Aligments for a candidate for deh in Escherichia coli BW25113

GapMind for catabolism of small carbon sources

Aligments for a candidate for deh in Escherichia coli BW25113

Align Acetate/monochloroacetate permease, Deh4p, of 468 aas and 12 TMSs (characterized)
to candidate 18139 b4111 proline/glycine betaine transporter (NCBI)

Query= TCDB::M1Q159
         (468 letters)



>lcl|FitnessBrowser__Keio:18139 b4111 proline/glycine betaine
           transporter (NCBI)
          Length = 500

 Score =  234 bits (598), Expect = 4e-66
 Identities = 147/458 (32%), Positives = 241/458 (52%), Gaps = 34/458 (7%)

Query: 15  KVIFASSAGTVIEWYDFYIFGALATTLASKFYNTGTPIGDIIAWLGTFAVGFLVRPFGAI 74
           K I A+S G  +EW+DF ++G +A  L   F+    P   ++A L TF+V FL+RP G +
Sbjct: 25  KAITAASLGNAMEWFDFGVYGFVAYALGKVFFPGADPSVQMVAALATFSVPFLIRPLGGL 84

Query: 75  VFGRIGDLVGRKFTYLITITIMGSCTFLIGLLPTQDVLGAWAGIILITMRILQGLALGGQ 134
            FG +GD  GR+    ITI IM   TF IGL+P+ D +G WA I+L+  ++ QG ++GG+
Sbjct: 85  FFGMLGDKYGRQKILAITIVIMSISTFCIGLIPSYDTIGIWAPILLLICKMAQGFSVGGE 144

Query: 135 YGGAATFVAEHAPQGKRGFYTSWIQTTATFGLLISLGVILITRISLGEADFNEWGWRLPF 194
           Y GA+ FVAE++P  KRGF  SW+   +  G ++  GV+++    +GEA+F +WGWR+PF
Sbjct: 145 YTGASIFVAEYSPDRKRGFMGSWLDFGSIAGFVLGAGVVVLISTIVGEANFLDWGWRIPF 204

Query: 195 MASILLVILSLWIRRALKESPLFQQ------LKDTKAVSKNPLKESFANPYNLRW-VLIA 247
             ++ L I+ L++R AL+E+P FQQ        D + +   P K SF       W  L+ 
Sbjct: 205 FIALPLGIIGLYLRHALEETPAFQQHVDKLEQGDREGLQDGP-KVSFKEIATKYWRSLLT 263

Query: 248 LFGATMGQGVVWYTGQFYALFYLQKIFNTPLIDSNLIVGAALLLSMPFF-VFFGSLSDRI 306
             G  +   V +Y    Y   YL    +    D  +++  A+++ M F     G LSDR 
Sbjct: 264 CIGLVIATNVTYYMLLTYMPSYLSHNLHYS-EDHGVLIIIAIMIGMLFVQPVMGLLSDRF 322

Query: 307 GRKKVMLSGMLLAVLTYYPIYGLMAAFAPTDPGQHFLFAYIGYNPVILGLL---VFIQVI 363
           GR+  +L G +   +   P                   A+I  N  ++GL+   + +  +
Sbjct: 323 GRRPFVLLGSVALFVLAIP-------------------AFILINSNVIGLIFAGLLMLAV 363

Query: 364 YVTMVYGPIAAFLVELFPTKIRYTSMSLPYHIGNGVFGGLVPMIGLILINATGNDFAGLW 423
            +    G +A+ L  +FPT IRY++++  ++I + +  GL P +   L+ ++ N     +
Sbjct: 364 ILNCFTGVMASTLPAMFPTHIRYSALAAAFNI-SVLVAGLTPTLAAWLVESSQNLMMPAY 422

Query: 424 WPMAIAGICLVVGFLLIKETNKVDISDASTSISVKHEA 461
           + M +A + L+ G + +KET    +  A+ + S   EA
Sbjct: 423 YLMVVAVVGLITG-VTMKETANRPLKGATPAASDIQEA 459


Lambda     K      H
   0.328    0.144    0.450 

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: 701
Number of extensions: 48
Number of successful extensions: 4
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: 468
Length of database: 500
Length adjustment: 34
Effective length of query: 434
Effective length of database: 466
Effective search space:   202244
Effective search space used:   202244
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 (21.7 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 paper from 2022 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

GapMind for catabolism of small carbon sources