GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c07310 in Caulobacter crescentus NA1000

Align Inositol transport system permease protein (characterized)
to candidate CCNA_00904 CCNA_00904 inositol ABC transport system, permease protein IatP

Query= reanno::Phaeo:GFF716
         (373 letters)



>FitnessBrowser__Caulo:CCNA_00904
          Length = 332

 Score =  126 bits (316), Expect = 1e-33
 Identities = 101/325 (31%), Positives = 150/325 (46%), Gaps = 41/325 (12%)

Query: 46  AGDSGMFNSQGVMNWSQISAQFMIIAVGACLLMIAGEFDLSVGSMIGFAGMLIAIFSVTL 105
           A +     ++  +N     + + IIAVG   +++ G  D++VGS++ FA +  A     +
Sbjct: 41  AANERFLTARNALNILSEVSIYGIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAV 100

Query: 106 ---GWPVWL-AILVTFAIATAIGALNGFIVVRTGLPSFIVTLAFLFILRGFAIYLPQTIE 161
              G   WL A+LV+  I  A G + G  V    +P+FIVTL  + + RG  + L     
Sbjct: 101 VGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGP 160

Query: 162 RKTIIGGVADAAEGDWLAALFGGKILTGLFQWFGDNGWIAVFERGTRKGQPVVEGLPMLI 221
               I G  DA                  ++W+G    +                LP+ +
Sbjct: 161 ----ISGFNDA------------------YRWWGSGEILF---------------LPVPV 183

Query: 222 VWAILLVIIGHVILTKTRFGNWIFAAGGDAEAARNSGVPVNRVKILMFMFTAFCATVFAT 281
           V   L+   GHV L  TR+G  ++A GG+AEAAR SGV V+ +   ++      A +   
Sbjct: 184 VIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGF 243

Query: 282 CQVMEFGGAGSDRGLLKEFEAIIAVVIGGALLTGGYGSVLGAALGALIFGVVQQGLFFAG 341
                 G A +  G   E   I +VVIGGA LTGG G V G  LGAL+ GV+  GL    
Sbjct: 244 LLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLH 303

Query: 342 VESSLFRVFLGLILLFAVILNTYIR 366
           V S + +V +GLI++ AV  + Y R
Sbjct: 304 VTSYVQQVVIGLIIVAAVAFDHYAR 328


Lambda     K      H
   0.330    0.145    0.443 

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: 450
Number of extensions: 29
Number of successful extensions: 3
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: 373
Length of database: 332
Length adjustment: 29
Effective length of query: 344
Effective length of database: 303
Effective search space:   104232
Effective search space used:   104232
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