Similarly NMR (nuclear magnetic resonance) technique will allow us to know the structure of enzymes in solution rather than in crystals, so that we can bypass the time consuming process of crytallization thus speeding up the study of protein structure. The information generated from all these techniques is utilized in protein modelling, which is then utilized for an exercise in protein engineering.
When crystals of a protein are not available for study, but amino acid sequence data is available, the identical sequences in any two proteins are matched and effects of substitution are examined. This is simetimes described as 'sequence garing' and allows us to know which amino acids are involved in catalytic binding at active sites.
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