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Annotation Overview for fig|1680.3.peg.924 in Bifidobacterium adolescentis:
Phosphoglucosamine mutase (EC 5.4.2.10)

current assignmentPhosphoglucosamine mutase (EC 5.4.2.10)EC Number 5.4.2.10
taxonomy id1680contig
internal linksgenome browser | feature evidence | sequenceACH [?]show essentially identical genes
annotation historyrun tool
FigFamFIG138331
data base cross references
(dbxref)

This feature is part of a subsystem
  • In Sialic Acid Metabolism its role is Phosphoglucosamine mutase (EC 5.4.2.10). However, this subsystem has been classified as not being functional in this organism.
  • In UDP-N-acetylmuramate from Fructose-6-phosphate Biosynthesis its role is Phosphoglucosamine mutase (EC 5.4.2.10).
  • Reasons for Current Assignment

    We have assigned the function "Phosphoglucosamine mutase (EC 5.4.2.10)" to the encoded protein. The protein occurs in 1 subsystem: "UDP-N-acetylmuramate from Fructose-6-phosphate Biosynthesis". In "UDP-N-acetylmuramate from Fructose-6-phosphate Biosynthesis", it appears to play a functional role that we have not associated with any other gene. The function of genes having the same functional roles have been described in Helicobacter pylori (2001995). This is a homologous protein which implements the same function.

    Compare Regions

    The chromosomal region of the focus gene (top) is compared with four similar organisms. The graphic is centered on the focus gene, which is red and numbered 1. Sets of genes with similar sequence are grouped with the same number and color. Genes whose relative position is conserved in at least four other species are functionally coupled and share gray background boxes. The size of the region and the number of genomes may be reset. Click on any arrow in the display to refocus the comparison on that gene. The focus gene always points to the right, even if it is located on the minus strand.






    Topic revision: r6 - 02 Mar 2009 - 22:06:54 - Bruce Parrello
     
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    NMPDR is a collaboration among researchers from the Computation Institute of the University of Chicago, the Fellowship for Interpretation of Genomes (FIG), Argonne National Laboratory, and the National Center for Supercomputing Applications (NCSA) at the University of Illinois. NMPDR is funded by the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services, under Contract HHSN266200400042C. Banner images are copyright © Dennis Kunkel.