GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Phyllobacterium brassicacearum STM 196

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate WP_106714415.1 CU102_RS28780 ABC transporter permease

Query= uniprot:A0A1N7UKA9
         (325 letters)



>NCBI__GCF_003010955.1:WP_106714415.1
          Length = 342

 Score =  259 bits (662), Expect = 7e-74
 Identities = 147/346 (42%), Positives = 215/346 (62%), Gaps = 27/346 (7%)

Query: 1   MNAKTITAPVTA---APRNRLRLS------LDRFGLPLVFILLCVVMAFSSEYFMTWRNW 51
           M ++ +TA  T     PR+R RL       L   G+ L+F +L  + A  S + M ++  
Sbjct: 1   MTSEPVTAKATTPTLTPRSRRRLPPEVNILLVLIGIALIFEILGWIFAGQS-FLMNFQRL 59

Query: 52  MDILRQTSINGILAVGMTYVILTKGIDLSVGSILAFAGLCSAMVATQG------YGLLA- 104
             I+ Q S+ GI+AVG+T VI+T GIDLS GS++    + +A  A         Y  L  
Sbjct: 60  RIIILQVSVIGIIAVGVTQVIITGGIDLSSGSVVGMTAMIAASFAQSSTWARPVYPALTD 119

Query: 105 -----AVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSIARGMTFILNDGSPITDLP 159
                 +  G+  G + G+VNG+++A   IPPF+ATLGM+  ARG+      GSP++ L 
Sbjct: 120 LPFFIPIGVGLGIGLLAGIVNGWLIAYTKIPPFIATLGMMVSARGVAKWYTKGSPVSGLT 179

Query: 160 DAYLALGIGKIGPIGVPIIIFAVVALIFWMVLRYTTYGRYVYAVGGNEKSARTSGIGVRK 219
           D +  +G         P+++F +VALIF + LRYT YG++ YA+G N ++AR SGI + +
Sbjct: 180 DQFTFIGASIW-----PVVVFLLVALIFHVALRYTRYGKFTYAIGANLQAARVSGIDIER 234

Query: 220 VMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYELDAIAAVVIGGTSLSGGTGSIVGT 279
            +  VY ++GLLAGLAG+V +AR  +A    GV+YELDAIAA VIGGTSL+GG G I GT
Sbjct: 235 HLIKVYAIAGLLAGLAGIVTAARAQTAQAGMGVTYELDAIAAAVIGGTSLTGGIGRITGT 294

Query: 280 LFGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAVLIDVWRKKKR 325
           + GA+++GV+ +G   L V +YYQ++ KG+IIV AV++DV+R+KKR
Sbjct: 295 VIGAIILGVMISGFTFLRVDAYYQEIIKGVIIVAAVIVDVYRQKKR 340


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: 314
Number of extensions: 17
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: 342
Length adjustment: 28
Effective length of query: 297
Effective length of database: 314
Effective search space:    93258
Effective search space used:    93258
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 24 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