TLS Online TPP Program

#Question id: 696


An alpha helix would be destabilized most by:

#Unit 1. Molecules and their Interaction Relevant to Biology
  1. an electric dipole spanning several peptide bonds throughout the Alpha helix.

  2. interactions between neighboring Asp and Arg residues.

  3. interactions between two adjacent hydrophobic Val residues.

  4. the presence of two Lys residues near the amino terminus of the alpha helix.

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TLS Online TPP Program

#Question id: 5322

#Unit 11. Evolution and Behavior

A current view of how the human and chimpanzee can share most of their nucleotide sequences yet exhibit significant phenotypic differences is that many of the most important sequence differences alter ________.

TLS Online TPP Program

#Question id: 5323

#Unit 8. Inheritance Biology

An X-linked recessive gene produces red-green color blindness in humans. A woman with normal color vision whose father was color-blind marries a color-blind man. What is the probability that their son will be color-blind?

TLS Online TPP Program

#Question id: 5324

#Unit 8. Inheritance Biology

In eusocial insects, males develop from unfertilized eggs while females develop from fertilized eggs. The ultimate consequence of this difference is that

TLS Online TPP Program

#Question id: 5325

#Unit 8. Inheritance Biology

Cystic fibrosis is caused by a recessive lethal gene and can be detected by an excess concentration of chloride in sweat. A normal man whose sister has cystic fibrosis, his normal wife whose brother has cystic fibrosis. What is chance of cystic fibrosis in their child?

TLS Online TPP Program

#Question id: 5326

#Unit 8. Inheritance Biology

The recessive allele located on heterozygous locus present on X-chromosome in female is conclude as

TLS Online TPP Program

#Question id: 5327

#Unit 8. Inheritance Biology

In the human pedigree shown here, the daughter indicated by the black circle (II-1) has a form of deafness determined by a recessive allele. What is the probability that the phenotypically normal son (II 3) is heterozygous for the gene?