GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecD in Pseudomonas putida KT2440

Align iron(III) dicitrate transport system permease protein FecD (characterized)
to candidate PP_4688 PP_4688 Heme/hemin ABC transporter, permease protein

Query= CharProtDB::CH_004160
         (318 letters)



>FitnessBrowser__Putida:PP_4688
          Length = 345

 Score =  157 bits (398), Expect = 3e-43
 Identities = 118/343 (34%), Positives = 181/343 (52%), Gaps = 39/343 (11%)

Query: 7   IFITLALAGCAL---LSLHMGVIPVPWRALLTDWQAG-------------HEHYYVLMEY 50
           +FI+L+L  C L   LSL +G + +P   +    +AG              +   +L + 
Sbjct: 10  LFISLSLL-CLLAIWLSLALGPVSLP---MFDTLRAGLRLLGLPVSEDGLQQAEMILGQI 65

Query: 51  RLPRLLLALFVGAALAVAGVLIQGIVRNPLASPDILGVNHAASLASVGALL-------LM 103
           RLPR LL L VGA LA++GV +QG+ RNPLA P ++GV   A++ +  A++       + 
Sbjct: 66  RLPRTLLGLAVGAVLALSGVAMQGLFRNPLADPGLVGVAAGAAVGAAVAIVGGAWFGGMP 125

Query: 104 PSLPVMVLPLLAFAGGMAGLILLKMLAKTHQPMKLA---LTGVALSACW-ASLTDYLMLS 159
            +    +L   AF GG+    L+  L +      +A   L GVA++A   A++  +  L+
Sbjct: 126 DAFAPYLLSFCAFVGGLGVTALVYRLGRRDGQTNVATMLLAGVAMTALGGAAVGLFSYLA 185

Query: 160 RPQDVNNALLWLTGSLWG----RDWSFVKIAIPLMILFLPLSLSFCRDLDLLALGDARAT 215
               +     W  GSL G    R W  + +A  + + +LP      + L+ L LG++ A 
Sbjct: 186 DDATLRTLTFWNLGSLNGASYERLWPLLLVATGVAV-WLPRR---AKALNALLLGESEAR 241

Query: 216 TLGVSVPHTRFWALLLAVAMTSTGVAACGPISFIGLVVPHMMRSITGGRHRRLLPVSALT 275
            LGV V   +   +          VAA G I FIGLVVPH++R + G  HR +LP S L 
Sbjct: 242 HLGVDVERLKRELVFCTALGVGAAVAAAGLIGFIGLVVPHLVRLLAGPDHRVVLPASLLA 301

Query: 276 GALLLVVADLLARIIHPPLELPVGVLTAIIGAPWFVWLLVRMR 318
           G +L++ ADL AR++  P ELP+G++TA IGAP+F++LL+R R
Sbjct: 302 GGVLMLFADLAARLLLAPAELPIGIVTAFIGAPFFLFLLMRGR 344


Lambda     K      H
   0.330    0.142    0.447 

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: 300
Number of extensions: 15
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: 318
Length of database: 345
Length adjustment: 28
Effective length of query: 290
Effective length of database: 317
Effective search space:    91930
Effective search space used:    91930
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 (21.8 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