GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Streptococcus massiliensis 4401825

Align Sorbitol dehydrogenase; SDH; EC 1.1.1.-; Glucitol dehydrogenase; L-iditol 2-dehydrogenase; EC 1.1.1.14; Polyol dehydrogenase; Xylitol dehydrogenase; EC 1.1.1.9 (uncharacterized)
to candidate WP_018370771.1 BN415_RS05230 alcohol dehydrogenase AdhP

Query= curated2:Q9Z9U1
         (343 letters)



>NCBI__GCF_000341525.1:WP_018370771.1
          Length = 340

 Score =  137 bits (346), Expect = 3e-37
 Identities = 107/337 (31%), Positives = 159/337 (47%), Gaps = 14/337 (4%)

Query: 1   MKALVKTQHGTGHFAVQEKPEPTPGKHQVKIKVKYTGVCGSDIHTYEGHYPVAAPVTLGH 60
           MKA+V  Q GTG   V +   P      + ++V+Y GVC +D+H   G +       LGH
Sbjct: 1   MKAVVVNQEGTGVEIVDQNIRPIEAGEAL-VEVEYCGVCHTDLHVAHGDFGKVPGRVLGH 59

Query: 61  EFSGEIVELGEGVTGFNVGDRVTSETTYSICGKCSYCTSGDYNLCSHRKGLGNQQDGSFA 120
           E  G + E+   V    VGDRV+    +  CG+C YCT+G   LC   K  G   DG  A
Sbjct: 60  EGIGIVKEVAPDVDSLKVGDRVSIAWFFEGCGRCEYCTTGRETLCRSVKNAGYSVDGGMA 119

Query: 121 KYVIARQESLHHLPAGVDD-RSAAMTEPLACTHHAIAKTSINKGDLVVVTGPGPIGLLAA 179
           +  I   +    +P  +D  +++++T     T+ AI +     G  VVV G G +G LA 
Sbjct: 120 QECIVTADYAVKVPENLDPAQASSITCAGVTTYKAIKEAHAEPGQWVVVYGAGGLGNLAV 179

Query: 180 QVAKS-HGGTVIITGLSNDQVRLKKAKEVGIDYAIDTQEV-DIKELVSELTDGYGADVVL 237
           Q AK      VI   ++ND++ L  AKEVG D+ I+ +EV D+  L+ E T G GA   +
Sbjct: 180 QYAKKVFNAHVIAVDINNDKLEL--AKEVGADFTINGREVEDVPGLIKEHTGG-GAHSAV 236

Query: 238 ECSGAVPAAKQGIDLLRKKGQYAQVGLFAQPEIQFNFEKIIQKEISVVGSRSQKPADWEP 297
             + +  A  Q +D +R  G+   VGL ++  +  +  K +   I V+GS      D E 
Sbjct: 237 VTAVSKVAFNQAVDSVRAGGRVVAVGLPSE-MMDLSIVKTVLDGIQVIGSLVGTRKDLEE 295

Query: 298 ALSLLNEKKVNAKTLVTHEYTISEWDKAYHAIKSGEA 334
           A       +  A+ LV     +   + A H     EA
Sbjct: 296 AF------QFGAEGLVVPVVQLRPVEDACHVFDEMEA 326


Lambda     K      H
   0.315    0.133    0.388 

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: 310
Number of extensions: 24
Number of successful extensions: 4
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: 343
Length of database: 340
Length adjustment: 29
Effective length of query: 314
Effective length of database: 311
Effective search space:    97654
Effective search space used:    97654
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: 42 (22.0 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