GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Dinoroseobacter shibae DFL-12

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate 3607150 Dshi_0572 transport system permease protein (RefSeq)

Query= SwissProt::P15030
         (332 letters)



>FitnessBrowser__Dino:3607150
          Length = 360

 Score =  170 bits (430), Expect = 6e-47
 Identities = 112/327 (34%), Positives = 177/327 (54%), Gaps = 18/327 (5%)

Query: 23  WLSLFCYSA----IPVSGADATRALLPG-HTPTLP---EALVQNLRLPRSLVAVLIGASL 74
           W+ L   SA    I  +GA    A+     T TL    + ++ ++RLPR  + +L+GA+L
Sbjct: 31  WIFLLAVSAFSLGIGAAGAQVRAAVADWIRTGTLDAGAQVILFDIRLPRLALGLLVGAAL 90

Query: 75  ALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALSPT-------PIAGYSLSFIAAC 127
           A+AG ++Q L  NP+A P ++G+++GA L   L   L           +  Y +   A  
Sbjct: 91  AVAGAVMQGLFRNPLADPGIVGVSAGAGLGAILAIVLGAALPAFFIDALGNYLIPLAAFA 150

Query: 128 GGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDHAY-GIFYWLA 186
           GG  S +L+         T     ++LAGIAL+A    L+ I + +A+D     + +W  
Sbjct: 151 GGWGSTILLYKVSTRRGRTSVAT-MLLAGIALAALTGALSGILVYIADDRQLRDLTFWGL 209

Query: 187 GGVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLVINMLV 246
           G ++ A W  V    P++  A     LLA  LN + L ++ A  +GV L RL+    ++V
Sbjct: 210 GSLAGATWTKVLIAGPLIAVAFLSAPLLARGLNGMALGEAAAAHMGVALERLKTGAILIV 269

Query: 247 LLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLARALAF 306
               GA V+V+G + F+G++VPHL R   G D R +LP + LLGA+L++LAD ++R +  
Sbjct: 270 ASATGAAVAVSGGIGFVGIVVPHLLRIAVGPDHRTLLPNAALLGASLLVLADCISRTIIA 329

Query: 307 PGDLPAGAVLALIGSPCFVW-LVRRRG 332
           P +LP G V A++G+P F+W L+R RG
Sbjct: 330 PAELPIGIVTAVLGAPVFLWILLRARG 356


Lambda     K      H
   0.327    0.140    0.436 

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: 331
Number of extensions: 16
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: 332
Length of database: 360
Length adjustment: 29
Effective length of query: 303
Effective length of database: 331
Effective search space:   100293
Effective search space used:   100293
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