GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araWsh in Dyella japonica UNC79MFTsu3.2

Align Inner-membrane translocator (characterized, see rationale)
to candidate N515DRAFT_2415 N515DRAFT_2415 simple sugar transport system permease protein

Query= uniprot:A0KWY6
         (405 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2415
          Length = 337

 Score =  124 bits (311), Expect = 4e-33
 Identities = 103/339 (30%), Positives = 166/339 (48%), Gaps = 20/339 (5%)

Query: 48  NARYQAGKSTSMGRYLW-------PLLALSILLLANLFIDSSFFNISYQDDRLYGSLIDI 100
           NA   A  S + GR  W       PLL   +L +A        ++           LID 
Sbjct: 2   NAVAPAATSAAAGRRPWWRRRAQVPLLVTLVLFVAMAGAGGVLYHGFLTPQVFLNLLID- 60

Query: 101 LNRSAPVALLSIGMSLVIATGGIDLSVGAVMAIAGAVCANLLLVPDISLVTVIAAGLIVG 160
              +A + ++++GM+ VI  GGIDLSVGAV+A +  + A L+       +  IA  L VG
Sbjct: 61  ---NAFLCIVAVGMTFVILAGGIDLSVGAVVAFSTVLLAELVQRHGWPPLAAIALVLAVG 117

Query: 161 LLAGCINGGLVSFLGIQPIVATLLLMVAGRGVAQLINQGQIITFQHPGFAAIG-----VG 215
              G   G L+    +QP V TL  M   RGVA LI+    I    P  A++      +G
Sbjct: 118 TGFGAGMGVLIQRFRLQPFVVTLAGMFLARGVATLISVDS-IDIDQPWLASVANLRLPLG 176

Query: 216 QFLGLPMPVWIVIGMLTFSQLLLRKTALGLFIEAVGCNAKASRYLGINDKSIKLFAYGIA 275
               L +   + + ++    LL   ++ G  + A+G +  ++R +G+   +  +  Y ++
Sbjct: 177 GGSMLSVGALVALAVVAAGALLAGASSFGRTVYAIGGSESSARLMGLPVDATVVRVYALS 236

Query: 276 GLCAALAGMISTADIQGSDANNAGLWLELDAVLAVVIGGAALTGGRFSLILSVVGALIIQ 335
           G CAALAG++ T  +    + +A L LELDA+ AVVIGG  L GG   ++ +++G L++ 
Sbjct: 237 GFCAALAGVVYTLYMLSGYSQHA-LGLELDAIAAVVIGGTVLAGGSGYVLGTLLGVLVLG 295

Query: 336 TLATTIIVSG-LPAKFNLLIKAIVILTVLLLQSAKFRRQ 373
            + T I+  G L + +  ++   ++L   LLQ   FRR+
Sbjct: 296 LIQTLIVFDGELSSWWTRIVIGALLLAFCLLQRL-FRRK 333


Lambda     K      H
   0.323    0.136    0.379 

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: 333
Number of extensions: 20
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: 405
Length of database: 337
Length adjustment: 30
Effective length of query: 375
Effective length of database: 307
Effective search space:   115125
Effective search space used:   115125
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 (22.0 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