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Structural analysis of a set of proteins resulting from a bacterial genomics project 总被引:1,自引:0,他引:1
Badger J Sauder JM Adams JM Antonysamy S Bain K Bergseid MG Buchanan SG Buchanan MD Batiyenko Y Christopher JA Emtage S Eroshkina A Feil I Furlong EB Gajiwala KS Gao X He D Hendle J Huber A Hoda K Kearins P Kissinger C Laubert B Lewis HA Lin J Loomis K Lorimer D Louie G Maletic M Marsh CD Miller I Molinari J Muller-Dieckmann HJ Newman JM Noland BW Pagarigan B Park F Peat TS Post KW Radojicic S Ramos A Romero R Rutter ME Sanderson WE Schwinn KD Tresser J Winhoven J Wright TA Wu L Xu J Harris TJ 《Proteins》2005,60(4):787-796
The targets of the Structural GenomiX (SGX) bacterial genomics project were proteins conserved in multiple prokaryotic organisms with no obvious sequence homolog in the Protein Data Bank of known structures. The outcome of this work was 80 structures, covering 60 unique sequences and 49 different genes. Experimental phase determination from proteins incorporating Se-Met was carried out for 45 structures with most of the remainder solved by molecular replacement using members of the experimentally phased set as search models. An automated tool was developed to deposit these structures in the Protein Data Bank, along with the associated X-ray diffraction data (including refined experimental phases) and experimentally confirmed sequences. BLAST comparisons of the SGX structures with structures that had appeared in the Protein Data Bank over the intervening 3.5 years since the SGX target list had been compiled identified homologs for 49 of the 60 unique sequences represented by the SGX structures. This result indicates that, for bacterial structures that are relatively easy to express, purify, and crystallize, the structural coverage of gene space is proceeding rapidly. More distant sequence-structure relationships between the SGX and PDB structures were investigated using PDB-BLAST and Combinatorial Extension (CE). Only one structure, SufD, has a truly unique topology compared to all folds in the PDB. 相似文献
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Site-specific recombination on supercoiled circular DNA yields a variety of knotted or catenated products. Here, we present a topological model of this process and characterize all possible products of the most common substrates: unknots, unlinks, and torus knots and catenanes. This model tightly prescribes the knot or catenane type of previously uncharacterized data. We also discuss how the model helps to distinguish products of distributive recombination and, in some cases, determine the order of processive recombination products. 相似文献
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Recently, a number of articles have been published on the mechanisms of dental development, and in particular on the genetic control of dental formation. As a specific example of the potential of this kind of research for paleoanthropological studies, cusp areas of upper molars of two species of South African Australopithecines (Australopithecus africanus, A. robustus) have been examined. The results suggest notable differences between the two species, possibly related to markedly different developmental pathways that are still far from clear in their details. 相似文献