GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecD in Pseudomonas fluorescens FW300-N2E2

Align iron(III) dicitrate transport system permease protein FecD (characterized)
to candidate Pf6N2E2_3546 ABC transporter (iron.B12.siderophore.hemin) , permease component

Query= CharProtDB::CH_004160
         (318 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_3546
          Length = 336

 Score =  186 bits (473), Expect = 5e-52
 Identities = 118/330 (35%), Positives = 175/330 (53%), Gaps = 19/330 (5%)

Query: 4   ALVIFITLALAGCALLSLHMGVIPVP----WRALLTD--------WQAGHEHYYVLMEYR 51
           AL++F+   L    ++SL  G   VP    W  LL          W  G EH   L+  R
Sbjct: 8   ALLMFLGALLLVSCVVSLGFGPARVPVAVVWDILLNKAFGVGSAYWSPGQEHIVWLI--R 65

Query: 52  LPRLLLALFVGAALAVAGVLIQGIVRNPLASPDILGVNHAASLASVGALLLMPSLP-VMV 110
           +PRLLL   VGA LA+ G ++Q + RNPLA P +LGV   A+L +V  +L +  +  ++ 
Sbjct: 66  VPRLLLGALVGAGLALIGAVLQAVTRNPLADPHLLGVTSGATLGAVIVVLHVGEIVGLLT 125

Query: 111 LPLLAFAGGMAGLILLKMLAKTHQPM---KLALTGVALSACWASLTDYLMLSRPQDVNNA 167
           LPL AF G +  ++L+  +A     +   +L L GVA+S    +  + L+       ++A
Sbjct: 126 LPLAAFIGALLSMLLVLTIAARQGRLESDRLLLCGVAVSFVMMAAANLLLFLGDHRASSA 185

Query: 168 LL-WLTGSLWGRDWSFVKIAIPLMILFLPLSLSFCRDLDLLALGDARATTLGVSVPHTRF 226
           ++ W+ G L    W  + +    ++L L L L   R L+ L  G+  A TLG++    R 
Sbjct: 186 VMFWMLGGLGLARWELLAVPAASVVLGLVLLLGMARPLNALMAGEQTAVTLGLNAAKVRL 245

Query: 227 WALLLAVAMTSTGVAACGPISFIGLVVPHMMRSITGGRHRRLLPVSALTGALLLVVADLL 286
           W  L+A  MT   V+  G I F+GL+VPH+ R + G  HRRLLP   L G+L LV  D+ 
Sbjct: 246 WIFLIASLMTGVLVSISGSIGFVGLMVPHIARRLVGAEHRRLLPACVLLGSLFLVWVDVA 305

Query: 287 ARIIHPPLELPVGVLTAIIGAPWFVWLLVR 316
           AR +  P +LP+GV TA IG  +F+ L+ R
Sbjct: 306 ARTLIAPEDLPIGVATAAIGGLFFIGLMRR 335


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: 307
Number of extensions: 9
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: 318
Length of database: 336
Length adjustment: 28
Effective length of query: 290
Effective length of database: 308
Effective search space:    89320
Effective search space used:    89320
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: 48 (23.1 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