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Domains & Domain Classification

gina_evans0312 37 preguntas

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Preguntas del test (37)

  1. 1Of known structures (60-80% of genes) how many are multidomain proteins?
    1. A40
    2. B50
    3. C60
    4. D30
  2. 2Different combinations of domains are advantageous because they allow the organism to specialise
    1. AVerdadero
    2. BFalso
  3. 3How can we recognize domains?
    1. ADNA sequencing
    2. BAmino acid sequencing
    3. CStructure
    4. DTopology (fold)
  4. 4Why are DNA/amino acid sequencing of little use when investigating relationships between proteins?
    1. AAs diversion occurs, sequence patterns are lost even as the fold remains the same
    2. BThey can detect short evolutionary relationships only
    3. CThe techniques for reading the sequences are unreliable
    4. DIdentical sequences can give different aa sequences/folds
  5. 5When investigating using structure, how do we identify domains?
    1. AAmino acid sequence
    2. BDomains have the same fold
    3. CThe interaction of the protein with other proteins
  6. 6There is a limited number of folds in nature (10^3-4)
    1. AVerdadero
    2. BFalso
  7. 7Structural similarity occurs from what kind of evolution?
    1. ADivergent
    2. BConvergent
  8. 8Sequence is more highly conserved than protein structure
    1. AVerdadero
    2. BFalso
  9. 9Define convergent evolution
    1. AThe independent evolution of similar features in different lineages
    2. BThe carrying of a feature from a common ancestor into two lines, which allows the reconvergence of the two lines into a single species again
    3. CThe dependent evolution of similar features in two species that interact/co-operate closely
  10. 10How does the CATH system establish taxonomy?
    1. ACut proteins into domains and use computor analysis to group domains
    2. BUses structure based analysis

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Descripción
(Basics) Structural Basis for Biological Function Test sobre Domains & Domain Classification, creado por gina_evans0312 el 13/12/2013.
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