GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01112 in Burkholderia phytofirmans PsJN

Align deoxynucleoside transporter, permease component 2 (characterized)
to candidate BPHYT_RS25785 BPHYT_RS25785 sugar ABC transporter permease

Query= reanno::Burk376:H281DRAFT_01112
         (364 letters)



>FitnessBrowser__BFirm:BPHYT_RS25785
          Length = 352

 Score =  643 bits (1658), Expect = 0.0
 Identities = 331/363 (91%), Positives = 341/363 (93%), Gaps = 12/363 (3%)

Query: 1   MNSRIPSRTDPRTDPPSASPMKQTMTTPTVVEIAPSVEAPGLRTRLARNPEWFTVALIVV 60
           MNSRI SR            + QTMTTPTVVE+AP V+ P LRT+LARNPEWFT+ALI V
Sbjct: 1   MNSRIDSR------------LNQTMTTPTVVEVAPEVKPPSLRTKLARNPEWFTLALIAV 48

Query: 61  TCLIVGAINPRFFQFATLFDLLHSATTMSLFALGTLVVLASGGIDVSFTAIAALTMYGIT 120
           TCLIVGAINPRFFQ ATLFDLLHSATTMSLFALGTLVVLASGGIDVSFTAIAALTMYGIT
Sbjct: 49  TCLIVGAINPRFFQLATLFDLLHSATTMSLFALGTLVVLASGGIDVSFTAIAALTMYGIT 108

Query: 121 KAVFAWWPDAPFALILVTGALGGVVLGMVNGLLVHRLKAPSLIVTIGTQYLYRGLLLTFI 180
           KAVFAWWPDAPFALIL+TGALGGVVLG+VNGLLVHRLKAPSLIVTIGTQYLYRGLLLTFI
Sbjct: 109 KAVFAWWPDAPFALILITGALGGVVLGIVNGLLVHRLKAPSLIVTIGTQYLYRGLLLTFI 168

Query: 181 GTTFFMNIPHSMDRFGRIPLFFYHTADGLRAVLPVSVLALVAAAVVTWWLLNRTMMGRAV 240
           GTTFFMNIPHSMDRFGRIPLFFYHTADGLRAVLPVSV+ALVAAAVVTWWLLNRTMMGR V
Sbjct: 169 GTTFFMNIPHSMDRFGRIPLFFYHTADGLRAVLPVSVVALVAAAVVTWWLLNRTMMGRGV 228

Query: 241 YAMGGSLAIAERLGYNLRAIHLFVFGYTGMLAGIAGILHVSNNRLANPFDLVGSELDVIA 300
           YAMGGSLAIAERLGYNLRAIHLFVFGYTGMLAGIAGILHVSNNRLANPFDLVG+ELDVIA
Sbjct: 229 YAMGGSLAIAERLGYNLRAIHLFVFGYTGMLAGIAGILHVSNNRLANPFDLVGTELDVIA 288

Query: 301 AVILGGARITGGTGTVVGTLLGVVLVTLIKSVLILVGVPSTWQKVIIGAFILLAGTLFAL 360
           AVILGGARITGGTGTV GTLLGVVLVTLI SVLILVGVPSTWQKVIIGAFIL+AGTLFAL
Sbjct: 289 AVILGGARITGGTGTVAGTLLGVVLVTLINSVLILVGVPSTWQKVIIGAFILIAGTLFAL 348

Query: 361 QRK 363
           QRK
Sbjct: 349 QRK 351


Lambda     K      H
   0.328    0.141    0.426 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 533
Number of extensions: 10
Number of successful extensions: 1
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 364
Length of database: 352
Length adjustment: 29
Effective length of query: 335
Effective length of database: 323
Effective search space:   108205
Effective search space used:   108205
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory