GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Snodgrassella alvi wkB2

Align ethanol dehydrogenase / alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate WP_025330295.1 SALWKB2_RS03460 alcohol dehydrogenase AdhP

Query= ecocyc::ADHP-MONOMER
         (336 letters)



>NCBI__GCF_000600005.1:WP_025330295.1
          Length = 337

 Score =  531 bits (1367), Expect = e-155
 Identities = 265/336 (78%), Positives = 290/336 (86%)

Query: 1   MKAAVVTKDHHVDVTYKTLRSLKHGEALLKMECCGVCHTDLHVKNGDFGDKTGVILGHEG 60
           MKAAVVTKD  V +  K +R LK  EALLKMECCGVCHTDLHVKN DFGD TGV LGHEG
Sbjct: 1   MKAAVVTKDKKVAIQDKAVRPLKANEALLKMECCGVCHTDLHVKNADFGDVTGVTLGHEG 60

Query: 61  IGVVAEVGPGVTSLKPGDRASVAWFYEGCGHCEYCNSGNETLCRSVKNAGYSVDGGMAEE 120
           IGVV  VG  VTSLK GDRASVAWF+EGCGHCEYCNSG ET CR VKNAGY+VDGGMAEE
Sbjct: 61  IGVVTAVGEDVTSLKVGDRASVAWFFEGCGHCEYCNSGRETFCREVKNAGYTVDGGMAEE 120

Query: 121 CIVVADYAVKVPDGLDSAAASSITCAGVTTYKAVKLSKIRPGQWIAIYGLGGLGNLALQY 180
           CIVVADYAVKVPDGL S AASSITCAGVTTYKA+K+S I+PGQWIAIYGLGGLGNLALQY
Sbjct: 121 CIVVADYAVKVPDGLSSEAASSITCAGVTTYKAIKVSHIQPGQWIAIYGLGGLGNLALQY 180

Query: 181 AKNVFNAKVIAIDVNDEQLKLATEMGADLAINSHTEDAAKIVQEKTGGAHAAVVTAVAKA 240
           AKNVFNAKVIAIDVN++QL+LA EMGAD+ +N   E   +I+QEK GGA+AAVVTAVAK+
Sbjct: 181 AKNVFNAKVIAIDVNEKQLELAREMGADMTLNPAKEKVEEIIQEKVGGAYAAVVTAVAKS 240

Query: 241 AFNSAVDAVRAGGRVVAVGLPPESMSLDIPRLVLDGIEVVGSLVGTRQDLTEAFQFAAEG 300
           AFNSAV +VRAGGR+VAV LP ++M L+IPRLVLDGIEVVGSLVGTR+DL EAFQF AEG
Sbjct: 241 AFNSAVASVRAGGRIVAVALPVDTMDLNIPRLVLDGIEVVGSLVGTREDLREAFQFGAEG 300

Query: 301 KVVPKVALRPLADINTIFTEMEEGKIRGRMVIDFRH 336
           KVVPKV +RPL DIN IF EM  GK  GRMVIDF++
Sbjct: 301 KVVPKVTMRPLEDINDIFDEMTAGKFTGRMVIDFKN 336


Lambda     K      H
   0.318    0.135    0.395 

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: 403
Number of extensions: 13
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: 336
Length of database: 337
Length adjustment: 28
Effective length of query: 308
Effective length of database: 309
Effective search space:    95172
Effective search space used:    95172
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 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