GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruII-ABC in Tatumella morbirosei LMG 23360

Align The fructose-specific PTS Enzyme IIABC FruA (characterized)
to candidate WP_038021225.1 HA49_RS06185 PTS fructose transporter subunit EIIC

Query= TCDB::Q0S1N2
         (700 letters)



>NCBI__GCF_000757425.2:WP_038021225.1
          Length = 360

 Score =  244 bits (622), Expect = 7e-69
 Identities = 140/341 (41%), Positives = 202/341 (59%), Gaps = 22/341 (6%)

Query: 336 RQVLLTGVSYMIPFVAAGGLLIALGFLLGGYEISGPAEDIVLSNSLGQLPEGGLATYLGA 395
           RQ L+TGVSYMIPFV +GG+L+A+  +  G                G +P+   A  L  
Sbjct: 12  RQHLMTGVSYMIPFVVSGGILLAVAVMFYGK---------------GAVPDAESAANLKK 56

Query: 396 VLFQLGSLAFSFLVPALAGYIAFAIADRPGLAPGFTAGAVAVFVGAGFIGGLVGGLIAGV 455
            LF +G    + +VP LA YI ++I++R  LAP   A  V    GAGF G L+ G+I G+
Sbjct: 57  -LFDIGVAGLTLMVPFLAAYIGYSISERSALAPCAIAAWVGNSFGAGFFGALIAGIIGGI 115

Query: 456 VALWISRIPVPQWLRGLMPVVIIPLFATLIVGALMFLVLGRPLASITSGLTNWLNGLSGS 515
           V  ++ +IPV + LR +MP+ +IP+  TLI   +M   LG P+  +T  LT WL G+   
Sbjct: 116 VVYYLKKIPVHKVLRSVMPIFVIPVIGTLITAGIMMWGLGEPVGMLTKSLTVWLQGMQQG 175

Query: 516 SVIFLGIILGLMMCFDLGGPVNKAAYAFAVAGLNVNDPASLRIMAAVMAAGMVPPLAMAL 575
           SV+ L +I+GLM+ FD+GGPVNK AYAF +  +         ++A    +  +PPL + L
Sbjct: 176 SVVILAVIMGLMLAFDMGGPVNKVAYAFMLICV---AQGVYHVVAIAAVSICIPPLGLGL 232

Query: 576 ASTVLRPSLFSEAERENGKAAWLLGSAFISEGAIPFAAADPLRVIPSMMAGGAVTGALIM 635
           A+ + R + FS  E+E GKAA ++G   ++EGAIPFAA+DPLRVIPS+M  G+V+GA++ 
Sbjct: 233 ATLIGRRN-FSAEEQEAGKAALVMGCVGVTEGAIPFAASDPLRVIPSIML-GSVSGAVVA 290

Query: 636 AF-DVTLSAPHGGIFVFFAIGNLLWFLVALAAGVVVAALCV 675
           A       A  GG+ V   +     +L+A+  G+VV ALCV
Sbjct: 291 ALTGAECYAGWGGLIVLPVVSGKFGYLLAVVTGMVVTALCV 331


Lambda     K      H
   0.320    0.136    0.395 

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: 609
Number of extensions: 29
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: 700
Length of database: 360
Length adjustment: 34
Effective length of query: 666
Effective length of database: 326
Effective search space:   217116
Effective search space used:   217116
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 52 (24.6 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