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Trends and Challenges in Experimental Macromolecular Crystallography

Authors :
Chayen, N. E.
Boggon, T. J.
Cassetta, A.
Deacon, A.
Gleichmann, T.
Habash, J.
Harrop, S. J.
Helliwell, J. R.
Nieh, Y. P.
Peterson, M. R.
Raftery, J.
Snell, E. H.
Hädener, A.
Niemann, A. C.
Siddons, D. P.
Stojanoff, V.
Thompson, A. W.
Ursby, T.
Wulff, M.
Chayen, N. E.
Boggon, T. J.
Cassetta, A.
Deacon, A.
Gleichmann, T.
Habash, J.
Harrop, S. J.
Helliwell, J. R.
Nieh, Y. P.
Peterson, M. R.
Raftery, J.
Snell, E. H.
Hädener, A.
Niemann, A. C.
Siddons, D. P.
Stojanoff, V.
Thompson, A. W.
Ursby, T.
Wulff, M.
Publication Year :
2017

Abstract

Macromolecular X-ray crystallography underpins the vigorous field of structural molecular biology having yielded many protein, nucleic acid and virus structures in fine detail. The understanding of the recognition by these macromolecules, as receptors, of their cognate ligands involves the detailed study of the structural chemistry of their molecular interactions. Also these structural details underpin the rational design of novel inhibitors in modern drug discovery in the pharmaceutical industry. Moreover, from such structures the functional details can be inferred, such as the biological chemistry of enzyme reactivity. There is then a vast number and range of types of biological macromolecules that potentially could be studied. The completion of the protein primary sequencing of the yeast genome, and the human genome sequencing project comprising some 105 proteins that is underway, raises expectations for equivalent three dimensional structural databases

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1156695962
Document Type :
Electronic Resource