GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Dyella japonica UNC79MFTsu3.2

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate N515DRAFT_4257 N515DRAFT_4257 UDP-glucuronate 4-epimerase

Query= BRENDA::P9WN67
         (314 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4257
          Length = 348

 Score =  150 bits (380), Expect = 3e-41
 Identities = 103/335 (30%), Positives = 166/335 (49%), Gaps = 30/335 (8%)

Query: 1   MRALVTGAAGFIGSTLVDRLLADGHSVVGLDN----FATG-RATNLEHLADNSAHVFVEA 55
           M+ LVTG AGFIGS +  +LLA G  V+GLDN    +  G +   L  +     +  V A
Sbjct: 1   MKVLVTGTAGFIGSHVARKLLARGDEVIGLDNLNDYYDVGLKQARLARVQAYPGYTHVHA 60

Query: 56  DIVT-ADLHAILEQHRPEVVFHLAAQIDVRRSVADPQFDAAVNVIGTVRLAEAARQTGVR 114
           D+   A +  +   H+PE V +LAAQ  VR +  +P    + NV G + + E  RQ GV+
Sbjct: 61  DLADRAAVEKLFATHKPERVVNLAAQAGVRYAATNPHVYVSSNVTGFLHILEGCRQHGVQ 120

Query: 115 KIVHTSSGGSIYGTPPEYPTPETAPTD-PASPYAAGKVAGEIYLNTFRHLYGLDCSHIAP 173
            +V  S+  S+YG   + P  E  P + P + YAA K A E   +++ HLYG+  + +  
Sbjct: 121 HLVFASTS-SVYGANRDLPFSEHRPAEHPLTLYAATKKANEQMAHSYAHLYGVPATGLRF 179

Query: 174 ANVYGPRQDPHGEAGVVAIFAQALLSGKPTRVFGDGTNTRDYVFVDDVVDAFVRVSADVG 233
             VYGP   P      + +F QA+L+G+P RVF +G + R + ++DD+V+  VR    V 
Sbjct: 180 FTVYGPWGRPDM---ALFLFTQAILAGEPIRVFNEGRHKRSFTYIDDIVEGVVRALDTVP 236

Query: 234 G---------------GLR----FNIGTGKETSDRQLHSAVAAAVGGPDDPEFHPPRLGD 274
           G               G+     +NIG  +     +    +   +G     E  P + GD
Sbjct: 237 GKDPAWDATQPDPSTSGVAPYRLYNIGNEQPVELLRYIEVLEQYLGRKATMELLPLQAGD 296

Query: 275 LKRSCLDIGLAERVLGWRPQIELADGVRRTVEYFR 309
           +  +  D+      +G+RP++ + +G+   V+++R
Sbjct: 297 VPETEADVSSLVAAVGYRPKVSVEEGIAAFVDWYR 331


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: 289
Number of extensions: 18
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: 348
Length adjustment: 28
Effective length of query: 286
Effective length of database: 320
Effective search space:    91520
Effective search space used:    91520
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