GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Paraburkholderia bryophila 376MFSha3.1

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate H281DRAFT_02714 H281DRAFT_02714 monosaccharide ABC transporter membrane protein, CUT2 family

Query= uniprot:A0A1N7UKA9
         (325 letters)



>FitnessBrowser__Burk376:H281DRAFT_02714
          Length = 331

 Score =  277 bits (709), Expect = 2e-79
 Identities = 139/315 (44%), Positives = 205/315 (65%), Gaps = 1/315 (0%)

Query: 12  AAPRNRLRLSLDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYV 71
           AA   R  L +    +  V +L+ ++++  S YF+T  N M + R  S+  ++++GM  V
Sbjct: 15  AADWIRACLRIRELNVLSVLLLVGLLISVFSPYFLTTNNLMGVFRSFSLIALMSIGMMLV 74

Query: 72  ILTKGIDLSVGSILAFAGLCSAMVATQGYGLLAAVSAGMFAGAMLGVVNGFMVANLSIPP 131
           I+T GIDLSVGS++  + L +A+V   GY   AA+ AG+  G  +G  NGFM+  + +PP
Sbjct: 75  IITGGIDLSVGSVMGLSSLVTALVFQHGYNAPAAIGAGLAVGIAVGAFNGFMITWIQLPP 134

Query: 132 FVATLGMLSIARGMTFILNDGSPIT-DLPDAYLALGIGKIGPIGVPIIIFAVVALIFWMV 190
           F+ATLG LSI RG+ +I+  G P+T D+PD++  +G G IG +  P++I   +  +F +V
Sbjct: 135 FIATLGTLSIGRGLMYIITKGVPVTPDVPDSFTFIGQGYIGFVPFPVVILLAMTAVFSVV 194

Query: 191 LRYTTYGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQA 250
           +R T +GRYVYA GGNE +AR SG+   +V F+VYV+SGL+A +AGV+  +R  SA P +
Sbjct: 195 MRQTRFGRYVYATGGNEVAARLSGVRTARVKFTVYVLSGLIASMAGVIAFSRFVSAEPAS 254

Query: 251 GVSYELDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLGVSSYYQQVAKGLI 310
           G   ELD IAA  IGG SLSGG GS+ G + GA L G+I NG+ LL + +Y QQ   G +
Sbjct: 255 GFGAELDVIAAAAIGGASLSGGAGSVEGAIIGAALAGIITNGVVLLNIDTYAQQAITGCV 314

Query: 311 IVFAVLIDVWRKKKR 325
           I+ AV ID+WR +++
Sbjct: 315 ILIAVSIDIWRVRRK 329


Lambda     K      H
   0.326    0.141    0.412 

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: 263
Number of extensions: 9
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: 325
Length of database: 331
Length adjustment: 28
Effective length of query: 297
Effective length of database: 303
Effective search space:    89991
Effective search space used:    89991
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 (21.6 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