GapMind for catabolism of small carbon sources

 

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

Align Xylose/arabinose import permease protein XylH (characterized, see rationale)
to candidate H281DRAFT_02714 H281DRAFT_02714 monosaccharide ABC transporter membrane protein, CUT2 family

Query= uniprot:Q4J711
         (356 letters)



>FitnessBrowser__Burk376:H281DRAFT_02714
          Length = 331

 Score =  130 bits (327), Expect = 5e-35
 Identities = 97/321 (30%), Positives = 166/321 (51%), Gaps = 27/321 (8%)

Query: 1   MNILNVVRRFEFQLFLVNVIIALFFYFENSAYF-SSNNITTIFQYLAEIGIIAIGEAMLM 59
           +N+L+V       L LV ++I++F     S YF ++NN+  +F+  + I +++IG  +++
Sbjct: 28  LNVLSV-------LLLVGLLISVF-----SPYFLTTNNLMGVFRSFSLIALMSIGMMLVI 75

Query: 60  LCGEIDLSPPALANFVPLITLTIYNSIYQAISPTPAIVVSILLSLGLASLIGLMNGLITT 119
           + G IDLS  ++     L+T  ++   Y A    PA  +   L++G+A  +G  NG + T
Sbjct: 76  ITGGIDLSVGSVMGLSSLVTALVFQHGYNA----PA-AIGAGLAVGIA--VGAFNGFMIT 128

Query: 120 KAKVNSLITTVGTLFLFNGIALIYSGGYPESFPY---FRFLG-GTVSILPVPFIWSLGAL 175
             ++   I T+GTL +  G+  I + G P +      F F+G G +  +P P +  L   
Sbjct: 129 WIQLPPFIATLGTLSIGRGLMYIITKGVPVTPDVPDSFTFIGQGYIGFVPFPVVILLAMT 188

Query: 176 VFLILLLHYTKIGVWTIAAGSNPTGASEVGVPVDRVKIINFIIMANIGALVGIIQGSRVL 235
               +++  T+ G +  A G N   A   GV   RVK   +++   I ++ G+I  SR +
Sbjct: 189 AVFSVVMRQTRFGRYVYATGGNEVAARLSGVRTARVKFTVYVLSGLIASMAGVIAFSRFV 248

Query: 236 TIG-ATNFTADVVLEGIAAAVIGGTSLVGGKGSLVGAFLGSVFISELLNGFNILGINAYE 294
           +   A+ F A+  L+ IAAA IGG SL GG GS+ GA +G+     + NG  +L I+ Y 
Sbjct: 249 SAEPASGFGAE--LDVIAAAAIGGASLSGGAGSVEGAIIGAALAGIITNGVVLLNIDTYA 306

Query: 295 FDAILGGAIVVVMVLSYYAKR 315
             AI G  I++ + +  +  R
Sbjct: 307 QQAITGCVILIAVSIDIWRVR 327


Lambda     K      H
   0.325    0.143    0.404 

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: 319
Number of extensions: 27
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 356
Length of database: 331
Length adjustment: 29
Effective length of query: 327
Effective length of database: 302
Effective search space:    98754
Effective search space used:    98754
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 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