GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruF in Phaeobacter inhibens BS107

Align Fructose import permease protein FruF (characterized)
to candidate GFF716 PGA1_c07310 binding protein dependent transport system permease

Query= SwissProt::Q8G846
         (356 letters)



>FitnessBrowser__Phaeo:GFF716
          Length = 373

 Score =  128 bits (321), Expect = 3e-34
 Identities = 96/303 (31%), Positives = 155/303 (51%), Gaps = 39/303 (12%)

Query: 63  QESARYLMIATGMTLVISTAGIDLSVGSVMAVAGAA-AMQTLSNGMNVWLSILIALAVGL 121
           Q SA++++IA G  L++     DLSVGS++  AG   A+ +++ G  VWL+IL+  A+  
Sbjct: 62  QISAQFMIIAVGACLLMIAGEFDLSVGSMIGFAGMLIAIFSVTLGWPVWLAILVTFAIAT 121

Query: 122 AIGCVNGALVSFLGLQPFITTLIMMLAGRGMA---------KVITSG-----ENTDASAV 167
           AIG +NG +V   GL  FI TL  +   RG A         K I  G     E    +A+
Sbjct: 122 AIGALNGFIVVRTGLPSFIVTLAFLFILRGFAIYLPQTIERKTIIGGVADAAEGDWLAAL 181

Query: 168 AGNEPL----KWFA-NGFIL--------------GIPANFVIAVIIVILVGLLCRKTAMG 208
            G + L    +WF  NG+I               G+P   V A+++VI+  ++  KT  G
Sbjct: 182 FGGKILTGLFQWFGDNGWIAVFERGTRKGQPVVEGLPMLIVWAILLVIIGHVILTKTRFG 241

Query: 209 MMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAAIAGLFATASVMRVDVVKTGQDL-- 266
             I A G + EA+R +G+   ++  L++  + F A +   FAT  VM      + + L  
Sbjct: 242 NWIFAAGGDAEAARNSGVPVNRVKILMFMFTAFCATV---FATCQVMEFGGAGSDRGLLK 298

Query: 267 EMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKTIITLGVNAEATPAFFAVVVIVI 326
           E  AI+AVVIGG  L GG  S+ G+A+GA+I  ++++ +   GV +     F  ++++  
Sbjct: 299 EFEAIIAVVIGGALLTGGYGSVLGAALGALIFGVVQQGLFFAGVESSLFRVFLGLILLFA 358

Query: 327 CVM 329
            ++
Sbjct: 359 VIL 361


Lambda     K      H
   0.325    0.136    0.384 

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: 320
Number of extensions: 26
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: 356
Length of database: 373
Length adjustment: 29
Effective length of query: 327
Effective length of database: 344
Effective search space:   112488
Effective search space used:   112488
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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