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Database error: Invalid SQL: select count(id) from pwn_comment where pid='296600' and iffb='1'
MySQL Error: 1194 (Table 'pwn_comment' is marked as crashed and should be repaired)
#0 dbbase_sql->halt(Invalid SQL: select count(id) from pwn_comment where pid='296600' and iffb='1') called at [D:\wwwroot\fcxjsm\includes\db.inc.php:73] #1 dbbase_sql->query(select count(id) from {P}_comment where pid='296600' and iffb='1') called at [D:\wwwroot\fcxjsm\comment\module\CommentContent.php:65] #2 CommentContent() called at [D:\wwwroot\fcxjsm\includes\common.inc.php:518] #3 printpage() called at [D:\wwwroot\fcxjsm\comment\html\index.php:13]
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Warning: mysql_query() [function.mysql-query]: Unable to save result set in D:\wwwroot\fcxjsm\includes\db.inc.php on line 67
Database error: Invalid SQL: select * from pwn_comment where pid='296600' and iffb='1' order by id limit 0,10
MySQL Error: 1194 (Table 'pwn_comment' is marked as crashed and should be repaired)
#0 dbbase_sql->halt(Invalid SQL: select * from pwn_comment where pid='296600' and iffb='1' order by id limit 0,10) called at [D:\wwwroot\fcxjsm\includes\db.inc.php:73] #1 dbbase_sql->query(select * from {P}_comment where pid='296600' and iffb='1' order by id limit 0,10) called at [D:\wwwroot\fcxjsm\comment\module\CommentContent.php:167] #2 CommentContent() called at [D:\wwwroot\fcxjsm\includes\common.inc.php:518] #3 printpage() called at [D:\wwwroot\fcxjsm\comment\html\index.php:13]
Warning: mysql_fetch_array(): supplied argument is not a valid MySQL result resource in D:\wwwroot\fcxjsm\includes\db.inc.php on line 80
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发布于:2019-5-15 09:19:12  访问:40 次 回复: 篇
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Eins getting >1 acetylation internet site. This observation is equivalent to what our
A pairwise comparison of the peak areas for every single set of three biological replicates, with two 4-Aminobutyric acidsupplier technical injection replicates each and every, was then performed (Fig 3B). We implemented our higher threshold standards for the AckA-dependent acetylation web pages to make sure a high amount of self-assurance for these websites. Of proteins with AckA-dependent acetylation sites, 25 had additional than one AckA-dependent acetylation internet site (S6 Table). The typical ackA/wt ratios for lysine acetylation sites ranged from 2.3?6.8 and approximately half in the web-sites showed ratios that were higher than 5 (Fig 4D). The ribosome recycling issue protein (Rrf), the regulator of pilE expression protein (RegF), the phosphoglycerate mutase protein (PgmA), and also the GroES chaperonin ten kDa subunit protein all had a minimum of one acetylation website having a K-acetyl ackA/wt ratio >10 (S6 Table). Parallel experiments from the entire cell lysates PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/20956482 from ackA and wt have been used to examine potential protein level modifications.Eins possessing >1 acetylation web page. This observation is similar to what our group observed in previous E. coli and mitochondria research and suggests that acetylation might have many websites for regulation [23, 48, 54]. 4 proteins had a lot more than 20 acetylation web-sites, such as the chaperonin 60 kDa subunit GroEL protein as well as the chaperone protein DnaK, with 30 and 33 acetylation web pages each, respectively (Fig 4C, S4 Table). GroEL has been previously identified within a quantity of bacteria as one of many most extremely acetylated proteins; nonetheless, the purpose for this high level of acetylation remains unclear [36]. In addition, within a recent critique, it was reported that nearly all of the published bacterial acetylomes showed that GroEL, elongation aspect G (EF-G), and enolase were acetylated [36]. Acetylation web-sites were located in all 3 of those proteins in the existing study, further supporting the idea that acetylation plays a crucial part in these proteins.Label-free quantitation of lysine acetylation sitesMS1 Filtering was employed to quantitatively evaluate the relative abundances from the lysine-acetylation web pages in wt versus ackA samples (Fig 3B). A pairwise comparison in the peak regions for each set of three biological replicates, with two technical injection replicates each, was then performed (Fig 3B). When the ratio between the ackA/wt was >2, at a p-value <0.05, and was found in two or more biological replicates, it was designated as "AckA-dependent" and an average ratio was generated for each site. A total of 109 unique AckA-dependent acetylation sites from 70 unique proteins were detected in this study (S6 Table). Of these sites, 14 met the above AckA-dependent threshold criteria, in all three biological replicates, and 91 sites met the threshold criteria in two biological replicates. The remaining four sites were observed in all three replicates as having an increase in acetylation in 1291ackA compared to 1291wt, but only two of the four replicates met the 2-fold cut-off threshold. None of the AckA-dependent sites had acetylation ratio data that was contradictory to an increase in acetylation of the ackA mutant compared to the wt strain.
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