GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Sinorhizobium meliloti 1021

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate SMc01511 SMc01511 hemin transport system permease transmembrane protein

Query= SwissProt::P15030
         (332 letters)



>FitnessBrowser__Smeli:SMc01511
          Length = 366

 Score =  181 bits (458), Expect = 3e-50
 Identities = 102/287 (35%), Positives = 166/287 (57%), Gaps = 15/287 (5%)

Query: 55  LVQNLRLPRSLVAVLIGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALSPT 114
           ++ ++RLPR+++ +L+GASLA++G ++Q L  NP+A P L+G++SGA+L   L   L   
Sbjct: 77  IILDIRLPRAVLGMLVGASLAVSGVVMQGLFRNPLADPGLVGVSSGASLGAVLLIVLGDV 136

Query: 115 PIAG-------YSLSFIAACGGGVSWLL---VMTAGGGFRHTHDRNKLILAGIALSAFCM 164
                      Y+L F A  GG  + LL   + T GG          ++LAGIAL A   
Sbjct: 137 AFGPLFAVFGFYALPFGAFLGGLATTLLLYRIATRGGQTSVA----TMLLAGIALGALAG 192

Query: 165 GLTRITLLLAEDHAY-GIFYWLAGGVSHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNL 223
            +T + + +A+D     + +W  G ++ A W  +    P+++ ++ VV  LA  LN + L
Sbjct: 193 AVTGVLVFIADDKQLRDLTFWGLGSLAGANWTKIAAAGPIILVSLAVVPFLARGLNAITL 252

Query: 224 SDSTAHTLGVNLTRLRLVINMLVLLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVL 283
            ++ A+ +GV + RL+ +    V    GA V+V+G + F+G++VPHL R   G D R +L
Sbjct: 253 GEAAAYHMGVPVQRLKNIAVFSVAGATGASVAVSGGIGFVGIVVPHLLRLVIGPDHRYLL 312

Query: 284 PVSMLLGATLMLLADVLARALAFPGDLPAGAVLALIGSPCFVWLVRR 330
           P S LLG TL++ AD+LAR +  P +LP G + A +G+P F+W++ R
Sbjct: 313 PASALLGGTLLIFADMLARTIVSPAELPIGIITAFVGAPFFLWVLLR 359



 Score = 23.9 bits (50), Expect = 0.007
 Identities = 13/42 (30%), Positives = 21/42 (50%)

Query: 151 KLILAGIALSAFCMGLTRITLLLAEDHAYGIFYWLAGGVSHA 192
           + ++A +A+ A    +T IT   A+     IF WL+G    A
Sbjct: 28  RCLIAVLAVLAAATFMTSITTGAADASLSSIFRWLSGETDQA 69


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: 329
Number of extensions: 21
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 332
Length of database: 366
Length adjustment: 29
Effective length of query: 303
Effective length of database: 337
Effective search space:   102111
Effective search space used:   102111
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