The answer is pulmonary
artery. This is an artery in the circulation that holds the deoxygenated blood from the heart to the lungs<span>. The biggest
pulmonary artery is the pulmonary trunk from the heart and the smallest are
found next to the pulmonary alveoli<span>.</span></span>
Answer:
provides energy and insulation
Explanation:
the biomolecule is carbohydrates or lipids
The answer is; SET B
Polar molecules interact well with water because there are charged. Water molecules are partially charged (the oxygen end is partially negative while the hydrogen end is partially positive). Therefore polar molecules can interact stably with charged molecules. The hydrophobic end is non-polar and is ‘water-hating’. When mixed with water, the non-polar region clumps up into globules so they don’t interact with water.
The question is incomplete. The complete question is as follows:
Which of the following mutations is most likely to cause a phenotypic change?
A) a duplication of all or most introns
B) a large inversion whose ends are each in intergenic regions
C) a nucleotide substitution in an exon coding for a transmembrane domain
D) a single nucleotide deletion in an exon coding for an active site
E) a frameshift mutation one codon away from the 3' end of the nontemplate strand
Answer: D) a single nucleotide deletion in an exon coding for an active site
Explanation:
Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.
The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.
Hence, the correct option is D) a single nucleotide deletion in an exon coding for an active site
.
