GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01112 in Pseudomonas simiae WCS417

Align deoxynucleoside transporter, permease component 2 (characterized)
to candidate GFF2365 PS417_12060 sugar ABC transporter permease

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



>FitnessBrowser__WCS417:GFF2365
          Length = 325

 Score =  147 bits (372), Expect = 3e-40
 Identities = 102/334 (30%), Positives = 171/334 (51%), Gaps = 20/334 (5%)

Query: 34  APSVEAPGLRTRLARNPEWFTVALIVVTCLIVGAINPRFFQ-FATLFDLLHSATTMSLFA 92
           AP   AP  R RL  + + F + L+ +   +V A +  +F  +    D+L   +   + A
Sbjct: 8   APVTAAP--RNRLRLSLDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTSINGILA 65

Query: 93  LGTLVVLASGGIDVSFTAIAALTMYGITKAVFAWWPDAPFALILVTGALGGVVLGMVNGL 152
           +G   V+ + GID+S  +I A    G+  A+ A       A +   G   G +LG+VNG 
Sbjct: 66  VGMTYVILTKGIDLSVGSILAFA--GLCSAMVATQGYGLLAAVSA-GMFAGAMLGVVNGF 122

Query: 153 LVHRLKAPSLIVTIGTQYLYRGLLLTFIGTTFFMNIPHSMDRFGRIPLFFYHTADGLRAV 212
           +V  L  P  + T+G   + RG+       +   ++P +            + A G+  +
Sbjct: 123 MVANLSIPPFVATLGMLSIARGMTFILNDGSPITDLPDA------------YLALGIGKI 170

Query: 213 LPVSVLALVAA--AVVTWWLLNRTMMGRAVYAMGGSLAIAERLGYNLRAIHLFVFGYTGM 270
            P+ V  ++ A  A++ W +L  T  GR VYA+GG+   A   G  +R +   V+  +G+
Sbjct: 171 GPIGVPIIIFAVVALIFWMVLRYTTYGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSGL 230

Query: 271 LAGIAGILHVSNNRLANPFDLVGSELDVIAAVILGGARITGGTGTVVGTLLGVVLVTLIK 330
           LAG+AG++  +    A P   V  ELD IAAV++GG  ++GGTG++VGTL G +L+ +I 
Sbjct: 231 LAGLAGVVLSARTTSALPQAGVSYELDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVIN 290

Query: 331 SVLILVGVPSTWQKVIIGAFILLAGTLFALQRKR 364
           + L L+GV S +Q+V  G  I+ A  +   ++K+
Sbjct: 291 NGLNLLGVSSYYQQVAKGLIIVFAVLIDVWRKKK 324


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: 268
Number of extensions: 8
Number of successful extensions: 3
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: 325
Length adjustment: 29
Effective length of query: 335
Effective length of database: 296
Effective search space:    99160
Effective search space used:    99160
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