GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Desulfotalea psychrophila LSv54

Align Putative UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_011187291.1 DP_RS00210 Vi polysaccharide biosynthesis UDP-N-acetylglucosaminuronic acid C-4 epimerase TviC

Query= curated2:Q57664
         (305 letters)



>NCBI__GCF_000025945.1:WP_011187291.1
          Length = 345

 Score =  166 bits (419), Expect = 9e-46
 Identities = 102/318 (32%), Positives = 170/318 (53%), Gaps = 24/318 (7%)

Query: 3   LVTGGAGFIGSHIVDKLIENNYDVIILDNLTTGNKNNINP-----------KAEFVNADI 51
           L+TG AGFIGS++++ L+     V+ LDN  TG ++N++               F+  DI
Sbjct: 19  LITGVAGFIGSNLLETLLGLGQKVVGLDNFVTGYQHNLDEVEGAVTDAQWQNFRFIEGDI 78

Query: 52  RDKDLDEKINFKDVEVVIHQAAQINVRNSVENPVYDGDINVLGTINILEMMRKYDIDKIV 111
              D  ++   + V+ V+ QAA  +V  S+ +P+   + N+ G +N+L   R  ++    
Sbjct: 79  CSLDACQEA-CQGVDYVLQQAALGSVPRSIVDPITTNNTNISGFLNMLVAARDAEVKSFT 137

Query: 112 FASSGGAVYGEPNYLPVDENHPINPLSPYGLSKYVGEEYIKLYNRLYGIEYAILRYSNVY 171
           +A+S  + YG+   LP  E +  NPLSPY ++KYV E Y  ++ R Y  +   LRY N+ 
Sbjct: 138 YAASS-STYGDHPALPKVEENIGNPLSPYAVTKYVNELYASVFARTYSFKTIGLRYFNIL 196

Query: 172 GERQDPKGE-AGVISIFIDKMLKNQSPIIFGDGNQTRDFVYVGDVAKANLMALNWKNE-- 228
           G+RQDP G  A VI ++   M+ +++  I GDG  +RDF ++ +  +AN++A     E  
Sbjct: 197 GKRQDPNGAYAAVIPLWTAAMINDETVFINGDGETSRDFCFIENAVQANILAATATEEAR 256

Query: 229 --IVNIGTGKETSVNELFDIIKHEIGFRG-----EAIYDKPREGEVYRIYLDIKKAES-L 280
             + N+  G  T++NELF++IKH +   G     +  Y   R G+V     D  K +  L
Sbjct: 257 DNVYNVAVGDRTTLNELFNLIKHNLADHGIVYNLDPSYRDFRAGDVRHSQADTTKIKRLL 316

Query: 281 GWKPEIDLKEGIKRVVNW 298
           G+ P+  +  GI++ + W
Sbjct: 317 GYSPQYKIGAGIEKAMGW 334


Lambda     K      H
   0.317    0.140    0.405 

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: 294
Number of extensions: 23
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: 305
Length of database: 345
Length adjustment: 28
Effective length of query: 277
Effective length of database: 317
Effective search space:    87809
Effective search space used:    87809
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