GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Escherichia coli BW25113

Align TM0030, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate 15607 b1486 D-ala-D-ala transporter subunit (NCBI)

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__Keio:15607
          Length = 340

 Score =  157 bits (397), Expect = 4e-43
 Identities = 112/345 (32%), Positives = 176/345 (51%), Gaps = 26/345 (7%)

Query: 7   FKYLLRRFIFLLVTYIVATTIV-FILPRAIPGNPLSQILSGLSRVAQANPEAIRAAERTL 65
           F  +LR+  + LV  +    ++ FI+   IPG+P +++L+G  R + A  E IR      
Sbjct: 3   FWSILRQRCWGLVLVVAGVCVITFIISHLIPGDP-ARLLAG-DRASDAIVENIR------ 54

Query: 66  MEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAW 125
            ++ GL +P YVQ++ +++    GDLGTSI    R V++ +    P TL L   A ++A 
Sbjct: 55  -QQLGLDQPLYVQFYRYVSDLFHGDLGTSIRT-GRPVLEELRIFFPATLELAFGALLLAL 112

Query: 126 ILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLP------- 178
           ++G  LG L+A  RN W+D  V   ++     P +WLG+  I LF   L  LP       
Sbjct: 113 LIGIPLGILSAVWRNRWLDHLVRIMAITGISTPAFWLGLGVIVLFYGHLQILPGGGRLDD 172

Query: 179 -------VQGAYSQGTIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIYELG 231
                  V G Y    +   +   F + L+H I+P  ++    +G  A  +R  ++ +L 
Sbjct: 173 WLDPPTHVTGFYLLDALLEGNGEVFFNALQHLILPALTLAFVHLGIVARQIRSAMLEQLS 232

Query: 232 SDYAMFSEYLGMKDKRIFK-YVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYL 290
            DY   +   G+    I   Y   N+L+P IT L L+LG +L GA++TE VF +PG G  
Sbjct: 233 EDYIRTARASGLPGWYIVLCYALPNALIPSITVLGLALGDLLYGAVLTETVFAWPGMGAW 292

Query: 291 LFRALTTLDYPLIQGIFVILIASIYLANFIVDFLYALIDPRIRLG 335
           +  ++  LD+P + G  V++  +  L N +VD LY  IDPRI  G
Sbjct: 293 VVTSIQALDFPAVMGFAVVVSFAYVLVNLVVDLLYLWIDPRIGRG 337


Lambda     K      H
   0.329    0.146    0.449 

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: 337
Number of extensions: 20
Number of successful extensions: 5
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: 338
Length of database: 340
Length adjustment: 28
Effective length of query: 310
Effective length of database: 312
Effective search space:    96720
Effective search space used:    96720
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 (21.8 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