GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Echinicola vietnamensis KMM 6221, DSM 17526

Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate Echvi_3219 Echvi_3219 Zn-dependent alcohol dehydrogenases

Query= BRENDA::Q8L3C9
         (344 letters)



>FitnessBrowser__Cola:Echvi_3219
          Length = 343

 Score =  531 bits (1368), Expect = e-155
 Identities = 250/341 (73%), Positives = 295/341 (86%)

Query: 1   MLPKTMKAAVIREFGSLLKIEEVEVKRPGRNEILVKVIASGVCHTDLHAVEGDWPVKPKM 60
           MLPKTMKAAV+ EFG  LKIEE+ VK P  N+ILV+V+ASGVCHTDLHA +GDWPVKP++
Sbjct: 1   MLPKTMKAAVVTEFGQPLKIEEIPVKAPNENQILVQVMASGVCHTDLHAADGDWPVKPRL 60

Query: 61  PLIPGHEAVGYVVAVGQEVKNVKEGDAVGVPWLYSACGGCDQCITGWETLCDTQQNGGYS 120
           PLIPGHE +GYV AVG  VKN KEGD VGVPWLYSACG C+ CITGWETLC++Q NGGYS
Sbjct: 61  PLIPGHEGIGYVAAVGSNVKNTKEGDIVGVPWLYSACGHCEHCITGWETLCESQVNGGYS 120

Query: 121 VDGGFAEYVIADARYVGLLPSNVNFMEMAPILCAGVTVYKGLKETEVKPGEWVAISGIGG 180
           VDGG+AEYV+AD  YVG     ++F++MAPILCAGVTVYKGLKETEV+PG+WVAISGIGG
Sbjct: 121 VDGGYAEYVLADPNYVGRFSGAIDFVQMAPILCAGVTVYKGLKETEVRPGQWVAISGIGG 180

Query: 181 LGHVAVQYAKAMGMHVAAIDVADDKLDLAKKLGADLVVNAKNQNPGEFLKKEVGGMHGAL 240
           LGHVAVQYAKAMG+HV A+DV+DDKL+LAKKLGAD VVN KN +     +KE GG+HG L
Sbjct: 181 LGHVAVQYAKAMGLHVLAVDVSDDKLNLAKKLGADRVVNGKNPDEVMNARKETGGVHGVL 240

Query: 241 ITAVSPIAFKQGLETLRRKGTMALNGLPPGNFDLSIFDTVLNRITIRGSIVGTRKDMKEA 300
           +TAVSP+AF+Q L+ LRRKGT+ +NGLPPG+FDL IF+TVLNR T+RGSIVGTRKD++EA
Sbjct: 241 VTAVSPVAFRQALDLLRRKGTLVMNGLPPGSFDLPIFETVLNRYTVRGSIVGTRKDLQEA 300

Query: 301 IEFAVEGKVKATVTPAKLENINEVFDKMKKGQIEGRVVLEI 341
           I+FA+EGKV  TV  A LE+IN +FD+MKKGQIEGR+VL+I
Sbjct: 301 IDFAMEGKVTTTVKSAPLEDINLIFDQMKKGQIEGRMVLDI 341


Lambda     K      H
   0.318    0.137    0.404 

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: 467
Number of extensions: 16
Number of successful extensions: 1
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: 344
Length of database: 343
Length adjustment: 29
Effective length of query: 315
Effective length of database: 314
Effective search space:    98910
Effective search space used:    98910
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 (21.7 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