GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Phaeobacter inhibens BS107

Align Fructose import permease protein FrcC (characterized)
to candidate GFF2762 PGA1_c28050 putative sugar transport system, permease protein

Query= SwissProt::Q9F9B1
         (360 letters)



>FitnessBrowser__Phaeo:GFF2762
          Length = 353

 Score =  514 bits (1323), Expect = e-150
 Identities = 258/348 (74%), Positives = 295/348 (84%)

Query: 12  QEFEKVLADSSTDVASFDAHDKTLLQKLQHFLHSSPAAVPLIVLVLSLIAFGVILGGKFF 71
           Q +E   + S   VA FD  + + + + QH LH +P+ VPLIVLVLS+I FG++LG KFF
Sbjct: 5   QSYEAAASGSPEAVADFDQGETSFISRFQHMLHVTPSLVPLIVLVLSVIVFGLLLGSKFF 64

Query: 72  SAFTMTLILQQVAIVGIVGAAQTLVILTAGIDLSVGAIMVLSSVIMGQFTFRYGFPPALS 131
           S F +TLILQQV IVGIV  AQ+LVILTAGIDLSVGAIMVLSSV+MGQFTFRYG PP ++
Sbjct: 65  SPFALTLILQQVGIVGIVACAQSLVILTAGIDLSVGAIMVLSSVVMGQFTFRYGLPPEVA 124

Query: 132 VICGLGVGALCGYINGTLVARMKLPPFIVTLGMWQIVLASNFLYSANETIRAQDISANAS 191
           V CGL  G +CG+ING LVARMKLPPFIVTLGMWQIVLASNFLYSANETIR+Q I+A A 
Sbjct: 125 VACGLICGTICGFINGWLVARMKLPPFIVTLGMWQIVLASNFLYSANETIRSQTIAAEAP 184

Query: 192 ILQFFGQNFRIGNAVFTYGVVVMVLLVCLLWYVLNRTAWGRYVYAVGDDPEAAKLAGVNV 251
           +LQ FG+  +IG AVFTYGV+ MV+LV LL YVL  TAWGR+VYAVGDDPEAA+L+GV V
Sbjct: 185 LLQLFGEKIKIGGAVFTYGVIFMVILVVLLAYVLRHTAWGRHVYAVGDDPEAAELSGVKV 244

Query: 252 TRMLISIYTLSGLICALAGWALIGRIGSVSPTAGQFANIESITAVVIGGISLFGGRGSIM 311
           TR+LIS+Y LSGLICA AGWA+IGRIGSVSPT+GQ ANIESITAVVIGGISLFGGRGSI+
Sbjct: 245 TRVLISVYMLSGLICAFAGWAMIGRIGSVSPTSGQLANIESITAVVIGGISLFGGRGSIL 304

Query: 312 GMLFGALIVGVFSLGLRLMGTDPQWTYLLIGLLIIIAVAIDQWIRKVA 359
           G  FGALIVGVF+LGLRL+G D QWTYLLIGLLII AVA+DQWIRKV+
Sbjct: 305 GTFFGALIVGVFTLGLRLLGADAQWTYLLIGLLIIAAVAVDQWIRKVS 352


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: 540
Number of extensions: 17
Number of successful extensions: 1
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: 353
Length adjustment: 29
Effective length of query: 331
Effective length of database: 324
Effective search space:   107244
Effective search space used:   107244
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