GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Pseudomonas putida KT2440

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate PP_4688 PP_4688 Heme/hemin ABC transporter, permease protein

Query= SwissProt::P15030
         (332 letters)



>FitnessBrowser__Putida:PP_4688
          Length = 345

 Score =  170 bits (431), Expect = 4e-47
 Identities = 114/286 (39%), Positives = 160/286 (55%), Gaps = 10/286 (3%)

Query: 53  EALVQNLRLPRSLVAVLIGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALS 112
           E ++  +RLPR+L+ + +GA LAL+G  +Q L  NP+A P L+G+ +GAA+  A+     
Sbjct: 59  EMILGQIRLPRTLLGLAVGAVLALSGVAMQGLFRNPLADPGLVGVAAGAAVGAAVAIVGG 118

Query: 113 ------PTPIAGYSLSFIAACGGGVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGL 166
                 P   A Y LSF A  GG     LV   G     T+    ++LAG+A++A     
Sbjct: 119 AWFGGMPDAFAPYLLSFCAFVGGLGVTALVYRLGRRDGQTNVAT-MLLAGVAMTALGGAA 177

Query: 167 TRITLLLAEDHAYG-IFYWLAGGVSHARWQDVWQLLPVVVTAVPVVL-LLANQLNLLNLS 224
             +   LA+D     + +W  G ++ A ++ +W LL +V T V V L   A  LN L L 
Sbjct: 178 VGLFSYLADDATLRTLTFWNLGSLNGASYERLWPLL-LVATGVAVWLPRRAKALNALLLG 236

Query: 225 DSTAHTLGVNLTRLRLVINMLVLLLVGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLP 284
           +S A  LGV++ RL+  +     L VGA V+ AG + FIGL+VPHL R  AG D R VLP
Sbjct: 237 ESEARHLGVDVERLKRELVFCTALGVGAAVAAAGLIGFIGLVVPHLVRLLAGPDHRVVLP 296

Query: 285 VSMLLGATLMLLADVLARALAFPGDLPAGAVLALIGSPCFVWLVRR 330
            S+L G  LML AD+ AR L  P +LP G V A IG+P F++L+ R
Sbjct: 297 ASLLAGGVLMLFADLAARLLLAPAELPIGIVTAFIGAPFFLFLLMR 342


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: 352
Number of extensions: 27
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: 345
Length adjustment: 28
Effective length of query: 304
Effective length of database: 317
Effective search space:    96368
Effective search space used:    96368
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.

Links

Downloads

Related tools

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