GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Shewanella sp. ANA-3

Align UDP-glucose 4-epimerase (EC 5.1.3.2); UDP-N-acetylglucosamine 4-epimerase (EC 5.1.3.7) (characterized)
to candidate 7024172 Shewana3_1379 dTDP-glucose 4,6 dehydratase (RefSeq)

Query= BRENDA::Q9WYX9
         (309 letters)



>FitnessBrowser__ANA3:7024172
          Length = 359

 Score =  140 bits (354), Expect = 3e-38
 Identities = 107/341 (31%), Positives = 169/341 (49%), Gaps = 41/341 (12%)

Query: 1   MNILVTGGAGFIGSHVVDKLIEN-GYGVIVVD------NLSSGKVENLNRNALFYEQSIE 53
           M ILVTGGAGFIGS V+  +I N    VI VD      NL S K+ + N    F +  I 
Sbjct: 1   MKILVTGGAGFIGSAVIRHIIMNTNDSVINVDKLTYAGNLESLKLVSTNPRYNFEQVDIC 60

Query: 54  DEEMMERIFSLHRPEYVFHLAAQASVAISVREPARDAKTNIIGSLVLLEKSIKYGVK--- 110
           D   +ER+FS ++P+ V HLAA++ V  S+  P+   +TNI+G+ +LLE + +Y  +   
Sbjct: 61  DRATLERVFSQYQPDAVMHLAAESHVDRSITGPSDFIQTNIVGTYILLEAARQYWTQLDA 120

Query: 111 ------KFIFSSTGGAIYGE------------NVKVFPTPETEIPHPISPYGIAKYSTEM 152
                 +F   ST   +YG+            N  +    ET    P SPY  +K S++ 
Sbjct: 121 ERKAAFRFHHIST-DEVYGDLPHPDEQEGQAVNQYLPLFTETTPYAPSSPYSASKASSDH 179

Query: 153 YLEFFAREYGLKYTVLRYANVYGPRQDPYGEAGVVAIFTERMLRGEEVHIFGDGEYVRDY 212
            +  + R YG    V   +N YGP   P     ++ +     L G+ + I+G G+ +RD+
Sbjct: 180 LVRAWLRTYGFPTIVTNCSNNYGPYHFP---EKLIPLVILNALEGKSLPIYGKGDQIRDW 236

Query: 213 VYVDDVVRANLLAMEKGD-NEVFNIGTGR--------GTTVNQLFKLLKEITGYDKEPVY 263
           +YV+D  RA    + +G   E +NIG            T  + L  L+ + T Y ++  +
Sbjct: 237 LYVEDHARALYKVVTEGKVGETYNIGGHNEKQNIEVVKTICSILDSLVPKATPYAEQITF 296

Query: 264 KPPRKGDVRKSILDYTKAKEKLGWEPKVSLEEGLKLTVEYF 304
              R G  R+  +D +K   +L W+P+ + E GL+ T+E++
Sbjct: 297 VTDRPGHDRRYAIDASKMSAELNWQPQETFETGLRKTIEWY 337


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: 267
Number of extensions: 14
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: 359
Length adjustment: 28
Effective length of query: 281
Effective length of database: 331
Effective search space:    93011
Effective search space used:    93011
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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