GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1748 in Acidovorax sp. GW101-3H11

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 Ac3H11_696 Dipeptide transport system permease protein DppC (TC 3.A.1.5.2)

Query= TCDB::Q9X270
         (289 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_696
          Length = 287

 Score =  155 bits (393), Expect = 8e-43
 Identities = 87/278 (31%), Positives = 149/278 (53%), Gaps = 8/278 (2%)

Query: 15  AFWLRFKK-------NKMAVIGGVFVLILIALAILAPYIAPYPYDEPHYIRAFEGPSKDF 67
           +FW R +         K+ +   + + ++ ++A++ P+++    +          PS   
Sbjct: 6   SFWHRLRAVLRRLFARKVVLASAIVITLVASIAVVFPWVSDADPNALSISERLHAPSGTH 65

Query: 68  IFGTDALGRDLFSRILYSLRNACIIGFGSQFVVLIIGGILGAVAGFKGGWIDKFIMSIVD 127
             GTD LGRD+  RI++  R + +IG  +    +++G +LG +AGF    +D  +M +VD
Sbjct: 66  WAGTDELGRDVLLRIVHGARYSLLIGLVTAAGAVLLGTLLGMLAGFFRR-LDAPLMRLVD 124

Query: 128 IMFAFPTFLFNVILVTALGRGLFTIFLAIGLTGWAGMARLVRGQVLYLKNSEFVEAAKAA 187
            M +FP  L  + LV+ LG  L+ + LA+ +     +AR+VR   L L+   FV+AA+A 
Sbjct: 125 AMMSFPDILLGIALVSILGVSLWNVMLALVIVYTPRVARVVRATTLVLRELLFVDAARAL 184

Query: 188 GASTFYIIRKHILPNMIGPILVNLAFGVPGAMMTESGLAVIGMGVRPPMPSWGNLIGEGI 247
           G  T  I+ +HILPN++ PILV + F    A++ E+GL+ +G+GV P +P+WG +I   +
Sbjct: 185 GVRTHLILWRHILPNLMSPILVQVTFIFAYAILAEAGLSFLGVGVPPDIPTWGTMIAGSL 244

Query: 248 GMMMAFPHLLIFPAVTFAFTLISFTFLADGLRDAFNPR 285
                    +  P V    T +S   L DG+RD  +P+
Sbjct: 245 DYADKAFWTIFAPGVAIVLTALSLQMLGDGVRDLLDPK 282


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: 212
Number of extensions: 10
Number of successful extensions: 3
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: 289
Length of database: 287
Length adjustment: 26
Effective length of query: 263
Effective length of database: 261
Effective search space:    68643
Effective search space used:    68643
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: 47 (22.7 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