htpX:Quickview: Difference between revisions
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!align=left {{table_heading_style}} | | !align=left {{table_heading_style}} |Standard Name | ||
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!align=left {{table_heading_style}} | | !align=left {{table_heading_style}} |Gene Synonym(s) | ||
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!align=left {{table_heading_style}} | | !align=left {{table_heading_style}} |Product Desc. | ||
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!align=left {{table_heading_style}} |Knock-Out Phenotype | !align=left {{table_heading_style}} |Knock-Out Phenotype | ||
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!align=left {{table_heading_style}} |Regulation/Expression | !align=left {{table_heading_style}} |Regulation/Expression | ||
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!align=left {{table_heading_style}} |Regulation/Activity | !align=left {{table_heading_style}} |Regulation/Activity | ||
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Revision as of 20:49, 4 March 2009
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| Quickview | Gene | Gene Product(s) | Expression | Evolution | On One Page |
| References | Suggestions |
See Help:Quickview for help with entering information in the Quickview table.
| Standard Name |
|---|
| Gene Synonym(s) |
| Product Desc. |
| Product Synonyms(s) |
| Knock-Out Phenotype |
| Regulation/Expression |
| Regulation/Activity |
| edit table |
See Help:Quickview for help with entering information in the Quickview table.
Notes
Overexpression of truncated HtpX promotes degradation of incomplete proteins in puromycin-treated cells. HtpX collaborates with FtsH to eliminate abnormal membrane proteins: an hflX ftsH double mutant is temperature-sensitive for growth. Inactivation of putative protease active site residues abolishes ability to cross-complement defects in the FtsH protease. Start codon verified by toeprint analysis (Kornitzer, 1991). HtpX has a cytosolic active site. HtpX in vivo cleavage of SecY is seen when both are overproduced. Cpx regulon. RpoH regulon. Synthetic lethal with hflB(ftsH) in fabZ(SfhC) background. HtpX has two TM helices. htpX, yggG, yfgC and ycaL are paralogs.[1]
References