GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1748 in Pedobacter sp. GW460-11-11-14-LB5

Align TM1748, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate CA265_RS18010 CA265_RS18010 peptide transporter

Query= TCDB::Q9X270
         (289 letters)



>FitnessBrowser__Pedo557:CA265_RS18010
          Length = 380

 Score =  192 bits (488), Expect = 1e-53
 Identities = 98/222 (44%), Positives = 146/222 (65%), Gaps = 1/222 (0%)

Query: 67  FIFGTDALGRDLFSRILYSLRNACIIGFGSQFVVLIIGGILGAVAGFKGGWIDKFIMSIV 126
           +I GTD  GRDL SR++  +R +  +G  +  + L IG  LGA+AG+ GG +D  I   +
Sbjct: 155 YILGTDIYGRDLLSRLILGIRVSLSVGLMAVLISLFIGVSLGAIAGYFGGRVDAAISWFM 214

Query: 127 DIMFAFPTFLFNVILVTALGRGLFTIFLAIGLTGWAGMARLVRGQVLYLKNSEFVEAAKA 186
           +++++ P+ L  + +  ALG+G + IF+A+GL+ W  +ARLVRGQV+ LK  EFVEAA+A
Sbjct: 215 NVVWSLPSLLLVIAISFALGKGFWQIFIAVGLSTWVDVARLVRGQVMALKEVEFVEAARA 274

Query: 187 AGASTFYIIRKHILPNMIGPILVNLAFGVPGAMMTESGLAVIGMGVRPPMPSWGNLIGEG 246
            G ST   I KHILPN+ GPILV  +     A++ E+GL+ +G G +PPMPSWG++I E 
Sbjct: 275 LGFSTSRTIIKHILPNIAGPILVVASSNFASAILLETGLSFLGFGAQPPMPSWGSMIKEH 334

Query: 247 IG-MMMAFPHLLIFPAVTFAFTLISFTFLADGLRDAFNPRSE 287
            G ++M   +L + P +   FT+ +F  LA GLRDAF+ + +
Sbjct: 335 YGYIIMDAAYLAVLPGLAIMFTVYAFNVLAIGLRDAFDVKGQ 376



 Score = 37.4 bits (85), Expect = 5e-07
 Identities = 17/35 (48%), Positives = 23/35 (65%)

Query: 14 KAFWLRFKKNKMAVIGGVFVLILIALAILAPYIAP 48
          K  WL+FK+NK A  G VF+L+L+ + IL   I P
Sbjct: 7  KKVWLKFKRNKFAFGGLVFILLLMVMGILGYLIMP 41


Lambda     K      H
   0.331    0.147    0.457 

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: 301
Number of extensions: 17
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 289
Length of database: 380
Length adjustment: 28
Effective length of query: 261
Effective length of database: 352
Effective search space:    91872
Effective search space used:    91872
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.2 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.

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 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