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) (characterized)
to candidate Echvi_2328 Echvi_2328 Nucleoside-diphosphate-sugar epimerases

Query= BRENDA::P9WN67
         (314 letters)



>FitnessBrowser__Cola:Echvi_2328
          Length = 346

 Score =  158 bits (399), Expect = 2e-43
 Identities = 113/345 (32%), Positives = 166/345 (48%), Gaps = 40/345 (11%)

Query: 1   MRALVTGAAGFIGSTLVDRLLADGHSVVGLDNFATGRATNL----------------EHL 44
           M+ LVTG AGFIG  L  +LL +GH VVG+D+       NL                EH 
Sbjct: 1   MKFLVTGVAGFIGHGLSKKLLQEGHQVVGIDSINDYYDVNLKLARLKDLGIDDAPISEHQ 60

Query: 45  ----ADNSAHVFVEADIVTAD-LHAILEQHRPEVVFHLAAQIDVRRSVADPQFDAAVNVI 99
                D S   FV+  +   D ++A+ E  R ++V +LAAQ  VR S+ +P+     N++
Sbjct: 61  KVASTDKSCFEFVKMKLEDGDEMNALFEAERFDIVVNLAAQAGVRYSLENPRAYVDANIV 120

Query: 100 GTVRLAEAARQTGVRKIVHTSSGGSIYGTPPEYPTPETAPTD-PASPYAAGKVAGEIYLN 158
           G V L EA R   V+ +V+ SS  S+YG   + P   +   D P S YAA K + E+  +
Sbjct: 121 GFVNLLEACRHHPVKHLVYASS-SSVYGANKKMPFSTSDNVDHPVSLYAASKKSNELMAH 179

Query: 159 TFRHLYGLDCSHIAPANVYGPRQDPHGEAGVVAIFAQALLSGKPTRVFGDGTNTRDYVFV 218
           T+ HLYG+  + +    VYGP   P      + IF +A+L+GKP +VF  G   RD+ +V
Sbjct: 180 TYSHLYGVPTTGLRFFTVYGPWGRPD---MALFIFTKAILNGKPLKVFNYGKMKRDFTYV 236

Query: 219 DDVVDAFVRVS------------ADVGGG--LRFNIGTGKETSDRQLHSAVAAAVGGPDD 264
           DD+V+   R +             D+ G     FNIG  K  +      A+  A G    
Sbjct: 237 DDIVEGVYRTALVPPKGQQEGDKEDLSGAPYRLFNIGNSKSVNLMDFIRAIEKATGKEAV 296

Query: 265 PEFHPPRLGDLKRSCLDIGLAERVLGWRPQIELADGVRRTVEYFR 309
            E  P + GD+  +  D+     V G++P   + DGV   V ++R
Sbjct: 297 LEMLPMQPGDVPATYADVSALSEVTGYKPNTRVEDGVANFVNWYR 341


Lambda     K      H
   0.320    0.137    0.410 

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: 236
Number of extensions: 17
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: 314
Length of database: 346
Length adjustment: 28
Effective length of query: 286
Effective length of database: 318
Effective search space:    90948
Effective search space used:    90948
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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