GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Cronobacter universalis NCTC 9529

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_038858602.1 AFK65_RS19280 L-threonine 3-dehydrogenase

Query= curated2:Q9Z9U1
         (343 letters)



>NCBI__GCF_001277175.1:WP_038858602.1
          Length = 341

 Score =  185 bits (470), Expect = 1e-51
 Identities = 107/345 (31%), Positives = 195/345 (56%), Gaps = 11/345 (3%)

Query: 1   MKALVKTQHGTGHFAVQEKPEPTPGKHQVKIKVKYTGVCGSDIHTYE----GHYPVAAPV 56
           MKAL K Q   G + + + PEP  G + + IK++ T +CG+D+H Y         +  P+
Sbjct: 1   MKALSKLQPAEGIW-MTDVPEPEVGHNDLLIKIRKTAICGTDVHIYNWDDWSQKTIPVPM 59

Query: 57  TLGHEFSGEIVELGEGVTGFNVGDRVTSETTYSICGKCSYCTSGDYNLCSHRKGLGNQQD 116
            +GHE+ GE+V +G+ V GF +GDRV+ E  +  CG C  C  G  +LC +  G+G  + 
Sbjct: 60  VVGHEYVGEVVGIGQEVKGFKIGDRVSGE-GHITCGHCRNCRGGRTHLCRNTVGVGVNRP 118

Query: 117 GSFAKYVIARQESLHHLPAGVDDRSAAMTEPLACTHHAIAKTSINKGDLVVVTGPGPIGL 176
           G FA+Y++    +   +P  + D  A++ +P     H      +  G+ V+V+G GPIG+
Sbjct: 119 GCFAEYLVIPAFNAFKIPDNISDDLASIFDPFGNAVHTALSFDL-VGEDVLVSGAGPIGI 177

Query: 177 LAAQVAKSHGG-TVIITGLSNDQVRLKKAKEVGIDYAIDTQEVDIKELVSELTDGYGADV 235
           +AA VAK  G   V+IT +  ++ RL  A+++G+  A++     ++++++EL    G DV
Sbjct: 178 MAAAVAKHVGARNVVITDV--NEYRLSLARKMGVTRAVNVANESLQDVMNELGMTEGFDV 235

Query: 236 VLECSGAVPAAKQGIDLLRKKGQYAQVGLFAQPEIQFNFEKIIQKEISVVGSRSQKPADW 295
            LE SGA PA +  +D +   G+ A +G+    ++  ++ K+I K + + G   ++  + 
Sbjct: 236 GLEMSGAPPAFRTMLDTMNHGGRIAMLGI-PPSDMSIDWNKVIFKGLFIKGIYGREMFET 294

Query: 296 EPALSLLNEKKVNAKTLVTHEYTISEWDKAYHAIKSGEAIKVLLT 340
              ++ L +  ++   ++TH +TI ++ K + A++SG++ KV+L+
Sbjct: 295 WYKMAALIQSGLDLSPIITHRFTIDDFQKGFDAMRSGQSGKVILS 339


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: 343
Number of extensions: 23
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: 343
Length of database: 341
Length adjustment: 29
Effective length of query: 314
Effective length of database: 312
Effective search space:    97968
Effective search space used:    97968
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