GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1747 in Dinoroseobacter shibae DFL-12

Align TM1747, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate 3610412 Dshi_3793 binding-protein-dependent transport systems inner membrane component (RefSeq)

Query= TCDB::Q9X269
         (341 letters)



>FitnessBrowser__Dino:3610412
          Length = 317

 Score =  157 bits (396), Expect = 4e-43
 Identities = 100/328 (30%), Positives = 169/328 (51%), Gaps = 27/328 (8%)

Query: 25  LKFLLKRLLTIAISMVVVIVITYVLMWLAPGNFFELQRVRDAIARVTTPDDPA-YQATLK 83
           L FL++R+      M+ V ++ + L+ ++PG         D +  +  PD     Q  L 
Sbjct: 2   LTFLIRRVAYTIPIMLGVSLVCFALVHISPG---------DPLVSILPPDASVELQQQLM 52

Query: 84  GFEERYGLNNPLWKQILMYLKGAVVFKFGPSFSDPARNIEDLIKEKFPITFTLALSSILF 143
                YG +    +Q + +L  AV    G S +   R +   +      T  LA+++ + 
Sbjct: 53  AI---YGFDRSYPEQFIRWLGRAVQGDLGNSIAT-GRPVTAEVLNAVGNTLILAVTATII 108

Query: 144 ALVVGVPLGILAALKKNTWIDYTAMTVSVIGVAIPSYVVAVFLILIFSIYLGWLPTSG-- 201
               G   G +A   +++WID  A T+SV+GV+IP Y + + L++IFS+ LGWLP +G  
Sbjct: 109 GFTFGGLFGFVAGYFRDSWIDKLASTISVVGVSIPHYWLGMVLVIIFSVQLGWLPATGAG 168

Query: 202 ----------WEGIRTKILPTIALALGPLASVARFTRVSLLDTLNQDFIRTAYAKGGDDR 251
                     WE ++  ILP + +++ P+  VAR  R  + D L Q+++    AKG  DR
Sbjct: 169 PRGSSEWAFDWEHLQYLILPAVTMSVIPMGIVARTVRALVADILQQEYVTGLRAKGLLDR 228

Query: 252 TVIMKHALRPSMIPLVTIVGPQMAYLMVGTVWVENIFRIPGLGQLFANAAVTRDYPLLVT 311
            V+  H ++ +    + ++G Q+ YL+ G++ +E +F  PG G L   A   RD PLL  
Sbjct: 229 GVLA-HVIKNAAPTALAVMGLQLGYLLGGSILIETVFSWPGTGFLLGQAIFQRDLPLLQG 287

Query: 312 STFILALTVMIMNLIVDVLYAILDPRIK 339
           +  +LA+  +I+NL+VDV  + LDPR++
Sbjct: 288 TILVLAMFFVILNLLVDVAQSALDPRLQ 315


Lambda     K      H
   0.328    0.143    0.429 

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: 272
Number of extensions: 14
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: 341
Length of database: 317
Length adjustment: 28
Effective length of query: 313
Effective length of database: 289
Effective search space:    90457
Effective search space used:    90457
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.

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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