Difference between revisions of "MsmX"
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|style="background:#ABCDEF;" align="center"|'''Function''' || maltodextrin uptake | |style="background:#ABCDEF;" align="center"|'''Function''' || maltodextrin uptake | ||
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| + | |colspan="2" style="background:#FAF8CC;" align="center"| '''Metabolic function and regulation of this protein in [[SubtiPathways|''Subti''Pathways]]: <br/>[http://subtiwiki.uni-goettingen.de/pathways/carbohydrate_metabolic_pathways.html Sugar catabolism]''' | ||
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|style="background:#ABCDEF;" align="center"| '''MW, pI''' || 41 kDa, 7.385 | |style="background:#ABCDEF;" align="center"| '''MW, pI''' || 41 kDa, 7.385 | ||
Revision as of 12:01, 11 June 2009
- Description: multiple sugar-binding transport ATP-binding protein
| Gene name | msmX |
| Synonyms | yxkG |
| Essential | no |
| Product | multiple sugar-binding transport ATP-binding protein |
| Function | maltodextrin uptake |
| Metabolic function and regulation of this protein in SubtiPathways: Sugar catabolism | |
| MW, pI | 41 kDa, 7.385 |
| Gene length, protein length | 1095 bp, 365 aa |
| Immediate neighbours | yxkH, yxkF |
| Get the DNA and protein sequences (Barbe et al., 2009) | |
Genetic context
This image was kindly provided by SubtiList
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Contents
The gene
Basic information
- Locus tag: BSU38810
Phenotypes of a mutant
Database entries
- DBTBS entry: no entry
- SubtiList entry: [1]
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity:
- Protein family: ABC transporter family (according to Swiss-Prot)
- Paralogous protein(s):
Extended information on the protein
- Kinetic information:
- Domains:
- Modification:
- Cofactor(s):
- Effectors of protein activity:
- Interactions:
- Localization: cell membrane (according to Swiss-Prot)
Database entries
- Structure:
- Swiss prot entry: P94360
- KEGG entry: [2]
- E.C. number:
Additional information
Expression and regulation
- Regulation: repressed by glucose (CcpA)
- Regulatory mechanism: CcpA: transcription repression
- Additional information:
Biological materials
- Mutant:
- Expression vector:
- lacZ fusion:
- GFP fusion:
- two-hybrid system:
- Antibody:
Labs working on this gene/protein
Your additional remarks
References
- Author1, Author2 & Author3 (year) Title Journal volume: page-page. PubMed
