GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Klebsiella michiganensis M5al

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate BWI76_RS07245 BWI76_RS07245 ABC transporter

Query= uniprot:A0A1N7UKA9
         (325 letters)



>FitnessBrowser__Koxy:BWI76_RS07245
          Length = 343

 Score =  260 bits (664), Expect = 4e-74
 Identities = 148/345 (42%), Positives = 208/345 (60%), Gaps = 26/345 (7%)

Query: 2   NAKTITAPVTAAP------RNRLRLSLDRFGLPLVFILLCVVMAF---SSEYFMTWRNWM 52
           N K    PVT  P      R+RL      F + LV  L   +  +      + +     +
Sbjct: 3   NMKITATPVTEKPSFFGQLRHRLPKDTGIFIVMLVIALTFEIAGWYVRDQSFLLNTNRLI 62

Query: 53  DILRQTSINGILAVGMTYVILTKGIDLSVGSILAFAGLCSAMVATQGYGL---------- 102
            I+ Q +I GI+AVG+T VI+T GIDLS GS++A A + +A +A     L          
Sbjct: 63  LIVLQVAIIGIIAVGVTQVIITTGIDLSSGSVIALAAVVAASLAQTSDSLSPMFPSLVNM 122

Query: 103 --LAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSIARGMTFILNDGSPITDLPD 160
             +  + AG+  G + G+ NGF+V    IPPF+ATLGM+  ARG+      G+PI+ L D
Sbjct: 123 PAIIPIGAGIGVGLLCGLTNGFLVTRTGIPPFIATLGMMVSARGLAQYYTQGNPISFLSD 182

Query: 161 AYLALGIGKIGPIGVPIIIFAVVALIFWMVLRYTTYGRYVYAVGGNEKSARTSGIGVRKV 220
           ++ A+G G      +P+IIF VVA +F + L++T YG+YVYA+GGN  SA+ SGI V K 
Sbjct: 183 SFTAIGQG-----AMPVIIFFVVAAVFHIALKHTRYGKYVYAIGGNMTSAKVSGINVNKY 237

Query: 221 MFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYELDAIAAVVIGGTSLSGGTGSIVGTL 280
           +  VY ++G L+GLAGVVL+AR +S     G+SYELDAIAA VIGG+SL GG G I GTL
Sbjct: 238 LVIVYAIAGALSGLAGVVLAARVSSGQSSMGMSYELDAIAAAVIGGSSLMGGVGRITGTL 297

Query: 281 FGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAVLIDVWRKKKR 325
            GA+++G+I +G   +GV +Y Q + KG+IIV AV ID+ R +K+
Sbjct: 298 IGAMILGLIKSGFTFVGVDAYVQDIIKGIIIVAAVTIDMRRNRKK 342


Lambda     K      H
   0.326    0.141    0.412 

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: 263
Number of extensions: 11
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: 325
Length of database: 343
Length adjustment: 28
Effective length of query: 297
Effective length of database: 315
Effective search space:    93555
Effective search space used:    93555
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 (21.6 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