GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12650 in Burkholderia phytofirmans PsJN

Align D-lactate transporter, permease component 1 (characterized)
to candidate BPHYT_RS19470 BPHYT_RS19470 ABC transporter permease

Query= reanno::Phaeo:GFF1249
         (400 letters)



>FitnessBrowser__BFirm:BPHYT_RS19470
          Length = 323

 Score =  160 bits (404), Expect = 6e-44
 Identities = 106/336 (31%), Positives = 159/336 (47%), Gaps = 52/336 (15%)

Query: 42  YPDLMQRFVIFGIFAIGFNILFGLTGYLSFGHAAFLGVGSYSAVWMFKLLSMNVVPAIVL 101
           YP  + + + F +FA  FN+L G TG LSFGHA FL    Y   +  + L  +    ++ 
Sbjct: 23  YPLFVMKVLCFALFAAAFNLLIGYTGLLSFGHAMFLASAGYVTGYAIQSLGFSPELGVLA 82

Query: 102 SVIVAGLFALVIGYVSLRRSGIYFSILTLAFAQMSFNLAYSVLTPITNGETGLQLTLDDP 161
               A L  L++G  ++RR GIYF+++TLA AQM + +      P T+GE GLQ      
Sbjct: 83  GTAAATLLGLIVGIFAIRRQGIYFAMVTLALAQMVYFVFLQA--PFTHGEDGLQ------ 134

Query: 162 RVLGVSATADGSIPVTSLFG-LEMRSTFEMVVGPWAFQFNAGYYLCALILLAAFYLSIRI 220
                       +P   LFG L++ S   +            Y++   +++ AF L +RI
Sbjct: 135 -----------GVPRGKLFGVLDLSSDVAL------------YFVVLAVMVLAFLLIVRI 171

Query: 221 FRSPFGLMLKAVKSNQQRMNYTGLNTRPYTLAAFVISGMYAGLAGGLMASMDPLAGAERM 280
             SPFG +L A+K N+ R    G +T  + L AF++S   AGLAG L   +         
Sbjct: 172 VHSPFGQVLVAIKENEPRAVSLGYDTDRFKLLAFILSAGIAGLAGSLKVLVQGFETLSDA 231

Query: 281 QWTASGEVVLMTILGGAGTLIGPVLGAGFIKYFENIFSKINDNVLHS----WFSFMPDGI 336
            WT SG V+LMT++GG GTL GP+LGA  I   E+    I   +  +    WF       
Sbjct: 232 YWTMSGLVILMTLVGGMGTLFGPLLGAALIVALEDRLGDIGGALATTTGVEWFR------ 285

Query: 337 EDAMVFIVHPFIGKGWHLTLGILFMLVVIFLPGGLV 372
                      +G+   +  G++F+  V+    G+V
Sbjct: 286 ----------SLGESVTIVTGVIFIACVLAFRRGIV 311


Lambda     K      H
   0.327    0.143    0.435 

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: 425
Number of extensions: 34
Number of successful extensions: 2
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: 400
Length of database: 323
Length adjustment: 29
Effective length of query: 371
Effective length of database: 294
Effective search space:   109074
Effective search space used:   109074
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