?
what is the role of 2,3- BPG in hemoglobin function?
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Hemoglobin exhibits cooperative binding, this means:
Hemoglobin exhibits cooperative binding, this means:
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Hemoglobin exhibits cooperative binding, this means:
Hemoglobin exhibits cooperative binding, this means:
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Which bonds are broken during the T to R transition in hemoglobin?
Which bonds are broken during the T to R transition in hemoglobin?
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What molecule forms when liberated hydrogen ions bind with bicarbonate in the blood
What molecule forms when liberated hydrogen ions bind with bicarbonate in the blood
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The Bohr effect facilitates the release of oxygen in tissues by
The Bohr effect facilitates the release of oxygen in tissues by
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The Bohr effect facilitates the release of oxygen in tissues by
The Bohr effect facilitates the release of oxygen in tissues by
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Carbaminohemoglobin is formed when CO2 binds to
Carbaminohemoglobin is formed when CO2 binds to
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Carbon monoxide bonds through hemoglobin at the same site as
Carbon monoxide bonds through hemoglobin at the same site as
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which form of hemoglobin is toxic and prevents oxygen release in tissues
which form of hemoglobin is toxic and prevents oxygen release in tissues
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Which hemoglobin type is primarily present during the first three months of pregnancy?
Which hemoglobin type is primarily present during the first three months of pregnancy?
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Glycated hemoglobin (HbA1c) reflects blood glucose levels over the past:
Glycated hemoglobin (HbA1c) reflects blood glucose levels over the past:
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A HbA1c level greater than 6.5% typically indicates
A HbA1c level greater than 6.5% typically indicates
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Where is myoglobin primarily found?
Where is myoglobin primarily found?
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The alpha globin gene family is located on chromosome
The alpha globin gene family is located on chromosome
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Which gene is expressed during the first three months of pregnancy
Which gene is expressed during the first three months of pregnancy
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Hb Gower is formed by the combination of which chains?
Hb Gower is formed by the combination of which chains?
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Sickle cell anemia is caused by a mutation in the gene coding for
Sickle cell anemia is caused by a mutation in the gene coding for
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In sickle cell anemia, which amino acid is replaced in the beta globin chain?
In sickle cell anemia, which amino acid is replaced in the beta globin chain?
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Individuals with sickle cell treat have
Individuals with sickle cell treat have
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What amino acid is replaced by lysine in hemoglobin C (HbC) disease?
What amino acid is replaced by lysine in hemoglobin C (HbC) disease?
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What is a key symptom of hemoglobin C (HbC) disease?
What is a key symptom of hemoglobin C (HbC) disease?
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What happens in methemoglobinemia?
What happens in methemoglobinemia?
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What type of thalassemia results in the formation of Hb Bart (y4) and Hb H (beta 4)?
What type of thalassemia results in the formation of Hb Bart (y4) and Hb H (beta 4)?
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Which gene defect leads to alpha thalassemia major
Which gene defect leads to alpha thalassemia major
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Why does a patient with beta thalassemia major appear normal at birth?
Why does a patient with beta thalassemia major appear normal at birth?
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What is HbA2 composed of?
What is HbA2 composed of?
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What is the common characteristic of thalassemia disorders?
What is the common characteristic of thalassemia disorders?
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Which abnormal hemoglobin results from the replacement of histidine by tyrosine?
Which abnormal hemoglobin results from the replacement of histidine by tyrosine?
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