GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruII-ABC in Photobacterium gaetbulicola Gung47

Align The fructose-specific PTS Enzyme IIABC FruA (characterized)
to candidate WP_044620523.1 H744_RS00360 PTS fructose transporter subunit EIIC

Query= TCDB::Q0S1N2
         (700 letters)



>NCBI__GCF_000940995.1:WP_044620523.1
          Length = 353

 Score =  256 bits (653), Expect = 2e-72
 Identities = 152/362 (41%), Positives = 213/362 (58%), Gaps = 25/362 (6%)

Query: 335 LRQVLLTGVSYMIPFVAAGGLLIALGFLLGGYEISGPAEDIVLSNSLGQLPEGGLATYLG 394
           L++ LLTG S+M+PFV AGG+L+AL  +LGG                G +PEG    +L 
Sbjct: 8   LKRHLLTGTSHMLPFVVAGGVLLALSVMLGGK---------------GAVPEG---VFLE 49

Query: 395 AVLFQLGSLAFSFLVPALAGYIAFAIADRPGLAPGFTAGAVAVFVGAGFIGGLVGGLIAG 454
             L+ +G   F+  VP L GYIA++IADRP LAPG     +A  V AGF+G +V G IAG
Sbjct: 50  G-LWDMGIAGFTLFVPVLGGYIAYSIADRPALAPGMIGAYLANQVQAGFLGAIVVGFIAG 108

Query: 455 VVALWISRIPVPQWLRGLMPVVIIPLFATLIVGALMFLVLGRPLASITSGLTNWLNGLSG 514
            V L + RIP+   L+ +    I+P+  T IV  L+  V+G P+A     +  WL G++G
Sbjct: 109 YVVLQLKRIPLSNKLKAISTYFILPIGGTFIVSGLVIWVIGTPIAMAMESMNLWLQGMAG 168

Query: 515 SSVIFLGIILGLMMCFDLGGPVNKAAYAFAVAGLNVNDPASLRIMAAVMAAGMVPPLAMA 574
           +S  FLG++LG M  FD+GGP+NK A  FA   +         +M  V  A  VPPL M 
Sbjct: 169 ASKAFLGMVLGGMTAFDMGGPINKVATLFAQTQVGTQP----WLMGGVGIAICVPPLGMF 224

Query: 575 LASTVLRPSLFSEAERENGKAAWLLGSAFISEGAIPFAAADPLRVIPSMMAGGAVTGALI 634
           LA T+L P  +++ ERE GKAA ++G   I+EGAIPFAAADP+RV+PS++ GG V   + 
Sbjct: 225 LA-TLLSPKRYTDEEREAGKAAGIMGCIGITEGAIPFAAADPMRVLPSIVVGGMVGNVVG 283

Query: 635 MAFDVTLSAPHGGIFVFFAIGNLLWFLVALAAGVVVAALCVVGAKEFIKPGASDAELDPD 694
             F+V   AP GG+ V   +   L+++V +AAG +  AL V   K+ I+    DA+++ D
Sbjct: 284 FMFNVLNHAPWGGLIVLPVVDGRLFYIVGIAAGALTTALMVNALKKPIEQ-RQDAKVEND 342

Query: 695 VA 696
            A
Sbjct: 343 SA 344


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: 618
Number of extensions: 33
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: 353
Length adjustment: 34
Effective length of query: 666
Effective length of database: 319
Effective search space:   212454
Effective search space used:   212454
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