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agasfer [191]
4 years ago
11

Rhodopsins are light-sensitive molecules composed of a protein (opsin) and retinal (derivative of vitamin a). opsin is a membran

e protein with several alpha-helical segments that loop back and forth through the plasma membrane. there are two classes of rhodopsins. according to oded beje, one class has relatively slow dynamics (a photocycle of approximately 0.5 second) and is well suited for light detection. the second class has faster dynamics (a photocycle of approximately 0.02 seconds) and is well suited for chemiosmosis-pumping of protons or chloride ions across cell membranes. oded beje was the first, in september 2000, to report on a rhodopsin (proteorhodopsin) found in the domain bacteria. [source: o. beje et al., science 289 (2000): 1902.] proteorhodopsin consists of a single polypeptide chain. what is the highest level of structure found in this protein?
Biology
1 answer:
kobusy [5.1K]4 years ago
4 0
The highest level of structure find in this protein is TERTIARY.
There are four different structural levels of protein formation, these are the primary, secondary, tertiary and the Quaternary level.
The tertiary structural level of protein is usually formed by the folding of the secondary structures of the protein. The tertiary structure of a protein determines its functions.
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3 years ago
Whats the Location and the Structure for prestsynaptic membrane
Sergeeva-Olga [200]

Answer:

The presynaptic membrane is formed by the part of the presynaptic axon terminal forming the synapse and that of the postsynaptic neuron is called the postsynaptic membrane. The space between the presynaptic and postsynaptic membrane is called the synaptic cleft. These three structures together form the synapse.

Explanation:

5 0
3 years ago
Which hormone increases osteoclast activity to release more calcium ions into the bloodstream?
Nesterboy [21]

Answer: both parathyroid hormone and calcitrol.

Explanation:

In the body calcium homeostasis, which is generally defined as the maintenance of specific internal conditions, is mediated by the endocrine system through hormonal control; hormones are usually specialized signal molecules derived from lipids or amino acids. This regulates the calcium flux between the bloodstream and the bone; and the hormones responsible, change the ratio of osteoclast activity to osteoblast activity -osteoblasts build bone while osteoclasts breakdown or degrade bone.

Hormones responsible include calcitonin (from special parafollicular cells in the thyroid gland), cacitrol (activated vitamin D) and the parathyroid hormone (from the  parathyroid glands).  These affect the absorption of calcium from the gut, or kidney reabsorption; both parathyroid hormone and calcitrol act by causing the release of calcium ions into the bloodstream as the bone is degraded by osteoclasts.

4 0
3 years ago
Aquatic ecosystems support more primary producers proportional to their area than terrestrial ecosystems. true or false
Andru [333]
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8 0
3 years ago
Read 2 more answers
Imagine a genetic counselor working with a couple who have just had a child who is suffering from Tay-Sachs disease. Neither par
Alexxx [7]

Answer:

C. "Because you have had one child with Tay-Sachs, you must each carry the allele. Any child you have has a 25% chance of having the disease

Explanation:

Tay-Sachs disease is an autosomal recessive disorder that means a child will acquire the phenotype or we can say disease only when both the alleles which cause disease are present in the child.

Here, in this condition neither parent has Tay-Sachs but they gave birth to a child who is suffering from the disease then it simply means that both the parents are carrier of this disease i.e. they both are heterozygous.

The cross and probability of healthy and diseased child is shown as under:

                          Mother        Father

Parents                    Tt               Tt

                              /        |          |     \

Off-springs         TT      Tt       Tt      tt

<u>Out of these 4 probable off-springs only 3 with genotype TT, Tt & Tt  will be healthy while the 1 with genotype tt will be diseased.</u><u> </u><u>So, the probability of diseased child is 1/4 which is 25%. </u>

Also, the birth of children is an independent event so if one child has already been born with this disease then it doesn't mean that the next 3 children will be healthy for sure i.e. birth of first child cannot influence the next child. In short we can also say that in the next birth, there is still 25% chance of the child being born with this disease because previous birth has nothing to do with next birth.

7 0
3 years ago
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