Difference between revisions of "IolG"
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* '''Kinetic information:''' | * '''Kinetic information:''' | ||
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* '''Modification:''' | * '''Modification:''' | ||
| − | * ''' | + | * '''[[Cofactors]]:''' NAD<sup>+</sup> {{PubMed|20809899}} |
* '''Effectors of protein activity:''' | * '''Effectors of protein activity:''' | ||
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| − | <pubmed>9226270,6322857,1761221,112095,,9887260,18310071 112095 20809899 23952058 </pubmed> | + | <pubmed>9226270,6322857,1761221,112095,,9887260,18310071 112095 20809899 23952058 24325193 </pubmed> |
[[Category:Protein-coding genes]] | [[Category:Protein-coding genes]] | ||
Revision as of 17:56, 13 December 2013
- Description: inositol 2-dehydrogenase
| Gene name | iolG |
| Synonyms | idh, iol |
| Essential | no |
| Product | inositol 2-dehydrogenase |
| Function | myo-inositol catabolism |
| Gene expression levels in SubtiExpress: iolG | |
| Metabolic function and regulation of this protein in SubtiPathways: Sugar catabolism | |
| MW, pI | 38 kDa, 4.865 |
| Gene length, protein length | 1032 bp, 344 aa |
| Immediate neighbours | iolH, iolF |
| Sequences | Protein DNA DNA_with_flanks |
Genetic context 
This image was kindly provided by SubtiList
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Expression at a glance PubMed
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Contents
Categories containing this gene/protein
utilization of specific carbon sources
This gene is a member of the following regulons
The gene
Basic information
- Locus tag: BSU39700
Phenotypes of a mutant
Database entries
- DBTBS entry: [1]
- SubtiList entry: [2]
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity: Myo-inositol + NAD+ = 2,4,6/3,5-pentahydroxycyclohexanone + NADH (according to Swiss-Prot)
- Protein family: gfo/idh/mocA family (according to Swiss-Prot)
Extended information on the protein
- Kinetic information:
- Modification:
- Effectors of protein activity:
- Interactions:
- the protein forms a tetramer PubMed
Database entries
- UniProt: P26935
- KEGG entry: [3]
- E.C. number: 1.1.1.18
Additional information
Expression and regulation
- Additional information:
Biological materials
- Mutant:
- Expression vector:
- lacZ fusion:
- GFP fusion:
- two-hybrid system:
- Antibody:
Labs working on this gene/protein
- Yasutaro Fujita, University of Fukuyama, Japan
- Ken-ichi Yoshida, Kobe University, Japan
Your additional remarks
References
