GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Echinicola vietnamensis KMM 6221, DSM 17526

Align UDP-glucose 4-epimerase (EC 5.1.3.2); UDP-N-acetylglucosamine 4-epimerase (EC 5.1.3.7) (characterized)
to candidate Echvi_3799 Echvi_3799 Nucleoside-diphosphate-sugar epimerases

Query= BRENDA::Q9WYX9
         (309 letters)



>FitnessBrowser__Cola:Echvi_3799
          Length = 314

 Score =  140 bits (352), Expect = 5e-38
 Identities = 100/316 (31%), Positives = 169/316 (53%), Gaps = 17/316 (5%)

Query: 3   ILVTGGAGFIGSHVVDKLIENGYGVIVVDNLSSGKVENLNRNALFYEQSIEDEEMMERIF 62
           ILVTGG+GF+GSH+ D+L++ G  V+ VDNL +G+  N++   L  E++ E     +  F
Sbjct: 4   ILVTGGSGFLGSHLCDRLLKEGNEVLCVDNLFTGRKSNIHH--LLDEKNFEFLR-HDITF 60

Query: 63  SLH-RPEYVFHLAAQASVAISVREPARDAKTNIIGSLVLLEKSIKYGVKKFIFSSTGGAI 121
            L+   + +++LA  AS      +P + AKT++IG++ +L  + +  V+  I  ++   +
Sbjct: 61  PLYVEVDEIYNLACPASPVHYQFDPVQTAKTSVIGAINMLGLAKRLKVR--ILQASTSEV 118

Query: 122 YGENVKVFPTPETEIPHPISPYGI------AKYSTEMYLEFFAREYGLKYTVLRYANVYG 175
           YG+  ++ P PE+     ++  GI       K   E     + R++G+   V+R  N YG
Sbjct: 119 YGD-PELHPQPES-YKGSVNTTGIRACYDEGKRCAETLFFDYHRQHGVDIKVMRIFNTYG 176

Query: 176 PRQDPYGEAGVVAIFTERMLRGEEVHIFGDGEYVRDYVYVDDVVRA--NLLAMEKGDNEV 233
           PR  P  +  VV+ F  + L+GE++ IFGDG   R + YV+D++     L+    G    
Sbjct: 177 PRMHP-NDGRVVSNFIVQALKGEDITIFGDGLQTRSFCYVEDLIEGMYRLMNSRDGFTGP 235

Query: 234 FNIGTGRGTTVNQLFKLLKEITGYDKEPVYKPPRKGDVRKSILDYTKAKEKLGWEPKVSL 293
            NIG     T+ +L + + ++ G   +  + P  + D  +       AK++LGWEPKV L
Sbjct: 236 VNIGNPGEFTMLELAQEILDLVGSGSQLKFLPLPQDDPMQRQPIIHMAKKELGWEPKVRL 295

Query: 294 EEGLKLTVEYFRKTLE 309
            EGL  T+ YF + L+
Sbjct: 296 REGLIETINYFDRILK 311


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: 260
Number of extensions: 12
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: 314
Length adjustment: 27
Effective length of query: 282
Effective length of database: 287
Effective search space:    80934
Effective search space used:    80934
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 Apr 09 2024. 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