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 Results for DC.creator="M." AND DC.creator="J." AND DC.creator="E." AND DC.creator="Sternberg" in section 12.1.5 of volume F
Protein chemistry of heavy-atom reagents
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5, pp. 321-324 [ doi:10.1107/97809553602060000837 ]
... solvent (e.g. acetonitrile). Tetrakis(acetoxymercurio)methane (TAMM) and di-m-iodobis(ethylenediamine)diplatinum(II) nitrate (PIP) have better solubility in ... reviewed by Thygesen et al. (1996). References Abraham, D. J., Phillips, S. E. V. & Kennedy, P. E. (1983). Methylphenylmercury: a novel ...

Iodine
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5.6, p. 324 [ doi:10.1107/97809553602060000837 ]
Iodine 12.1.5.6. Iodine In addition to their use in isomorphous replacement, iodine derivatives of crystalline proteins have been prepared as tyrosine or histidine markers to assist main-chain tracing and to act as a probe for surface residues. The order of reactivity towards these reactive residues is , I-, I+ and I2 ...

Hydrophobic heavy-atom reagents
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5.5, pp. 323-324 [ doi:10.1107/97809553602060000837 ]
... has attractions for multiple-wavelength anomalous dispersion. References Abraham, D. J., Phillips, S. E. V. & Kennedy, P. E. (1983). Methylphenylmercury: a novel heavy atom reagent for ...

Electrostatic binding of heavy-atom anions
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5.4, p. 323 [ doi:10.1107/97809553602060000837 ]
Electrostatic binding of heavy-atom anions 12.1.5.4. Electrostatic binding of heavy-atom anions Positively charged groups of proteins, such as the [alpha]-amino terminus, -amino of lysine, guanidinium of arginine and imadazolium of histidine, may form ion pairs with heavy-atom anionic complexes. For example, and can bind through electrostatic interactions. ...

B-metal reagents
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5.3, pp. 321-323 [ doi:10.1107/97809553602060000837 ]
... crystals. References Petsko, G. A., Phillips, D. C., Williams, R. J. P. & Wilson, I. A. (1978). On the protein crystal ... chloroplatinite ions: general principles and interactions with triose phosphate isomerase. J. Mol. Biol. 120, 345-359. Sasaki, K., Dockerill, S., Adamiak, D. A., Tickle, I. J. & Blundell, T. L. (1975). X-ray analysis of ...

Thallium and lead ions
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5.2, p. 321 [ doi:10.1107/97809553602060000837 ]
Thallium and lead ions 12.1.5.2. Thallium and lead ions Thallium and lead can provide useful derivatives, especially in their lower oxidation states, Tl(I) and Pb(II), when they resemble class A metals. Owing to the non-group valence and presence of an inert pair of electrons, the ionic radii of ...

Hard cations
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5.1, p. 321 [ doi:10.1107/97809553602060000837 ]
Hard cations 12.1.5.1. Hard cations Uranyl-ion complexes have proved the most popular A-group metal reagents for preparing heavy-atom derivatives of protein crystals (see Table 12.1.5.1). is a linear, covalent group based on U(VI), the most stable oxidation state of uranium. Table 12.1.5.2 lists the most commonly ...

Polynuclear reagents
Carvin, D., Islam, S. A., Sternberg, M. J. E. and Blundell, T. L.  International Tables for Crystallography (2012). Vol. F, Section 12.1.5.7, p. 324 [ doi:10.1107/97809553602060000837 ]
... solvent (e.g. acetonitrile). Tetrakis(acetoxymercurio)methane (TAMM) and di-m-iodobis(ethylenediamine)diplatinum(II) nitrate (PIP) have better solubility in ... al. (1996). References O'Halloran, T. V., Lippard, S. J., Richmond, T. J. & Klug, A. (1987). Multiple heavy-atom reagents for ...

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