GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Thiothrix lacustris DSM 21227

Align UDP-glucose 4-epimerase (EC 5.1.3.2); UDP-N-acetylglucosamine 4-epimerase (EC 5.1.3.7) (characterized)
to candidate WP_084260329.1 Q394_RS0103155 Vi polysaccharide biosynthesis UDP-N-acetylglucosaminuronic acid C-4 epimerase TviC

Query= BRENDA::Q9WYX9
         (309 letters)



>NCBI__GCF_000621325.1:WP_084260329.1
          Length = 344

 Score =  177 bits (450), Expect = 2e-49
 Identities = 118/325 (36%), Positives = 179/325 (55%), Gaps = 30/325 (9%)

Query: 4   LVTGGAGFIGSHVVDKLIENGYGVIVVDNLSSGKVENLNR-----------NALFYEQSI 52
           LVTG AGFIGS++++ L++    V+ +DN ++G   NL+            N  F    I
Sbjct: 21  LVTGVAGFIGSNLLETLLKLNQRVVGLDNFATGHQHNLDEVQSLVNREQWANFRFIRGDI 80

Query: 53  EDEEMMERIFSLHRPEYVFHLAAQASVAISVREPARDAKTNIIGSLVLLEKSIKYGVKKF 112
              ++ +   +    +YV H AA  SV  S+ +P     TNI G L +L  +    VK+F
Sbjct: 81  R--QLSDCQAACEGVDYVLHQAALGSVPRSLEDPITTNGTNIDGFLNMLVAARDAQVKRF 138

Query: 113 IFSSTGGAIYGENVKVFPTPETEIPHPISPYGIAKYSTEMYLEFFAREYGLKYTVLRYAN 172
           +++++    YG++    P  E  I  P+SPY + KY  E+Y + FAR YG     LRY N
Sbjct: 139 VYAASSST-YGDH-PALPKIEENIGKPLSPYAVTKYVNELYADVFARTYGFNTIGLRYFN 196

Query: 173 VYGPRQDPYGE-AGVVAIFTERMLRGEEVHIFGDGEYVRDYVYVDDVVRANLLA--MEKG 229
           ++G RQDP G  A V+  +   M++ E V+I GDGE  RD+ Y+D+ V+ANLLA   E  
Sbjct: 197 IFGKRQDPDGAYAAVIPKWIASMIKNEPVYINGDGETSRDFCYIDNAVQANLLAATAENT 256

Query: 230 D--NEVFNIGTGRGTTVNQLFKLLKE--------ITGYDKEPVYKPPRKGDVRKSILDYT 279
           D  N+V+N+  G  TT+N+LF  L E        + G+  EP Y+  R GDVR S+ D +
Sbjct: 257 DATNQVYNVAVGDRTTLNELFWHLHENLLPRFAHLQGF--EPNYRDFRAGDVRHSLADMS 314

Query: 280 KAKEKLGWEPKVSLEEGLKLTVEYF 304
           KA++ LG++    + EGL  T+ ++
Sbjct: 315 KAQQLLGYQATHRIGEGLVTTMPWY 339


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: 280
Number of extensions: 17
Number of successful extensions: 6
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: 344
Length adjustment: 28
Effective length of query: 281
Effective length of database: 316
Effective search space:    88796
Effective search space used:    88796
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 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