GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Shewanella sp. ANA-3

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate 7026098 Shewana3_3240 transport system permease protein (RefSeq)

Query= SwissProt::P15030
         (332 letters)



>FitnessBrowser__ANA3:7026098
          Length = 338

 Score =  161 bits (407), Expect = 2e-44
 Identities = 111/322 (34%), Positives = 170/322 (52%), Gaps = 10/322 (3%)

Query: 15  VAALIIIFWLSLFCYSAIPVSGADATRALLP-------GHTPTLPEALVQNLRLPRSLVA 67
           +A L+I+  L       + +S  D+  A+         G+     + +V N+RLPR+L+A
Sbjct: 11  MATLLILSSLLSVSVGPVNISLIDSLSAVFNWATEQNIGNLAPHEQLVVSNVRLPRTLLA 70

Query: 68  VLIGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALSPTPIAGYSLSFIAAC 127
           + +GA LA  G ++Q L  NP+A P ++G++SGAAL  A+     P       +S  A  
Sbjct: 71  LAVGAMLAQCGAVMQGLFRNPLADPGIIGVSSGAALGAAICIVQFPHA-ESVMISVSAFS 129

Query: 128 GGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDHAY-GIFYWLA 186
            G ++ L+V         T     L+L+G+A++A       +   LA D A   +  W  
Sbjct: 130 SGLITTLIVYRLASSALGT-SVVLLLLSGVAVAALAGAGIGVLTYLANDMALRDLTLWQM 188

Query: 187 GGVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLVINMLV 246
           G ++ A+WQ V   L V+          A  LN L L ++ A  LG+++  L+L + +L 
Sbjct: 189 GSIAGAQWQYVGLCLVVLALLSWQFNRDAKALNALLLGEAEARHLGIDVDSLKLRLILLC 248

Query: 247 LLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLARALAF 306
            L VG  V+  G + FIGL+VPHL R   G D + +LP+S LLGA L+ LAD+ ARA   
Sbjct: 249 ALGVGVSVAATGIIGFIGLVVPHLVRMLLGPDHQRLLPMSALLGAALLALADIGARAFLP 308

Query: 307 PGDLPAGAVLALIGSPCFVWLV 328
           P +LP G V ALIG+P F++L+
Sbjct: 309 PAELPVGLVTALIGAPFFIFLL 330


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: 281
Number of extensions: 11
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: 332
Length of database: 338
Length adjustment: 28
Effective length of query: 304
Effective length of database: 310
Effective search space:    94240
Effective search space used:    94240
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