GapMind for catabolism of small carbon sources

 

Aligments for a candidate for treV in Escherichia coli BW25113

Align TreV, component of Trehalose porter (characterized)
to candidate 15562 b1441 predicted spermidine/putrescine transporter subunit (NCBI)

Query= TCDB::Q97ZC0
         (324 letters)



>lcl|FitnessBrowser__Keio:15562 b1441 predicted
           spermidine/putrescine transporter subunit (NCBI)
          Length = 337

 Score =  212 bits (540), Expect = 9e-60
 Identities = 118/302 (39%), Positives = 186/302 (61%), Gaps = 10/302 (3%)

Query: 3   VELIDIVKKYGKNIVINGITEKIETGEFFVILGPSGEGKSTLLKILAGIEKLDKGKIIAD 62
           VE  ++ + YG    ++G++  I+ GEFF +LGPSG GK+T L+++AG E+L  G I   
Sbjct: 5   VEFDNVSRLYGDVRAVDGVSIAIKDGEFFSMLGPSGSGKTTCLRLIAGFEQLSGGAISIF 64

Query: 63  GADITDKPPEKRNVAMVFQNYALYPNMSVRDNIAFPLKMRGMKKEEIIERVEKAAKLLGI 122
           G   ++ PP +R+V  VFQ+YAL+P+MS+ DN+A+ L ++G+ K++     ++A + + +
Sbjct: 65  GKPASNLPPWERDVNTVFQDYALFPHMSILDNVAYGLMVKGVNKKQRHAMAQEALEKVAL 124

Query: 123 SEILDKKVTQISGGQQQRVALARAIVRNPSYFLLDEPLSNLDARVRTTARGELKRIQKEL 182
             +  +K +Q+SGGQ+QRVA+ARA+V  P   LLDEPL  LD ++R   + ELK++Q+ L
Sbjct: 125 GFVHQRKPSQLSGGQRQRVAIARALVNEPRVLLLDEPLGALDLKLREQMQLELKKLQQSL 184

Query: 183 KGTFIYVTHDQKEALSLADRIAILHKGKFEQVSDPKTLYEYPKTKWVAQFVGEFPMNFLP 242
             TFI+VTHDQ EALS++DR+A+ + G+ EQV  P+ LY  P+T +VA FVG    N   
Sbjct: 185 GITFIFVTHDQGEALSMSDRVAVFNNGRIEQVDSPRDLYMRPRTPFVAGFVG--TSNVFD 242

Query: 243 GELMKEK----AQEIGFRPEWVEV---GKGNLSCMVESVEASGESRYLICNFKNNNITIL 295
           G LM EK          RPE + +   G+   +  +++V+  G +             ++
Sbjct: 243 G-LMAEKLCGMTGSFALRPEHIRLNTPGELQANGTIQAVQYQGAATRFELKLNGGEKLLV 301

Query: 296 SQ 297
           SQ
Sbjct: 302 SQ 303


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: 271
Number of extensions: 9
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: 337
Length adjustment: 28
Effective length of query: 296
Effective length of database: 309
Effective search space:    91464
Effective search space used:    91464
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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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