GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Acidovorax sp. GW101-3H11

Align Fructose import permease protein FruG (characterized)
to candidate Ac3H11_2880 Ribose ABC transport system, permease protein RbsC (TC 3.A.1.2.1)

Query= SwissProt::Q8G845
         (340 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2880
          Length = 350

 Score =  150 bits (379), Expect = 5e-41
 Identities = 94/314 (29%), Positives = 167/314 (53%), Gaps = 16/314 (5%)

Query: 26  LAAVVIFILMIIMGQALFGTYIRLGFISSLFIDHAYLIILAVAMTLPILTGGIDLSVGAI 85
           L  V+  +L+ I G  L   +     + ++    A++ I+AV M   I++GGIDLSVG++
Sbjct: 41  LGPVIGLVLLCIAGTLLNSNFATYDNVMNVLTRTAFIGIIAVGMCFVIISGGIDLSVGSM 100

Query: 86  VAITAVVGLKLANA-----GVPAFLVMIIMLL---IGAVFGLLAGTLIEEFNMQPFIATL 137
            A+ A   +   NA     G P   V++ MLL   +GAVFGL+ G LI +  ++PFI TL
Sbjct: 101 AALIAGSVILFMNAMAPVLGSPMAAVVVGMLLAVVLGAVFGLVHGLLITKGRIEPFIVTL 160

Query: 138 STMFLARGLASIISTDSLTFPQGNDFSFISNVIKIIDNPKISNDLSFNVGVIIALVVVVF 197
            T+ + R   +        F  G   +  +++  I      +N L   + V I L+V + 
Sbjct: 161 GTLGIFRAYLTY-------FSNGGAITLENDLSDIYSPVYYANLLGVPIPVWIFLLVAIV 213

Query: 198 GYVFLHHTRTGRTIYAIGGSRSSAELMGLPVKRTQYIIYLTSATLAALASIVYTANIGSA 257
           G V L+ T  GR + AIG +   A+   + V + + + Y+       +A+++Y   +GSA
Sbjct: 214 GGVILNRTAYGRYVQAIGSNEQVAQYAAVDVHKIKILTYMLLGVCVGIATLLYVPRLGSA 273

Query: 258 KNTVGVGWELDAVASVVIGGTIITGGFGYVLGSVLGSLVRSILDPLTSDFGVPAEWTTIV 317
             T G+ WEL+A+A+V++GGT++ GG G + G+V+G+++ S++  + +   + + +    
Sbjct: 274 SPTTGLLWELEAIAAVIVGGTVLKGGAGSITGTVVGAILLSVISNILNLTSIISVYLNAA 333

Query: 318 I-GLMILVFVVLQR 330
           + G +I+    +QR
Sbjct: 334 VQGFVIIAVAFMQR 347


Lambda     K      H
   0.327    0.142    0.400 

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: 301
Number of extensions: 22
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: 340
Length of database: 350
Length adjustment: 29
Effective length of query: 311
Effective length of database: 321
Effective search space:    99831
Effective search space used:    99831
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 (21.7 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