GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Cupriavidus basilensis 4G11

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 RR42_RS09405 RR42_RS09405 butanediol dehydrogenase

Query= curated2:Q9Z9U1
         (343 letters)



>FitnessBrowser__Cup4G11:RR42_RS09405
          Length = 357

 Score =  209 bits (531), Expect = 1e-58
 Identities = 133/335 (39%), Positives = 177/335 (52%), Gaps = 21/335 (6%)

Query: 1   MKALVKTQHGTGHFAVQEKPEPT-PGKHQVKIKVKYTGVCGSDIHTYEGHYPVAAPVT-- 57
           MKA V    G     V+E   P  P +  VKI+V + G+CGSD+H Y    PV  PV   
Sbjct: 1   MKAAV--WRGRHDVRVEEVRVPDKPAEGWVKIRVHWCGICGSDLHEYVAG-PVFIPVDHP 57

Query: 58  -----------LGHEFSGEIVELGEGVTGFNVGDRVTSETTYSICGKCSYCTSGDYNLCS 106
                      LGHEFSGEI ELG GVTGF VG+RVT++     CGKC YCT G YN+C 
Sbjct: 58  HPLTGLKGQCILGHEFSGEIAELGAGVTGFKVGERVTADACQH-CGKCYYCTHGLYNICE 116

Query: 107 HRKGLGNQQDGSFAKYVIARQESLHHLPAGVDDRSAAMTEPLACTHHAIAKTSINKGDLV 166
                G   +G+FA+YV    E L+ LP      + A+ EPLA   HA+ K     G  V
Sbjct: 117 SLAFTGLMNNGAFAEYVNVPAELLYKLPENFPTEAGALIEPLAVGLHAVKKAGNIVGQTV 176

Query: 167 VVTGPGPIGLLAAQVAKSHGGTVIITGLSNDQVRLKKAKEVGIDYAIDTQEVDIKELVSE 226
           VV G G IGL     AK+ G   II  L     R KKA EVG +  ID +E D    V  
Sbjct: 177 VVVGAGTIGLCTIMCAKAAGAGRII-ALEMSSARKKKALEVGANVVIDPKECDAIAQVKA 235

Query: 227 LTDGYGADVVLECSGAVPAAKQGIDLLRKKGQYAQVGLFAQPEIQFNFEKIIQKEISVVG 286
           LT GYGADV  EC G    AK  ID++RK G+   VG+F +P   FNF +I+  E  ++G
Sbjct: 236 LTGGYGADVSFECIGNKATAKLAIDVIRKAGKCVMVGIFEEPS-AFNFFEIVSTEKEIIG 294

Query: 287 SRSQKPADWEPALSLLNEKKVNAKTLVTHEYTISE 321
           S +    ++   +  + + +++ + L+T   ++++
Sbjct: 295 SLAYN-GEFADVIRFIADGRIDVQPLITGRISLAD 328


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: 379
Number of extensions: 19
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: 357
Length adjustment: 29
Effective length of query: 314
Effective length of database: 328
Effective search space:   102992
Effective search space used:   102992
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 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