GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Rhodobacter viridis JA737

Align Fructose import permease protein FrcC (characterized)
to candidate WP_110806371.1 C8J30_RS13480 sugar ABC transporter permease

Query= SwissProt::Q9F9B1
         (360 letters)



>NCBI__GCF_003217355.1:WP_110806371.1
          Length = 416

 Score =  134 bits (336), Expect = 6e-36
 Identities = 108/371 (29%), Positives = 163/371 (43%), Gaps = 61/371 (16%)

Query: 47  PAAVPLIVLVLSLIAFGVILGGKFFSAFTMTLILQQVAIVGIVGAAQTLVILTAGIDLSV 106
           P  V LI++ L   A   +    F     +  +L   A VG +     +V+L   IDLSV
Sbjct: 45  PVVVGLILISLVFTALNPV----FLLPNNLVNLLFDAAAVGFISLGIVMVLLLGEIDLSV 100

Query: 107 GAIMVLSSVIMGQFTFRYGFPPALSVICGLGVGALCGYINGTLVARMKLPPFIVT----- 161
           G++  L+S ++G      G P  L+++  L  GA+ G    TL+ R  +P F+ T     
Sbjct: 101 GSMSGLASALVGVLWVNMGLPLPLALLAALSAGAMMGAAYATLLNRFTMPSFVSTLSGLL 160

Query: 162 --LGMWQIVLA---------SNFLYSANETIRAQDISANA-------SILQFFGQNFRI- 202
             LGM   +L          ++FL    + +   D ++ A        IL F  +  +  
Sbjct: 161 ALLGMQLYILGPTGSINLPYASFLVRFGQILIMPDWASYALALVPGLGILWFGFRQMKAR 220

Query: 203 --GNAVFT------------------------------YGVVVMVLLVCLLWYVLNRTAW 230
              N  +T                              +  VV VL V  + Y L RT W
Sbjct: 221 AAANLSYTSASVVLVKAGAVTVALEGAVAYLNLGRGVPFMFVVFVLCVAAMQYALTRTKW 280

Query: 231 GRYVYAVGDDPEAAKLAGVNVTRMLISIYTLSGLICALAGWALIGRIGSVSPTAGQF-AN 289
           GR ++AVG + EAA+ +G+ V R+ ++ + L   + AL G     R+ + S  AG    N
Sbjct: 281 GRSMFAVGGNIEAARRSGIKVKRIRLTAFMLGSSLAALGGVFSAARLATASQQAGTGDVN 340

Query: 290 IESITAVVIGGISLFGGRGSIMGMLFGALIVGVFSLGLRLMGTDPQWTYLLIGLLIIIAV 349
           + +I A VIGG SLFGGRGS    L G L++   S GL L+       Y++ G ++ IAV
Sbjct: 341 LNAIAAAVIGGTSLFGGRGSAWAALLGVLVIQSISNGLTLLNLSSSLRYMITGAVLAIAV 400

Query: 350 AIDQWIRKVAA 360
            ID   R+  A
Sbjct: 401 IIDSLARQSRA 411


Lambda     K      H
   0.327    0.141    0.420 

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: 354
Number of extensions: 25
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 2
Length of query: 360
Length of database: 416
Length adjustment: 30
Effective length of query: 330
Effective length of database: 386
Effective search space:   127380
Effective search space used:   127380
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: 50 (23.9 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