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Directional Aspects of Intermolecular Interactions 53 gen phosphorylase b [107] and the blue-light photoreceptor photoactive yellow protein [108]. 11 Conclusion We are now learning much about intermolecular interactions and reactions from the types of studies described here. An understanding of directional preferences of binding of functional groups is an essential starting point for proposals on mechanisms of reactions between two molecules, large or small, and also for the construction of supramolecular assemblies, be they in solution or in the solid state, the latter being in the focus of interest here. Acknowledgment. This work was supported by grants CA-10925 and CA-06927 from the National Institutes of Health, and by an appropriation from the Commonwealth of Pennsylvania. The contents of this article are solely the responsibility of the authors and do not necessarily represent the official views of the National Cancer Institute. 12 References 1. Legon AC, Millen DJ (1993) Molecular recognition involving small gas-phase molecules. In: Buckingham AD, Legon AC, Roberts SM (eds) Principles of molecular recognition. Blackie, London, p17 2. Buckingham AD (1993) Intermolecular forces. In: Buckingham AD, Legon AC, Roberts SM (eds) Principles of molecular recognition. Blackie, London, p1 3. Jeffrey GA (1997) An introduction to hydrogen bonding. Oxford University Press, New York 4. Allen FH, Bellard S, Brice MD, Cartwright BA, Doubleday A, Higgs H, Hummelink T, Hummelink-Peters BG, Kennard O, Motherwell WDS, Rodgers JR,Watson DG (1979) Acta Cryst B35:2331 5. Bernstein FC, Koetzle TF, Williams GJB, Meyer EF Jr, Brice MD, Rodgers JR, Kennard O, Shimanouchi T, Tasumi M (1977) J Mol Biol 112:535 6. Berman HM, Olson WK, Beveridge DL, Westbrook J, Gelbin A, Demeny T, Hsieh S-H, Srinivasan AR, Schneider B (1992) Biophys J 63:751 7. Bergerhoff G, Hundt R, Sievers R, Brown ID (1983) J Chem Info 23:66 8. Matthews BW (1968) J Mol Biol 33:491 9. Murray-Rust P, Glusker JP (1984) J Am Chem Soc 106:1018 10. Rosenfield RE Jr, Swanson SM, Meyer EF Jr, Carrell HL, Murray-Rust P (1984) J Mol Graphics 2:43 11. Williams DE (1972) Acta Cryst A 28:629 12. Kitaigorodsky AI (1955) Organic chemical crystallography. Consultants Bureau, New York 13. Gavezzotti A (1994) Acc Chem Res 27:309 14. Glusker JP, Carrell HL, Berman HM, Gallen B, Peck RM (1977) J Amer Chem Soc 99:595 15. Vedani A, Dunitz JD (1985) J Am Chem Soc 107:7653 16. Vedani A, Huhta DW (1990) J Am Chem. Soc 112:4759 17. Klebe G (1994) J Mol Biol 237:212 18. Rosenfield RE Jr, Parthasarathy R, Dunitz JD (1977) J Am Chem Soc 99:4860 19. Fukui K, Yonezawa, T, Shingu H (1952) J Chem Phys 20:722 20. Guru Row T, Parthasarathy R (1981) J Am Chem Soc 103:477 21. Chakrabarti P (1989) Biochem 28:6081 22. Ramasubbu N, Parthasarathy R, Murray-Rust P (1983) J Am Chem Soc 105:3206
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198 Topics in Current Chemistry Edi
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Design of Organic Solids Volume Edi
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Volume Editors Prof. Dr. Edwin Webe
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VIII preface tion at an amazing lev
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Contents of Volume 196 Carbon Rich
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Springer and the environment At Spr
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