GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Escherichia coli BW25113

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate 17810 b3750 ribose ABC transporter permease protein (NCBI)

Query= uniprot:A0A1N7UKA9
         (325 letters)



>FitnessBrowser__Keio:17810
          Length = 321

 Score =  276 bits (707), Expect = 4e-79
 Identities = 150/303 (49%), Positives = 203/303 (66%), Gaps = 9/303 (2%)

Query: 22  LDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVILTKGIDLSV 81
           +++  L  + +L+ +V   S  +F T  N  +IL+QTS+N I+AVGMT VILT GIDLSV
Sbjct: 18  MEQKSLIALLVLIAIVSTLSPNFF-TINNLFNILQQTSVNAIMAVGMTLVILTSGIDLSV 76

Query: 82  GSILAFAGLCSAMVATQGYGLLAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSI 141
           GS+LA  G  +A +       L AV+A +  GA +G V G +VA   +  F+ATL M+ +
Sbjct: 77  GSLLALTGAVAASIVGIEVNALVAVAAALALGAAIGAVTGVIVAKGRVQAFIATLVMMLL 136

Query: 142 ARGMTFILNDGSPI----TDLPDAYLALGIGKIGPIGVP--IIIFAVVALIFWMVLRYTT 195
            RG+T +  +GSP+    T+  D +   GIG+  P+GVP  + I  +V L  W +L +T 
Sbjct: 137 LRGVTMVYTNGSPVNTGFTENADLFGWFGIGR--PLGVPTPVWIMGIVFLAAWYMLHHTR 194

Query: 196 YGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYE 255
            GRY+YA+GGNE + R SGI V K+   VY + GLLA LAG++  AR +SA P AG  YE
Sbjct: 195 LGRYIYALGGNEAATRLSGINVNKIKIIVYSLCGLLASLAGIIEVARLSSAQPTAGTGYE 254

Query: 256 LDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAV 315
           LDAIAAVV+GGTSL+GG G IVGTL GAL++G +NNGLNLLGVSSYYQ + K ++I+ AV
Sbjct: 255 LDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQMIVKAVVILLAV 314

Query: 316 LID 318
           L+D
Sbjct: 315 LVD 317


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: 231
Number of extensions: 6
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: 321
Length adjustment: 28
Effective length of query: 297
Effective length of database: 293
Effective search space:    87021
Effective search space used:    87021
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: 48 (23.1 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