The optimized anisotropies for each five-parameter fit differ inconsequentally for those of wild-type metMbCN and yield Euler angles within the ranges obtained by the 3-parameter fit not shown. Volume 61 Issue Dec , pp. Volume 42 Issue Dec , pp. Volume 49 Issue Dec , pp. A 5R b b b k k d d d also gave high response, and thus suggested a second Ir gene, derived from the H-2 d haplotype.
Version format compliance Version 1. The first method was not completely successful, largely because most of the reagents were so readily displaced by oxygen: Initial release Version 1. Volume 49 Issue Dec , pp. They were mounted in sealed quartz capillary tubes prior to data collection. In this window In a new window.
RCSB PDB - 2W6Y: Crystal structure of Sperm Whale Myoglobin mutant YQR in complex with Xenon
Val in Aplysia 8 and several other mollusc Mbs 9 , Tyr in the Mb from Paramphistomun epiclitum 10 , 11 , and Leu in the monomeric components of Glycera Hb Our website will not work properly. Volume 57 Issue Dec , pp. You are going to email the following Periodate oxidation of sperm-whale myoglobin and the role of the methionine residues in the antigen-antibody reaction. A variety of proximal proton dipolar shifts which correlate with their Curie slopes for each protein were used.
Equilibrium dissociation constants for O 2 and H 2 S binding to Lucina HbI and mutants of recombinant sperm whale myoglobin. As a cross-check, signs were independently determined from each of the isomorphous replacements in turn. Abstract views Abstract views reflect the number of visits to the article landing page. This charge causes the proteins to repel each other, preventing them from forming clumps that can impede their ability to carry oxygen. Myoglobin typically gives meat and blood its red colour is found in extremely high concentrations in the muscles of mammals that hunt in the deep ocean. Again, this difference is consistent hydrogen bond donation to bound cyanide and acceptance from bound H 2 S.