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_012757421.1 RLEG_RS09445 ABC transporter permease

Query= SwissProt::Q8G846
         (356 letters)



>NCBI__GCF_000023185.1:WP_012757421.1
          Length = 337

 Score =  243 bits (620), Expect = 5e-69
 Identities = 139/338 (41%), Positives = 214/338 (63%), Gaps = 6/338 (1%)

Query: 15  KLLSSNLTWSIVAFILLVIICTIFQHDFLALSWNSNTGGLAGPLITMLQESARYLMIATG 74
           K L+  L   ++A ++++++  I    F  +   ++   L G LI +L   A   ++A G
Sbjct: 6   KALAYRLAPQLIALVVILLLNFITSPQFFNVVVQNDR--LYGSLIDVLNRGAPVALLAIG 63

Query: 75  MTLVISTAGIDLSVGSVMAVAGAAAMQTLSNGMNVWLSILIALAVGLAIGCVNGALVSFL 134
           MTLVI+T GIDLSVG+V+A+ GA A  ++ +G +V  +I++ LA+GLA G  NG LV+ L
Sbjct: 64  MTLVIATKGIDLSVGAVIAICGAVAASSIVSGNSVAYTIILTLAIGLACGVWNGFLVAVL 123

Query: 135 GLQPFITTLIMMLAGRGMAKVITSGENTDASAVAGNEPLKWFANGFILGIPANFVIAVII 194
            +QP I TL++M+AGRG+A++IT G    A     N+ L +F +G +L +P   VI +++
Sbjct: 124 NIQPIIATLVLMVAGRGIAQLITEG----AILTFNNDGLTFFGSGSLLLLPMPVVIWLLV 179

Query: 195 VILVGLLCRKTAMGMMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAAIAGLFATASV 254
            +LV LL R+TA+GM+IEAVGIN+ AS ++GI+   +L  VY +SG  A+IAG+   A +
Sbjct: 180 GLLVILLVRRTALGMLIEAVGINRRASTLSGIQTPVLLMAVYMLSGLCASIAGIIVAADI 239

Query: 255 MRVDVVKTGQDLEMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKTIITLGVNAEA 314
              D    G  LE+ AILAVV+GG SLLGG+FS+ GS +GA+II  +   I++ G   E 
Sbjct: 240 KGADANNAGLWLELDAILAVVVGGNSLLGGRFSILGSLIGAMIIQAVNTGILSAGFPPEF 299

Query: 315 TPAFFAVVVIVICVMQAPKIHNLSANMKRKRALKAQAK 352
                AV++IVI V+Q+P + +L+    R++  + Q K
Sbjct: 300 NLIIKAVIIIVILVIQSPAVQSLAIFASRRQGGREQPK 337


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: 326
Number of extensions: 22
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: 356
Length of database: 337
Length adjustment: 29
Effective length of query: 327
Effective length of database: 308
Effective search space:   100716
Effective search space used:   100716
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