GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Pseudomonas fluorescens FW300-N1B4

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate Pf1N1B4_4287 Inositol transport system permease protein

Query= uniprot:A0A1N7UKA9
         (325 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4287
          Length = 340

 Score =  262 bits (670), Expect = 8e-75
 Identities = 150/336 (44%), Positives = 211/336 (62%), Gaps = 20/336 (5%)

Query: 4   KTITAPVTAAPR--NRLRLSLDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTSIN 61
           K    PV +  R    L + L   G+ LVF +   ++   S + M  +  + ++ Q SI 
Sbjct: 8   KPAAVPVKSRRRFPTELSIFLVLIGIGLVFEMFGWIVRDQS-FLMNSQRLVLMILQVSII 66

Query: 62  GILAVGMTYVILTKGIDLSVGSILAFAGLCSAMVATQGYGLLAA------------VSAG 109
           G+LA+G+T VI+T GIDLS GS+LA + + +A +A       A             V  G
Sbjct: 67  GLLAIGVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFARAVFPSLTDLPVWIPVIVG 126

Query: 110 MFAGAMLGVVNGFMVANLSIPPFVATLGMLSIARGMTFILNDGSPITDLPDAYLALGIGK 169
           +  G + G +NG ++A   IPPF+ATLGM+  ARG+     +G P++ L D+Y A+G G 
Sbjct: 127 LGVGLLAGAINGSIIAITGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGHG- 185

Query: 170 IGPIGVPIIIFAVVALIFWMVLRYTTYGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSG 229
                +P+IIF VVA+IF + LRYT YG+Y YA+GGN ++ARTSGI V++ +  VY ++G
Sbjct: 186 ----AMPVIIFLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLVIVYSIAG 241

Query: 230 LLAGLAGVVLSARTTSALPQAGVSYELDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVI 289
           LLAGLAGVV SAR  +     G+SYELDAIAA VIGGTSL+GG G I GT+ GAL++GV+
Sbjct: 242 LLAGLAGVVASARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVM 301

Query: 290 NNGLNLLGVSSYYQQVAKGLIIVFAVLIDVWRKKKR 325
            +G   +GV +Y Q + KGLIIV AV+ID +R K++
Sbjct: 302 ASGFTFVGVDAYIQDIIKGLIIVVAVVIDQYRNKRK 337


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: 291
Number of extensions: 14
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: 340
Length adjustment: 28
Effective length of query: 297
Effective length of database: 312
Effective search space:    92664
Effective search space used:    92664
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