GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Paludibacter propionicigenes WB4

Align UDP-glucose 4-epimerase (EC 5.1.3.2); UDP-N-acetylglucosamine 4-epimerase (EC 5.1.3.7) (characterized)
to candidate WP_013443943.1 PALPR_RS02055 dTDP-glucose 4,6-dehydratase

Query= BRENDA::Q9WYX9
         (309 letters)



>NCBI__GCF_000183135.1:WP_013443943.1
          Length = 343

 Score =  148 bits (373), Expect = 2e-40
 Identities = 111/329 (33%), Positives = 172/329 (52%), Gaps = 32/329 (9%)

Query: 2   NILVTGGAGFIGSHVVDKLIEN--GYGVIVVDNLS-SGKVENL-----NRNALFYEQSIE 53
           +IL+TGGAGFIGSHVV   +     Y +I +D L+ +G + NL     N N  F +  I 
Sbjct: 6   HILITGGAGFIGSHVVRLFVNKYPEYKIINLDKLTYAGNLANLKDVEDNANYTFIKGDIC 65

Query: 54  DEEMMERIFSLHRPEYVFHLAAQASVAISVREPARDAKTNIIGSLVLLEKSIK-----YG 108
           D + M  +F+ ++ + V HLAA++ V  S+++P   A+TN++G+L LL+ + +     Y 
Sbjct: 66  DFDQMLALFNQYQIDGVIHLAAESHVDRSIKDPFTFAQTNVMGTLSLLQAAKQSWKDAYD 125

Query: 109 VKKFIFSSTGGAIYGE---NVKVFPTPETEIPHPISPYGIAKYSTEMYLEFFAREYGLKY 165
            K F   ST   +YG    + ++F   ET   +P SPY  +K S++ ++  F   YG+  
Sbjct: 126 GKLFYHIST-DEVYGALEMDSELF--TETTNYNPHSPYSASKASSDHFVRAFHDTYGMPV 182

Query: 166 TVLRYANVYGPRQDPYGEAGVVAIFTERMLRGEEVHIFGDGEYVRDYVYVDDVVRANLLA 225
            V   +N YGP Q P     ++ +F   +  G+ + ++G GE VRD++YV D  RA  L 
Sbjct: 183 IVTNCSNNYGPYQFP---EKLIPLFINNIRHGKSLPVYGKGENVRDWLYVVDHARAIDLI 239

Query: 226 MEKGDN-EVFNIGTGRGTT----VNQLFKLLKEITGY-----DKEPVYKPPRKGDVRKSI 275
              G   E +NIG     T    +  L K L  + G+     D    Y   R G   +  
Sbjct: 240 FHTGKTAETYNIGGFNEWTNIDIIRVLIKTLDRLLGHAEGSSDHLITYVTDRAGHDLRYA 299

Query: 276 LDYTKAKEKLGWEPKVSLEEGLKLTVEYF 304
           +D TK K +LGWEP +  EEG++ TV ++
Sbjct: 300 IDSTKLKTELGWEPSLQFEEGIEKTVRWY 328


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: 292
Number of extensions: 9
Number of successful extensions: 4
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 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