Escherichia coli K-12 GenePage Master Page of yaaW
GenePage for the
yaaW
gene of
Escherichia coli
K-12
2DBase: P75617
Bacteriome: yaaW
CMR: P75617
COG: COG4735
ColiBASE: b0011
Colibri: yaaW
Doodle: yaaW
EchoBASE: EB4086
ECID: P75617
EcoliWiki: yaaW
GenExpDB: b0011
GenomeReviews: b0011
GenProtEC: b0011
GTOP: yaaW
KEGG: b0011
MiST: b0011
ModBase: P75617
Operon: 31299
PairsDB: P75617
Pedant: 10
Pfam: P75617
ProDom: P75617
ProtoNet: P75617
RefSeq: 16128005
SWISS-2D: P75617
Swiss-Prot: P75617
TIGR-CMR: NT01EC0012
TIGRHmm: NT01EC0012
Uber-Operon: 2461
Primary Gene Name:
yaaW
EcoGene Accession Number: EG14340
K-12 Gene Accession Number: ECK0011
MG1655 Gene Identifier:
b0011
Horizontal Gene Transfer
HT1006
Y-genes
Gene Name Mnemonic: Systematic nomenclature
Alternate Gene Symbols: htgA, htpY
DNA Sequence
  # bp Upstream
# bp Downstream
Description:
Conserved protein, UPF0174 family
Pre-Run BlastP UniProt
Protein Sequence:
------------ MW: 26664.88------237 aa ------------
Pre-Run BlastP NR+Env
Genomic Address
Left End: 10643 ----------------- Counterclockwise ----------------- Right End: 11356
Left Inter Gene Info
Minute or Centisome (%) = 0.23
Right Inter Gene Info
 
gene or min(Cs)
PDF EcoMap
Curator or user-submitted Comments:
htgA was described as an an ORF on the opposite strand of yaaW, but the relationships among yaaW, htgA and htpY need to be reexamined. yaaW has homologs and looks like a protein-coding gene, whereas the ORF on the opposite strand once labeled htgA does not look like a protein coding gene. It is possible that there is a heat-inducible anti-sense regulatory RNA on the opposite strand of yaaW, but it is unlikely that this putative transcript would encode a functional protein product. A reexaminination shows no heat shock induction or Sigma 32 expression of htgA, consistent with it not being a gene or protein at all (Nonaka, 2006). Mutations in the opposite ORF would also disrupt yaaW and hence the htgA and htpY gene names are used as synonyms for yaaW. The experimental evidence supporting the existence of htgA is likely to be in error and the conclusions of Delaye (2008) regarding evolution of overlapping genes is unlikely to be true; their homology analysis and their analysis of substitutions within htgA are all consistent with htgA being an incorrect annotation; extreme skepticism is warranted when studying supposedly overlapping genes that do not appear to be phage-related in the E. coli chromsome.
Copyright 2006 University of Miami.
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