GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Burkholderia phytofirmans PsJN

Align UDP-glucose 4-epimerase (EC 5.1.3.2); UDP-N-acetylglucosamine 4-epimerase (EC 5.1.3.7) (characterized)
to candidate BPHYT_RS23350 BPHYT_RS23350 NAD-dependent epimerase/dehydratase

Query= BRENDA::Q9WYX9
         (309 letters)



>FitnessBrowser__BFirm:BPHYT_RS23350
          Length = 343

 Score =  185 bits (470), Expect = 1e-51
 Identities = 119/319 (37%), Positives = 184/319 (57%), Gaps = 20/319 (6%)

Query: 4   LVTGGAGFIGSHVVDKLIENGYGVIVVDNLSSGKVENLN--RNALFYEQ-----SIEDE- 55
           L+TG AGFIGS++++ L++    V+ +DN S+G   NL+  R+ +  EQ      IE + 
Sbjct: 20  LITGVAGFIGSNLLEALLKLDQTVVGLDNFSTGYQRNLDEVRSVVSPEQWKRFRFIEGDI 79

Query: 56  -EMMERIFSLHRPEYVFHLAAQASVAISVREPARDAKTNIIGSLVLLEKSIKYGVKKFIF 114
             + + + ++H  ++V H AA  SV  SV +P    + NI G L +L  +    V  F +
Sbjct: 80  RRLEDCVSAVHGVDHVLHEAALGSVPRSVADPIATHEVNISGFLNMLVAARDAQVSSFTY 139

Query: 115 SSTGGAIYGENVKVFPTPETEIPHPISPYGIAKYSTEMYLEFFAREYGLKYTVLRYANVY 174
           +++    YG+++ + P  E +I  P+SPY + KY+ E+Y   FAR YG K   LRY N +
Sbjct: 140 AASSST-YGDHLGL-PKVEDQIGQPLSPYAVTKYANELYASVFARAYGFKTIGLRYFNAF 197

Query: 175 GPRQDPYGE-AGVVAIFTERMLRGEEVHIFGDGEYVRDYVYVDDVVRANLLAM---EKGD 230
           G RQDP G  A V+  +T  ++ G++V I GDGE  RD+ +VD+VV+AN+LA    E   
Sbjct: 198 GKRQDPDGAYAAVIPKWTAALIAGDDVLINGDGETSRDFCFVDNVVQANILAAMSDETAR 257

Query: 231 NEVFNIGTGRGTTVNQLFKLLKEI-----TGYDKEPVYKPPRKGDVRKSILDYTKAKEKL 285
           NEV+N+  G  TT+ QL+  L+ +        DK PV+ P R GDVR S  +  KA+  L
Sbjct: 258 NEVYNVAVGDRTTLIQLYDGLRAVLTDNGVRCDKRPVFGPFRAGDVRHSQANVDKAERLL 317

Query: 286 GWEPKVSLEEGLKLTVEYF 304
           G+E ++S  EGL   + ++
Sbjct: 318 GYENRISFVEGLSRAMPWY 336


Lambda     K      H
   0.318    0.139    0.396 

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: 262
Number of extensions: 17
Number of successful extensions: 5
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: 309
Length of database: 343
Length adjustment: 28
Effective length of query: 281
Effective length of database: 315
Effective search space:    88515
Effective search space used:    88515
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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.

Links

Downloads

Related tools

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