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【期刊论文】Structural genomics efforts at the Chinese Academy of Sciences and Peking University
苏晓东, W.M. Gong, H.Y. Liu, L.W. Niu, Y.Y. Shi, *, Y.J. Tang, M.K. Teng, J.H. Wu, D.C. Liang, D.C. Wang, J.F. Wang, J.P. Ding, H.Y. Hu, Q.H. Huang, Q.H. Zhang, S.Y. Lu, J.L. An, Y.H. Liang, X.F. Zheng, X.C. Gu & X.D. Su
Journal of Structural and Functional Genomics 4: 137-139, 2003.,-0001,():
-1年11月30日
Structural genomics efforts at the Chinese Academy of Sciences and Peking University are reported in this article. The major targets for the structural genomics project are targeted proteins expressed in human hematopoietic stem/progenitor cells, proteins related to blood diseases and other human proteins. Up to now 328 target genes have been constructed in expression vectors. Among them, more than 50% genes have been expressed in Escherichia coli, approximately 25% of the resulting proteins are soluble, and 35 proteins have been purified. Crystallization, data collection and structure determination are continuing. Experiences accumulated during this initial stage are useful for designing and applying high-throughput approaches in structural genomics.
blood disease,, hematopoietic stem/, progenitor cells,, nuclear magnetic resonance,, protein structure,, structural genomics,, X-ray rystallography
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苏晓东, Shahrzad Bakhtiar, a Jitka VeÂvodovaÂ, b† Rajni Hatti-Kaul a and Xiao-Dong Sub *
Acta Cryst. (2003). D59, 529-531,-0001,():
-1年11月30日
A novel calcium-independent serine protease from an alkaliphilic bacterium, Nesterenkonia sp. AL20, has been purified and crystallized at 296 Kusing sodium formate as the main precipitant. This enzyme is optimally active at pH 10, exhibits high stability towards autolytic digestion and its stability is not affected by the presence of EDTA or detergents. The triangular prism-shaped crystals diffracted X-rays to beyond 1.5 A
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苏晓东, Martin E. Andersson, ‡, # Martin Hogbom, §, # Agnes Rinaldo-Matthis, ‡ Wolfgang Blodig, ‡ Yuhe Liang, || Bert-Ove Persson, ┴ Britt-Marie Sjoberg, ┴ Xiao-Dong Su, || and Pär Nordlund *
Biochemistry 2004, 43, 7966-7972,-0001,():
-1年11月30日
The R2 protein of ribonucleotide reductase features a di-iron site deeply buried in the protein interior. The apo form of the R2 protein has an unusual clustering of carboxylate side chains at the empty metal-binding site. In a previous study, it was found that the loss of the four positive charge equivalents of the diferrous site in the apo protein appeared to be compensated for by the protonation of two histidine and two carboxylate side chains. We have studied the consequences of removing and introducing charged residues on the local hydrogen-bonding pattern in the region of the carboxylate cluster of Corynebacterium ammoniagenes and Escherichia coli protein R2 using site-directed mutagenesis and X-ray crystallography. The structures of the metal-free forms of wild-type C. ammoniagenes R2 and the mutant E. coli proteins D84N, S114D, E115A, H118A, and E238A have been determined and their hydrogen bonding and protonation states have been structurally assigned as far as possible. Significant alterations to the hydrogenbonding patterns, protonation states, and hydration is observed for all mutant E. coli apo proteins as compared to wild-type apo R2. Further structural variations are revealed by the wild-type apo C. ammoniagenes R2 structure. The protonation and hydration effects seen in the carboxylate cluster appear to be due to two major factors: conservation of the overall charge of the site and the requirement of electrostatic shielding of clustered carboxylate residues. Very short hydrogen-bonding distances between some protonated carboxylate pairs are indicative of low-barrier hydrogen bonding.
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苏晓东
,-0001,():
-1年11月30日
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苏晓东
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-1年11月30日
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