Under ‘‘dark conditions,” the [(A4-glyceraldehyde-3-phosphate dehydrogenase) 2•(phosphoribulokinase)2•(CP12)4] is formed by CP12 called supramolecular complex.

TLS Online TPP Program

#Id: 6111

#Unit 3. Fundamental Processes

Genes whose products are involved in controlling the fidelity of DNA synthesis during either replication or repair may be identified by mutations that have a mutator phenotype called as mut system of repair or MMR

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#Id: 6112

#Unit 3. Fundamental Processes

Mismatch Repair removes errors that escape Proofreading

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#Id: 6113

#Unit 3. Fundamental Processes

In Escherichia coli, MutS scans the DNA, recognizing mismatches from the distortion they cause in the DNA backbone. 

MutS has an ATPase activity that is required for mismatch repair and recruits MutL, a second protein component of the repair system. MutL, in turn, activates MutH, an enzyme that causes an incision or nick on one strand near the site of the mismatch. Nicking is followed by the action of a specific helicase (UvrD) helicase unwinds the DNA, starting from the incision and moving in the direction of the site of the mismatch, and the filled in by DNA polymerase III

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#Id: 6114

#Unit 3. Fundamental Processes

MutH protein binds at hemimethylated daughter strands created by dam methylase

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#Id: 6115

#Unit 3. Fundamental Processes

TLS Online TPP Program

#Id: 6116

#Unit 3. Fundamental Processes

The main MutS homologs in most eukaryotes are MSH2 (MutS homolog), MSH3, and MSH6.