GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Pseudomonas fluorescens FW300-N1B4

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate Pf1N1B4_3974 ABC transporter, ATP-binding protein

Query= reanno::Dino:3607124
         (338 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3974
          Length = 341

 Score =  244 bits (624), Expect = 2e-69
 Identities = 131/324 (40%), Positives = 197/324 (60%), Gaps = 3/324 (0%)

Query: 1   MAGIKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRI 60
           MA ++++ + K YG   A+   NL +E GEFV  +GPSGCGK+T L+ +AG   VSSGRI
Sbjct: 1   MAFVQLENLGKRYGEIDAVVATNLSVEKGEFVSLLGPSGCGKTTTLQMIAGFVEVSSGRI 60

Query: 61  EIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARV 120
            + GRD+T  +PA R L +VFQSYAL+PHMTVR+N+ FG+++     D  ++R+    ++
Sbjct: 61  VLDGRDITHAKPASRGLGVVFQSYALFPHMTVRDNVAFGLRMRKVPNDELQQRVDRVLKL 120

Query: 121 LQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLH 180
           ++L  + +R P +LSGGQRQRVA+ RA+V  P V L DEPLSNLDA LR +M+ E+  + 
Sbjct: 121 VRLNQHAERYPRELSGGQRQRVALARALVIEPPVLLLDEPLSNLDANLREEMQFEIRRIQ 180

Query: 181 KQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMN 240
           +++G T + VTHDQ EA++++D++VV+  GRI Q+ +P  LY  P + F++ F+G   + 
Sbjct: 181 REVGITTLMVTHDQSEALSISDRVVVMQAGRITQIDAPYTLYEHPRTEFISGFVGKANLL 240

Query: 241 VFSSDVG--LQDISLDASAAFVGCRPEHIEIVPDGDGHIAATVHVKERLGGESLLYLGLK 298
               D    +Q  + D     +  RPE I++   G G +   +  +  LG + L  +   
Sbjct: 241 PGERDSAGVVQVCNRDNGELTLSLRPEKIDLRDVGLGRLQGKIVSRFFLGSQWLYGVSTS 300

Query: 299 -GGGQIVARVGGDDETKVGAAVSL 321
            G   +V R  G      G AV L
Sbjct: 301 LGELSVVRRNDGSAPLIEGTAVGL 324


Lambda     K      H
   0.320    0.139    0.396 

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: 309
Number of extensions: 11
Number of successful extensions: 1
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: 338
Length of database: 341
Length adjustment: 28
Effective length of query: 310
Effective length of database: 313
Effective search space:    97030
Effective search space used:    97030
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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