TLS Online TPP Program

#Question id: 715


A protein is made up of 200 amino acids with alpha helix region containing 100 amino acid residues and 80 amino acids making antiparallel beta sheet and rest 20 amino acids in extended form. What will be the total length of this protein?

#Unit 1. Molecules and their Interaction Relevant to Biology
  1. 360

  2. 520         

  3. 400  

  4. 550

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TLS Online TPP Program

#Question id: 24498

#Unit 3. Fundamental Processes

SR proteins are involved in exon definition in which they interact with U1 and U2AF forming the commitment for

TLS Online TPP Program

#Question id: 24491

#Unit 3. Fundamental Processes

There are three type of Splicing signals 1. Major U2-type or GU-AG introns 2. Minor U12-type or AU-AC introns & 3. Minor U12-type with GU-AG introns (hybrid type), which of the following is responsible for the recognition of branch point sequence CCUUAACU

TLS Online TPP Program

#Question id: 24490

#Unit 3. Fundamental Processes

There are three type of Splicing signals 1. Major U2-type or GU-AG introns 2. Minor U12-type or AU-AC introns & 3. Minor U12-type with GU-AG introns (hybrid type), which of the following is responsible for the recognition of branch point sequence UACUAAC?

TLS Online TPP Program

#Question id: 24489

#Unit 3. Fundamental Processes

Two transesterification reactions takes place for 2 exon -1 intron configuration. Choose the correct  statement 
a. First transesterification is always caused by exon 1 -3’OH
b. second transesterification is catalysed variably either by external G or branch point while .
c. First transesterification is catalysed variably either by external G or branch point while 
d. second transesterification is always caused by exon 1 -3’OH.

TLS Online TPP Program

#Question id: 24464

#Unit 3. Fundamental Processes

rRNA are encoded by two type of RNA pol. RNA pol I and RNA pol III in which 5.8s rRNA is encodes by …………. While 5s rRNA encoded by ……

TLS Online TPP Program

#Question id: 4350

#Unit 3. Fundamental Processes

Portions of the DNA sequences of normal and mutant b-globin genes are shown. The most plausible explanation for why the indicated mutation (changing an A to a G) results in the disease b-thalassemia is that the mutation