"... In PAGE 6: ...1 cache validation requests, and run with a persistent cache on a memory file system to reduce the disk performance problems that we observed. The measurements in Table4 through Table 9 are a consistent set of data taken just before publication. While Jigsaw had outperformed Apache in the first round of tests, Apache now outperforms Jigsaw (which ran interpreted in our tests).... ..."

"... In PAGE 6: ...1 cache validation requests, and run with a persistent cache on a memory file system to reduce the disk performance problems that we observed. The measurements in Table4 through Table 9 are a consistent set of data taken just before publication. While Jigsaw had outperformed Apache in the first round of tests, Apache now outperforms Jigsaw (which ran interpreted in our tests).... ..."

"... In PAGE 3: ... coli asdeterminedfromrandomscreening method.Exactsequences canbefoundin Table1 . (C)Multiple sequence alignment of the N-terminal half of TERT proteins containing the GQ, CP, QFP, and T motifs generated by ClustalW (Chenna et al.... In PAGE 4: ... Plasmid DNA was isolated and sequenced from 27 colonies overexpressing fusion proteins larger than 35 kDa in size. Figure 1B and Table1 summarize the results of this screen. As expected, several of the sequences obtained in the screen were found to have mutations near the N or C terminus of the construct, due to the random nature of the PCR primers used (Table 1) (Kawasaki and Inagaki 2001).... In PAGE 4: ... Figure 1B and Table 1 summarize the results of this screen. As expected, several of the sequences obtained in the screen were found to have mutations near the N or C terminus of the construct, due to the random nature of the PCR primers used ( Table1 ) (Kawasaki and Inagaki 2001). Numerous constructs were found spanning the fingers and part of the palm subdomains of the reverse transcriptase motifs (motifs 1, 2, A, and B) and the region of TERT containing the N-terminal GQ, CP, and QFP motifs.... In PAGE 5: ...) for produc- tion of soluble protein. While performing the expression tests, we noticed that all of the sequences obtained that spanned the GQ motif ( Table1 , colonies 1, 2, 3, 4, and 5) were overexpressed to an exceptionally high level. We therefore focused on this region of TERT in order to validate that the high- throughput assay was indeed identifying regions of the protein that could be expressed in a soluble form and purified with a high yield.... ..."