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Introduction to Protein Science Architecture, Function, and Genomics Arthur M. Lesk Chapter 2: Genomics and Proteomics P47-51 2008-11-10 Jeong, Da-Geum, UST Chapter2: Genomics and Proteomics - Protein evolution Flow of Change----------------------------- 2.Amino acid or 1.Nucleic acid expression pattern of protein Selected advantage 3.Activity of the Protein Disadvantage Exception: Silent mutation Ex: 3rd position in exons, untranslated regions Simplest change to a protein is the substitution of a single amino acid Then, what is the effect on the protein structure and function? Chapter2: Genomics and Proteomics - Protein evolution 2. Change of the Structure(folding) 1.No noticeable effect Ex) Hemoglobin b-chain mutation -> Robust protein to mutation B60Val-> Glu, - rapid degraded Ex) enzymes in closely related species B106Leu->Arg - precipitate Substitution of (a single) amino acid 3.Sensitive position in the active site Ex) Gln-> Arg substitution, Malate dehydrogenase -> 4. Easy to aggregate-> Very serious clinical consequence Ex) Sickle cell anaemia, Z-mutant of a1-antitrypsin Lactate dehydrogenase Other type of change 1 Insertion 2 Deletion – cystic fibrosis 3 Transpositions – degraded in the ER Chapter2: Genomics and Proteomics - Protein evolution How do proteins develop new functions? (1) Divergence – progressive localized changes in sequence and structure -> initially to change in specificity -> ultimately to changes in the nature of the reaction catalysed (2) Recruitment – one protein is adapted (3)‘Mixing and matching’ of domains or modular evolution - large-scale structural changes - Individual domain-> gain of function, modified function, different processes. Robustness of protein structure to mutations is a maintenance of structure in spite of the divergence of sequences during evolution