The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

Threamine     1-aminopropan-2-ol

Synonyms: Mipa, aminopropanol, CHEMBL326602, NSC-3188, ACMC-1BL70, ...
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

Disease relevance of 2-Propanol, 1-amino-

 

High impact information on 2-Propanol, 1-amino-

  • Thus, an organocobalamin formed by a reaction between the substrate radical and cob(II)alanin is probably not involved in the mechanism of deamination of isopropanolamine by ethanolamine ammonia-lyase [2].
  • This enzyme of subunit molecular weight 19 770 plays a central role in the assembly of the nucleotide loop for adenosylcobalamin where it catalyzes both the phosphorylation of the 1-amino-2-propanol side chain of the corrin ring and the subsequent attachment of GMP to form the product adenosylcobinamide-GDP [3].
  • The cobD mutants appear to be defective in the synthesis of 1-amino-2-propanol, because they can synthesize B12 when this compound is provided exogenously [1].
  • The reaction system is an attractive model for the so far unexplained decarboxylation of threonine to isopropanolamine in the course of corrinoid biosynthesis [4].
 

Analytical, diagnostic and therapeutic context of 2-Propanol, 1-amino-

References

 
WikiGenes - Universities