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Query: NC_017512:52228:59585 Neisseria meningitidis WUE 2594, complete genome

Start: 59585, End: 59689, Length: 105

Host Lineage: Neisseria meningitidis; Neisseria; Neisseriaceae; Neisseriales; Proteobacteria; Bacteria

General Information: The second of two pathogenic Neisseria, this organism causes septicemia and is the leading cause of life-threatening meningitis (inflammation of the meninges, the membrane surrounding the brain and spinal cord) in children. This organism typically residies in the nasopharynx cavity but can invade the respiratory epthelial barrier, cross into the bloodstream and the blood brain barrier, and cause inflammation of the meninges. Pathogenicity factors include the surface proteins (porins and opacity proteins), and the type IV pilus (which is also found in Neisseria gonorrhoeae). This organism, like Neisseria gonorrhoeae, is naturally competent, and protein complexes at the cell surface recognize the uptake signal sequence in extracellular DNA, an 8mer that is found at high frequency in Neisseria chromosomal DNA.

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SubjectStartEndLengthSubject Host DescriptionCDS descriptionE-valueBit score
NC_017505:2192284:220353022035302203724195Neisseria meningitidis alpha710 chromosome, complete genomeputative mafB alternative C-terminus8e-1268.9
NC_010120:2098000:211202621120262112220195Neisseria meningitidis 053442, complete genomeMAFB alternative C-terminus8e-1268.9
NC_003116:291661:299018299018299155138Neisseria meningitidis Z2491, complete genome1e-1168.6
NC_003112:2215184:223245122324512232555105Neisseria meningitidis MC58, complete genomeMafB-related protein1e-1168.6
NC_017513:2134308:214566521456652145859195Neisseria meningitidis G2136 chromosome, complete genomehypothetical protein4e-1063.2
NC_013016:44188:517435174351937195Neisseria meningitidis alpha14 chromosome, complete genomeputative MafB alternative C-terminus4e-1063.2
NC_008767:2126854:214186621418662142060195Neisseria meningitidis FAM18, complete genome4e-1063.2
NC_017501:2219803:223877222387722238876105Neisseria meningitidis 8013, complete genome5e-1063.2