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Summary[edit | edit source]

  • pan ID?: SAUPAN005498000
  • symbol?: mtlF
  • synonym:
  • description?: mannitol-specific phosphotransferase enzyme IIA component

      descriptions from strain specific annotations:

    • mannitol-specific phosphotransferase enzyme IIA component
    • PTS system, mannitol-specific IIA component
    • PTS system mannitol specific transporter subunit IIA
    • mannitol-specific IIA component
    • PTS mannitol transporter subunit IIA
    • PTS sugar transporter subunit IIA
    • PTS system, mannitol specific IIA component, putative
    • mannitol-specific phosphotransferase enzyme IIA component (PTS system mannitol-specific EIIA component) (EIIA-Mtl) (EIII-Mtl)
    • PTS system mannitol specific IIA component
    • phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2
    • phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2, MtlA_1
    • phosphoenolpyruvate-dependent sugar phosphotransferase system EIIA 2
    • PTS family fructose/mannitol (fru) porter component IIA
    • PTS family mannitol porter, IIA component
  • strand?: +
  • coordinates?: 5654851..5655295
  • synteny block?: BlockID0042800
  • occurrence?: in 100% of 34 strains

mtlF : mannitol-specific phosphotransferase system IIA MtlF [1]

In addition to its role as a carbon source, mannitol is a compatible solute that can impact the osmotic balance of the staphylococcal cell. Therefore, mannitol transportation by phosphotransferase systems can be critical to staphylococcal viability. Phosphotransferase systems couple sugar transport to sugar phosphorylation which traps the substrate in the cytoplasm. All phosphotransferase systems share the common transfer of activated phosphate from phosphoenolpyruvate to Complex EI and then on to the soluble phosphocarrier protein HPr. HPr can then transfer its phosphate to sugar-specific complex EIIA (acceptor-activator) and EIIBC (kinase-transporter) subunits. Mannitol-specific IIA and IIBC subunits are encoded by mtlF and mtlA, respectively. Please note, some annotations describe the mannitol transport operon with MtlF as the IIBC component and MtlA as the IIA component. For consistency with the majority of firmicute annotations, we will here annotate the IIBC component as "MtlA" and the IIA component as "MtlF".

Orthologs[edit | edit source]

    COL:
    N315:
    SA1962 (mtlA)
    NCTC8325:
    Newman:
    NWMN_2059 (mtlA)
    USA300_FPR3757:
    04-02981:
    SA2981_2097 (mtlA)
    08BA02176:
    C248_2186 (mtlF)
    11819-97:
    MS7_2173 (mtlF)
    6850:
    RSAU_001994 (mtlA)
    71193:
    ST398NM01_2213
    ECT-R 2:
    ECTR2_2011
    ED133:
    SAOV_2197
    ED98:
    SAAV_2212
    HO 5096 0412:
    SAEMRSA15_20640 (mtlF)
    JH1:
    SaurJH1_2228
    JH9:
    SaurJH9_2190
    JKD6008:
    SAA6008_02194 (mtlA_1)
    JKD6159:
    SAA6159_02067 (mtlA_1)
    JSNZ:
    JSNZ_002118
    LGA251:
    SARLGA251_19540 (mtlF)
    M013:
    M013TW_2116
    MRSA252:
    SAR2246 (mtlF)
    MSHR1132:
    SAMSHR1132_19900
    MSSA476:
    SAS2059
    Mu3:
    SAHV_2142 (mtlA)
    Mu50:
    SAV2158 (mtlA)
    MW2:
    MW2084 (mtlA)
    RF122:
    SAB2038 (mtlF)
    ST398:
    SAPIG2213
    T0131:
    SAT0131_02321
    TCH60:
    HMPREF0772_11035 (mtlF)
    TW20:
    SATW20_22930 (mtlF)
    USA300_TCH1516:
    USA300HOU_2148 (mtlA)
    VC40:
    SAVC_09655

Genome Viewer[edit | edit source]

COL
N315
NCTC8325
Newman
USA300_FPR3757

Alignments[edit | edit source]

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


    COL             MSELFSNDNIFLNVNVNSQNEAIEKAGKALVDSGAVTDAYIQAMKDREQVVSTFMGNGLA
    N315            MSELFSNDNIFLNVNVNSQNEAIEKAGKALVDSGAVTDAYIQAMKDREQVVSTFMGNGLA
    NCTC8325        MSELFSNDNIFLNVNVNSQNEAIEKAGKALVDSGAVTDAYIQAMKDREQVVSTFMGNGLA
    Newman          MSELFSNDNIFLNVNVNSQNEAIEKAGKALVDSGAVTDAYIQAMKDREQVVSTFMGNGLA
    USA300_FPR3757  MSELFSNDNIFLNVNVNSQNEAIEKAGKALVDSGAVTDAYIQAMKDREQVVSTFMENGLA
                    ******************************************************* ****

    COL             IPHGTDEAKTNVIHSGLTLLQIPEGVDWDGEVVKVVVGIAGKDGEHLDLLSKIAITFSEE
    N315            IPHGTDEAKTNVIHSGLTLLQIPEGVDWDGEVVKVVVGIAGKDGEHLDLLSKIAITFSEE
    NCTC8325        IPHGTDEAKTNVIHSGLTLLQIPEGVDWDGEVVKVVVGIAGKDGEHLDLLSKIAITFSEE
    Newman          IPHGTDEAKTNVIHSGLTLLQIPEGVDWDGEVVKVVVGIAGKDGEHLDLLSKIAITFSEE
    USA300_FPR3757  IPHGTDEAKTNVIHSGLTLLQIPEGVDWDGEVVKVVVGIAGKDGEHLDLLSKIAITFSEE
                    ************************************************************

    COL             ENVDRIVQAKSAEEIKQVFEEADA
    N315            ENVDRIVQAKSAEEIKQVFEEADA
    NCTC8325        ENVDRIVQAKSAEEIKQVFEEADA
    Newman          ENVDRIVQAKSAEEIKQVFEEADA
    USA300_FPR3757  ENVDRIVQAKSAEEIKQVFEEADA
                    ************************

  1. Nicholas P Vitko, Melinda R Grosser, Dal Khatri, Thurlow R Lance, Anthony R Richardson
    Expanded Glucose Import Capability Affords Staphylococcus aureus Optimized Glycolytic Flux during Infection.
    mBio: 2016, 7(3);
    [PubMed:27329749] [WorldCat.org] [DOI] (I e)
    Thanh Nguyen, Truc Kim, Hai Minh Ta, Won Sik Yeo, Jongkeun Choi, Pushpak Mizar, Seung Seo Lee, Taeok Bae, Akhilesh Kumar Chaurasia, Kyeong Kyu Kim
    Targeting Mannitol Metabolism as an Alternative Antimicrobial Strategy Based on the Structure-Function Study of Mannitol-1-Phosphate Dehydrogenase in Staphylococcus aureus.
    mBio: 2019, 10(4);
    [PubMed:31289190] [WorldCat.org] [DOI] (I e)