GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruF in Rhizobium leguminosarum bv. trifolii WSM1325

Align Fructose import permease protein FruF (characterized)
to candidate WP_003562293.1 RLEG_RS23605 ABC transporter permease

Query= SwissProt::Q8G846
         (356 letters)



>NCBI__GCF_000023185.1:WP_003562293.1
          Length = 354

 Score =  161 bits (408), Expect = 2e-44
 Identities = 103/343 (30%), Positives = 179/343 (52%), Gaps = 29/343 (8%)

Query: 24  SIVAFILLVIICTIFQHDFLALSWNSNTGGLAGPLITMLQESARYLMIATGMTLVISTAG 83
           + +A   ++I   IF  +F + +           +I M +  A    +A GMT VI T G
Sbjct: 27  TFIALFAVIIFFAIFAPNFTSTA----------NMILMSKHVALNAFLAMGMTFVIITGG 76

Query: 84  IDLSVGSVMAVAGAAAMQTLSNGM----------NVWLSILIALAVGLAIGCVNGALVSF 133
           IDLSVGS++ + G  A   +  G+          N++  +LI +++GL IG +NG L++ 
Sbjct: 77  IDLSVGSIVGLCGMVAGGLILYGIELPIGYTIFFNLFEIVLITVSIGLLIGLINGLLITK 136

Query: 134 LGLQPFITTLIMMLAGRGMAKVITSGE---NTDASAVAGNEPLKWFANGFILGIPANFVI 190
           L + PFI TL  +   RG+A + + G+   N             +F  G ILG+P +  I
Sbjct: 137 LNVAPFIATLGTLYIARGLALLSSDGQTFPNLVGRPEYATTGFDFFGAGRILGLPVSIWI 196

Query: 191 AVIIVILVGLLCRKTAMGMMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAAIAGLFA 250
            +++ +L   + R T +G  I AVG N+ A+RM+GI+   +   VY  SG  AAI G+  
Sbjct: 197 LIVLALLAAYVARSTPIGRHIFAVGGNERAARMSGIRVDVVKIFVYMFSGLCAAIVGVVI 256

Query: 251 TASVMRVDVVKTGQDLEMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKTIITLGV 310
           ++ +M      TG+  E+ AI A V+GGTS+ GG+ ++ G+ +GA +I ++   ++ +GV
Sbjct: 257 SSELMAAHPA-TGESFELNAIAAAVLGGTSMSGGRGTIGGTIIGAFVIGILSDGLVMMGV 315

Query: 311 NAEATPAFFAVVVIVICVMQAPKIHNLSANMKRKRALKAQAKA 353
           +     +F+ +V+  + ++ A  +      ++++  L   AKA
Sbjct: 316 S-----SFWQMVIKGLVIIIAVVVDQAQRRLQQRVTLMQMAKA 353


Lambda     K      H
   0.325    0.136    0.384 

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: 310
Number of extensions: 17
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: 356
Length of database: 354
Length adjustment: 29
Effective length of query: 327
Effective length of database: 325
Effective search space:   106275
Effective search space used:   106275
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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