Table 12.1.5.3

Carvin, D.; Islam, S. A.; Sternberg, M. J. E.; Blundell, T. L.

doi:10.1107/97809553602060000679

International
Tables for
Crystallography
Volume F
Crystallography of biological macromolecules
Edited by M. G. Rossmann and E. Arnold

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International Tables for Crystallography (2006). Vol. F. ch. 12.1, p. 251 | 1 | 2 |

Table 12.1.5.3

D. Carvin,^a S. A. Islam,^b M. J. E. Sternberg^b and T. L. Blundell^c ^*

^a Biomolecular Modelling Laboratory, Imperial Cancer Research Fund, 44 Lincoln's Inn Field, London WC2A 3PX, England,^bInstitute of Cancer Research, 44 Lincoln's Inn Fields, London WC2A 3PX, England, and ^cDepartment of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge, CB2 1GA, England
Correspondence e-mail: tom@cryst.bioc.cam.ac.uk

Table 12.1.5.3 | top | pdf |
The five most popular mercury derivatives

The first column gives the number of times the reagent has been used in the analyses included in the heavy-atom data bank.

No.	Compound
101	Mercury(II) acetate
98	Mercury(II) chloride
85	Ethylmercurythiosalicylate (EMTS)
82	Potassium tetraiodomercurate(II)
81	para -Chloromercuriobenzenesulfonate (PCMBS)