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_110806514.1 C8J30_RS14100 ABC transporter permease

Query= SwissProt::Q9F9B1
         (360 letters)



>NCBI__GCF_003217355.1:WP_110806514.1
          Length = 339

 Score =  148 bits (374), Expect = 2e-40
 Identities = 99/321 (30%), Positives = 159/321 (49%), Gaps = 30/321 (9%)

Query: 52  LIVLVLSLIAFGVILGGKFF--SAFTMTLILQQVAIVGIVGAAQTLVILTAGIDLSVGAI 109
           L+ + L     G I  G+ F  S   + +++ QV+++GI+    T VI+  GIDLS G+ 
Sbjct: 28  LVGIALVFEILGWIFQGQSFLMSIDRLKIMILQVSVIGIISVGVTQVIIAGGIDLSSGS- 86

Query: 110 MVLSSVIMGQFTFRY-------------GFPPALSVICGLGVGALCGYINGTLVARMKLP 156
            V+ +V M   +F                 P  + +  GL  GAL G ING L+A  K+P
Sbjct: 87  -VVGAVAMFAMSFAQVSTYARAVYPDLTDLPAIVPIALGLMAGALVGLINGALIAYAKIP 145

Query: 157 PFIVTLGMWQIVLASNFLYSANETIRAQDISANASILQFFGQNFRIGNAVFTYGVVVMVL 216
           PFI TLG   +V A  F   A    + Q IS       F G+            V + + 
Sbjct: 146 PFIATLGT--MVTARGF---AKWYTKGQPISFPTDDFAFIGKGMM--------PVAIFLA 192

Query: 217 LVCLLWYVLNRTAWGRYVYAVGDDPEAAKLAGVNVTRMLISIYTLSGLICALAGWALIGR 276
           +  +    +  T +G++ YA+G + +AA+++G+NV   LI +Y ++  + ALAG  +  R
Sbjct: 193 VAAIFHVAMKYTRYGKFTYAIGANQQAARVSGINVEHHLIKVYVVAATLAALAGMVVAAR 252

Query: 277 IGSVSPTAGQFANIESITAVVIGGISLFGGRGSIMGMLFGALIVGVFSLGLRLMGTDPQW 336
             +     G    +++I   VIGG+SL GGRGSI+G + G +I GV   G   +  D  +
Sbjct: 253 GQTAQAGMGLAYELDAIAMAVIGGVSLTGGRGSILGTMIGMVIFGVIISGFTFLRLDAYY 312

Query: 337 TYLLIGLLIIIAVAIDQWIRK 357
             ++ G++I+ AV  D + +K
Sbjct: 313 QEMIKGVIIVAAVVADVYRQK 333


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: 321
Number of extensions: 15
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: 360
Length of database: 339
Length adjustment: 29
Effective length of query: 331
Effective length of database: 310
Effective search space:   102610
Effective search space used:   102610
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 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