GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Escherichia coli BW25113

Align MglC aka B2148, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate 17810 b3750 ribose ABC transporter permease protein (NCBI)

Query= TCDB::P23200
         (336 letters)



>FitnessBrowser__Keio:17810
          Length = 321

 Score =  193 bits (491), Expect = 4e-54
 Identities = 116/323 (35%), Positives = 183/323 (56%), Gaps = 21/323 (6%)

Query: 12  YLKEGGIYVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLS 71
           +L E    + LLVL+AI+    P F ++ NL NIL Q+SV  I+A+G+  +I+T G DLS
Sbjct: 16  WLMEQKSLIALLVLIAIVSTLSPNFFTINNLFNILQQTSVNAIMAVGMTLVILTSGIDLS 75

Query: 72  AGRQVGLAAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLN 131
            G  + L   VAA+++    NA             + +    A+GA IG + G+I+A   
Sbjct: 76  VGSLLALTGAVAASIVGIEVNA------------LVAVAAALALGAAIGAVTGVIVAKGR 123

Query: 132 VTPFITTLGTMIIVYGINSLYYDFVGASPISGFDSGFSTFAQGFVALGSFR-LSYITFYA 190
           V  FI TL  M+++ G+  +Y      SP++   +GF+  A  F   G  R L   T   
Sbjct: 124 VQAFIATLVMMLLLRGVTMVY---TNGSPVN---TGFTENADLFGWFGIGRPLGVPTPVW 177

Query: 191 LIAVAFV--WVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGML 248
           ++ + F+  W + + TR G+ I+A+GGN  A ++SG+NV    +++Y+L G+  +  G++
Sbjct: 178 IMGIVFLAAWYMLHHTRLGRYIYALGGNEAATRLSGINVNKIKIIVYSLCGLLASLAGII 237

Query: 249 EAGRIGSATNNLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGV 308
           E  R+ SA    G  YELDAIAA V+GG S +GG G ++G + G +I   +N GL  +GV
Sbjct: 238 EVARLSSAQPTAGTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGV 297

Query: 309 NPYWQYIIKGAIIIFAVALDSLK 331
           + Y+Q I+K  +I+ AV +D+ K
Sbjct: 298 SSYYQMIVKAVVILLAVLVDNKK 320


Lambda     K      H
   0.327    0.143    0.415 

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: 296
Number of extensions: 22
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: 336
Length of database: 321
Length adjustment: 28
Effective length of query: 308
Effective length of database: 293
Effective search space:    90244
Effective search space used:    90244
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: 49 (23.5 bits)

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

Links

Downloads

Related tools

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