GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1747 in Dechlorosoma suillum PS

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 Dsui_2237 Dsui_2237 ABC-type dipeptide/oligopeptide/nickel transport system, permease component

Query= TCDB::Q9X269
         (341 letters)



>FitnessBrowser__PS:Dsui_2237
          Length = 322

 Score =  162 bits (409), Expect = 1e-44
 Identities = 107/331 (32%), Positives = 168/331 (50%), Gaps = 29/331 (8%)

Query: 25  LKFLLKRLLTIAISMVVVIVITYVLMWLAPGNFFELQRVRDAIARVTTPDDPAYQATLKG 84
           + F+L+RLL  A  ++ V  + +  +++  GN  EL         V    DPA  A    
Sbjct: 1   MTFILRRLLHGAWVLLAVSALVFAALYVV-GNPVELL--------VDPQADPADTARTIA 51

Query: 85  FEERYGLNNPLWKQILMYLKGAVVFKFGPSFSDPARNIEDLIKEKFPITFTLALSSILFA 144
                GL+ PLW+Q L +L  A     G SF      +  LI E+ P T  LA S++  A
Sbjct: 52  ---ALGLDQPLWRQYLTFLGNAARGDLGTSFIHGVPALS-LILERLPATLELAASALFLA 107

Query: 145 LVVGVPLGILAALKKNTWIDYTAMTVSVIGVAIPSYVVAVFLILIFSIYLGWLPTSG--- 201
           L++G+PLG+ A L+  +         S +G A+P++ V + LIL+F++ L WLP  G   
Sbjct: 108 LLLGIPLGLWAGLRPTSLAGRLIGAASTLGFALPAFWVGLMLILVFAVQLQWLPPGGRGE 167

Query: 202 -------------WEGIRTKILPTIALALGPLASVARFTRVSLLDTLNQDFIRTAYAKGG 248
                         +G R  +LP + LAL   A V R  R    + L QD++R A AKG 
Sbjct: 168 TREVLGLSLSVFTLDGWRHLLLPALNLALYKAALVVRLVRAGSREALAQDYVRFARAKGL 227

Query: 249 DDRTVIMKHALRPSMIPLVTIVGPQMAYLMVGTVWVENIFRIPGLGQLFANAAVTRDYPL 308
            +  V+  H L  ++IP+VT++G ++  L+   V  E +F  PG+G+L  +A    D P+
Sbjct: 228 TESRVVTGHVLPNTLIPVVTVLGMELGALIAFAVVTETVFGWPGMGKLLMDAINALDRPV 287

Query: 309 LVTSTFILALTVMIMNLIVDVLYAILDPRIK 339
           +V      A   +++NL+V++LY  LDPR++
Sbjct: 288 VVAYLLFAAALFVVLNLLVELLYGWLDPRVR 318


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: 289
Number of extensions: 12
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: 341
Length of database: 322
Length adjustment: 28
Effective length of query: 313
Effective length of database: 294
Effective search space:    92022
Effective search space used:    92022
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