GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Paraburkholderia bryophila 376MFSha3.1

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate H281DRAFT_02703 H281DRAFT_02703 monosaccharide ABC transporter membrane protein, CUT2 family

Query= uniprot:A0A1N7UKA9
         (325 letters)



>FitnessBrowser__Burk376:H281DRAFT_02703
          Length = 333

 Score =  251 bits (641), Expect = 2e-71
 Identities = 132/299 (44%), Positives = 201/299 (67%), Gaps = 5/299 (1%)

Query: 32  ILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVILTKGIDLSVGSILAFAGLC 91
           +++C+ ++ +S  F+T     +I+ Q S+ GI AVG T+VI+T GIDLSVGS++A  G+ 
Sbjct: 34  VIICIALSIASPEFLTTSTLTNIMVQVSVVGIAAVGGTFVIITSGIDLSVGSLVALTGMV 93

Query: 92  SAMV----ATQGYGL-LAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSIARGMT 146
           +A V    +    GL +A + A +  GA  G +NG  VA L + PF+ TL M+++ARG+T
Sbjct: 94  AATVMAGSSPGAIGLGIAGLCAALAVGAAAGALNGLAVAWLRLVPFIVTLAMMAMARGLT 153

Query: 147 FILNDGSPITDLPDAYLALGIGKIGPIGVPIIIFAVVALIFWMVLRYTTYGRYVYAVGGN 206
             ++DG    D P+A+ A G   +  + +P+I+  V+ +I  ++LR TT+G  V+AVGGN
Sbjct: 154 LAISDGRTKFDFPNAFTAFGAKTVAGLPMPMIVMLVIFVIGHVLLRKTTFGHQVFAVGGN 213

Query: 207 EKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYELDAIAAVVIGG 266
           +++AR +GI V +V+F  Y+++G+ A +AG+VL+ R  SALP A    EL  IAAVVIGG
Sbjct: 214 QEAARLAGIPVHRVVFLTYMLAGVTAAIAGIVLAGRLNSALPSAANGLELQVIAAVVIGG 273

Query: 267 TSLSGGTGSIVGTLFGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAVLIDVWRKKKR 325
           TSL+GG GSIVGT  G +LIGVIN GL+LLGV+ ++ Q  +G +I  AVL+D   ++++
Sbjct: 274 TSLAGGRGSIVGTFIGVVLIGVINVGLSLLGVNPFWTQFIQGGVIFAAVLLDALSQRRK 332


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: 286
Number of extensions: 16
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: 325
Length of database: 333
Length adjustment: 28
Effective length of query: 297
Effective length of database: 305
Effective search space:    90585
Effective search space used:    90585
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