GapMind for catabolism of small carbon sources

 

Alignments for a candidate for treV in Pseudomonas simiae WCS417

Align TreV, component of Trehalose porter (characterized)
to candidate GFF5028 PS417_25760 spermidine/putrescine ABC transporter ATP-binding protein

Query= TCDB::Q97ZC0
         (324 letters)



>FitnessBrowser__WCS417:GFF5028
          Length = 370

 Score =  224 bits (571), Expect = 3e-63
 Identities = 126/316 (39%), Positives = 184/316 (58%), Gaps = 20/316 (6%)

Query: 8   IVKKY-GKNIVINGITEKIETGEFFVILGPSGEGKSTLLKILAGIEKLDKGKIIADGADI 66
           + K Y G+N+++  +  +I  GEF  +LGPSG GK+T L +LAG E    G+I   G  I
Sbjct: 16  VQKSYDGENLIVKDLNLEIRKGEFLTLLGPSGSGKTTSLMMLAGFETPTAGEIQLAGRSI 75

Query: 67  TDKPPEKRNVAMVFQNYALYPNMSVRDNIAFPLKMRGMKKEEIIERVEKAAKLLGISEIL 126
            + PP KR++ MVFQNYAL+P+M+V +N+AFPL +R + K +I ERV++   ++ +    
Sbjct: 76  NNVPPHKRDIGMVFQNYALFPHMTVAENLAFPLSVRALSKTDISERVKRVLSMVQLDAFA 135

Query: 127 DKKVTQISGGQQQRVALARAIVRNPSYFLLDEPLSNLDARVRTTARGELKRIQKELKGTF 186
            +   Q+SGGQQQRVALARA+V  P   L+DEPL  LD ++R   + E+K + + L  T 
Sbjct: 136 QRYPAQLSGGQQQRVALARALVFEPQLVLMDEPLGALDKQLREHMQMEIKHLHQRLGVTV 195

Query: 187 IYVTHDQKEALSLADRIAILHKGKFEQVSDPKTLYEYPKTKWVAQFVGEFPMNFLPGELM 246
           +YVTHDQ EAL+++DR+A+ H+G+ +Q++ P+TLYE PK  +VA F+GE   N L G L 
Sbjct: 196 VYVTHDQGEALTMSDRVAVFHQGEIQQIAAPRTLYEEPKNTFVANFIGE--NNRLNGRLH 253

Query: 247 KEKAQEI------GFRPEWVEVGKG------NLSCMVESVEASGESRYLICNFKNNNITI 294
               +        G + E + V  G       LS   E V  +G S   +  F       
Sbjct: 254 SHSGERCVVELARGEKVEALAVNVGQVGGPVTLSVRPERVSLNGSSESCVNRFSGR---- 309

Query: 295 LSQEFYDVGQEVRFEI 310
              EF  +G  VR  +
Sbjct: 310 -VAEFIYLGDHVRVRL 324


Lambda     K      H
   0.318    0.137    0.385 

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: 304
Number of extensions: 14
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: 324
Length of database: 370
Length adjustment: 29
Effective length of query: 295
Effective length of database: 341
Effective search space:   100595
Effective search space used:   100595
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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