GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1748 in Marivita geojedonensis DPG-138

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 WP_085636091.1 MGEO_RS07450 dipeptide/oligopeptide/nickel ABC transporter permease/ATP-binding protein

Query= TCDB::Q9X270
         (289 letters)



>NCBI__GCF_002115805.1:WP_085636091.1
          Length = 628

 Score =  165 bits (417), Expect = 3e-45
 Identities = 86/271 (31%), Positives = 151/271 (55%), Gaps = 1/271 (0%)

Query: 16  FWLRFKKNKMAVIGGVFVLILIALAILAPYIAPYPYDEPHYIRAFEGP-SKDFIFGTDAL 74
           F+    +N++A+ G + + +++ LA+L P +     D  +    F+ P S+  + GTD L
Sbjct: 4   FFRLLARNRLALAGLIVMGLVVLLALLTPLLPLADPDVTNTANRFKPPLSEGALLGTDHL 63

Query: 75  GRDLFSRILYSLRNACIIGFGSQFVVLIIGGILGAVAGFKGGWIDKFIMSIVDIMFAFPT 134
           GRDL SR+++  R +  +GF +  +   +G  +G +AGF GG  D  IM  VD++ AFP 
Sbjct: 64  GRDLLSRLMWGTRLSLAVGFAAAVIAATLGAAIGIIAGFYGGRTDNVIMRGVDMLMAFPY 123

Query: 135 FLFNVILVTALGRGLFTIFLAIGLTGWAGMARLVRGQVLYLKNSEFVEAAKAAGASTFYI 194
            L  + +V ALG GL    +A+        AR +RG  + + + EFV+AA+ +G +   I
Sbjct: 124 ILLALAIVAALGPGLMNALIAVAAVNIPFFARNIRGITVGIAHKEFVDAARLSGMTDARI 183

Query: 195 IRKHILPNMIGPILVNLAFGVPGAMMTESGLAVIGMGVRPPMPSWGNLIGEGIGMMMAFP 254
           I   +LPN++  I++ ++  V   ++  +GL+ +G+G +PP    G+++GE    ++  P
Sbjct: 184 IATEVLPNVVPVIVIAMSTTVGWMILETAGLSFLGLGSQPPQADLGSMLGEARSALITNP 243

Query: 255 HLLIFPAVTFAFTLISFTFLADGLRDAFNPR 285
           H  + P V     +++   L DG+RDA +PR
Sbjct: 244 HTSVVPGVMILIIVMAINLLGDGVRDALDPR 274


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: 352
Number of extensions: 15
Number of successful extensions: 2
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: 628
Length adjustment: 32
Effective length of query: 257
Effective length of database: 596
Effective search space:   153172
Effective search space used:   153172
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 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