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Summary[edit | edit source]

  • pan ID?: SAUPAN004077000
  • symbol?: xseB
  • synonym:
  • description?: exodeoxyribonuclease VII small subunit

      descriptions from strain specific annotations:

    • exodeoxyribonuclease VII small subunit
    • exodeoxyribonuclease 7 small subunit
    • exodeoxyribonuclease VII, small subunit, putative
    • exodeoxyribonuclease VII, small subunit
    • putative exodeoxyribonuclease VII small subunit
  • strand?: -
  • coordinates?: 4359466..4359696
  • synteny block?: BlockID0031090
  • occurrence?: in 97% of 34 strains

xseB : exodeoxyribonuclease VII small subunit [1]

Staphylococci require degradation of single-stranded DNA for multiple cellular processes including DNA mismatch repair, homologous recombination and antiviral defenses. The XseAB system (ExoVII) is a bi-directional (3'→5' or 5'→3') exoDNase that can degrade single-stranded DNA. Typically, incorrect base pairing during replication is detected by MutS which recruits the MutL repair center protein. Unlike in E. coli which uses a separate nickase enzyme (MutH), staphylococcal MutL has a separate domain to nick the unmethylated strand at its hemimethylated GATC recognition site. DNA is unwound, typically by PcrA helicase, and, depending on the location of the nick, a 3'→5' or 5'→3' ssDNA exodeoxyribonuclease is required to depolymerize the non-methylated strand. While RecJ can perform 5'→3' processing, only ExoVII can degrade ssDNA in either orientation.

Orthologs[edit | edit source]

    COL:
    SACOL1567 (xseB)
    N315:
    NCTC8325:
    Newman:
    USA300_FPR3757:
    04-02981:
    SA2981_1481
    08BA02176:
    C248_1565
    11819-97:
    MS7_1540 (xseB)
    6850:
    RSAU_001389 (xseB)
    71193:
    ST398NM01_1588
    ECT-R 2:
    ECTR2_1374 (xseB)
    ED133:
    SAOV_1523 (xseB)
    ED98:
    SAAV_1515 (xseB)
    HO 5096 0412:
    SAEMRSA15_14430
    JH1:
    SaurJH1_1614
    JH9:
    SaurJH9_1581
    JKD6008:
    SAA6008_01492 (xseB)
    JKD6159:
    SAA6159_01458 (xseB)
    JSNZ:
    JSNZ_001513
    LGA251:
    SARLGA251_14290
    M013:
    M013TW_1538
    MRSA252:
    SAR1600
    MSHR1132:
    SAMSHR1132_13630
    MSSA476:
    SAS1461
    Mu3:
    SAHV_1510
    Mu50:
    SAV1522
    MW2:
    MW1475
    RF122:
    SAB1395c
    ST398:
    SAPIG1588 (xseB)
    T0131:
    SAT0131_01616
    TCH60:
    HMPREF0772_11618 (xseB)
    TW20:
    SATW20_15190
    USA300_TCH1516:
    USA300HOU_1524 (xseB)
    VC40:
    SAVC_06860

Genome Viewer[edit | edit source]

COL
N315
NCTC8325
USA300_FPR3757

Alignments[edit | edit source]

  • alignment of orthologues:
    CLUSTAL format alignment by MAFFT L-INS-i (v7.307)


    COL             MTKETQSFEEMMQELEQIVQKLDNETVSLEESLDLYQRGMKLSAACDTTLKNAEKKVNDL
    N315            MTKETQSFEEMMQELEQIVQKLDNETVSLEESLDLYQRGMKLSAACDTTLKNAEKKVNDL
    NCTC8325        MTKETQSFEEMMQELEQIVQKLDNETVSLEESLDLYQRGMKLSAACDTTLKNAEKKVNDL
    USA300_FPR3757  MTKETQSFEEMMQELEQIVQKLDNETVSLEESLDLYQRGMKLSAACDTTLKNAEKKVNDL
                    ************************************************************

    COL             IKEEAEDVKNDESTDE
    N315            IKEEAEDVKNDESTDE
    NCTC8325        IKEEAEDVKNDESTDE
    USA300_FPR3757  IKEEAEDVKNDESTDE
                    ****************

  1. Katarzyna Poleszak, Katarzyna H Kaminska, Stanislaw Dunin-Horkawicz, Andrei Lupas, Krzysztof J Skowronek, Janusz M Bujnicki
    Delineation of structural domains and identification of functionally important residues in DNA repair enzyme exonuclease VII.
    Nucleic Acids Res: 2012, 40(16);8163-74
    [PubMed:22718974] [WorldCat.org] [DOI] (I p)
    Susan T Lovett
    The DNA Exonucleases of Escherichia coli.
    EcoSal Plus: 2011, 4(2);
    [PubMed:26442508] [WorldCat.org] [DOI] (P p)
    Liping Liu, Hanne Ingmer, Martin Vestergaard
    Genome-Wide Identification of Resveratrol Intrinsic Resistance Determinants in Staphylococcus aureus.
    Antibiotics (Basel): 2021, 10(1);
    [PubMed:33467002] [WorldCat.org] [DOI] (P e)