GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Beijerinckia indica ATCC 9039

Align Sorbitol dehydrogenase; SDH; (R,R)-butanediol dehydrogenase; L-iditol 2-dehydrogenase; Polyol dehydrogenase; Ribitol dehydrogenase; RDH; Xylitol dehydrogenase; XDH; EC 1.1.1.-; EC 1.1.1.4; EC 1.1.1.14; EC 1.1.1.56; EC 1.1.1.9 (characterized)
to candidate WP_012385190.1 BIND_RS11215 zinc-binding dehydrogenase

Query= SwissProt::Q00796
         (357 letters)



>NCBI__GCF_000019845.1:WP_012385190.1
          Length = 357

 Score =  209 bits (531), Expect = 1e-58
 Identities = 133/357 (37%), Positives = 195/357 (54%), Gaps = 20/357 (5%)

Query: 11  SLVVHGPGDLRLENYPIPEP--GPNEVLLRMHSVGICGSDVHYWEYGRIGNFI------- 61
           +L  H   DLR+E+ P P P  GP EVL++    GICG+D+H +  G I  FI       
Sbjct: 3   ALRFHAAKDLRIEDIPAPPPTPGPGEVLVKNRFCGICGTDLHEYVSGPI--FIPVEPHPF 60

Query: 62  --VKKPMVLGHEASGTVEKVGSSVKHLKPGDRVAIEPGA-PRENDEFCKMGRYNLSPSIF 118
             V  P +LGHE  G V  VG  V   KPGDRV+I+P   PR  D F   G ++LSP + 
Sbjct: 61  TKVSGPQILGHEFGGEVVAVGPGVTSAKPGDRVSIQPLLMPRSGDYFSDRGLFHLSPVLA 120

Query: 119 FCATPPDDGNLCRFYKHNAAFCYKLPDNVTFEEGALIEPLSVGIHACRRGGVTLGHKVLV 178
                   G +  +   N    + +P+ +T EE AL+EP +V ++AC RGGVT G  VLV
Sbjct: 121 LVGLSWQWGGMAEYALVNDYNIHVIPNEMTDEEAALVEPTAVAVYACDRGGVTAGSSVLV 180

Query: 179 CGAGPIGMVTLLVAKAMGAAQVVVTDLSATRLSKAKEIGADLVLQISKES--PQEIARKV 236
            GAGPIGM+TLL A+A GA Q+ ++DL+ TRL  AK I  D++    K+      +  + 
Sbjct: 181 TGAGPIGMLTLLAARAAGATQLFLSDLNETRLQIAKFILPDVITLNPKKDNVGDRVREES 240

Query: 237 EGQLGCKPEVTIECTGAEASIQAGIYATRSGGNLVLVGLGSEMTTVPLLHAAIREVDIKG 296
           EG++GC  +V IEC G E +++A   A R  G +V  GL      +   +   +++DI+G
Sbjct: 241 EGKVGC--DVAIECVGNEHALKACADAVRKQGVVVQTGLHPGENPLNWFNVTFKDIDIRG 298

Query: 297 VFRY-CNTWPVAISMLASKSVNVKPLVTHRFPLEKAL-EAFETFKKGLGLKIMLKCD 351
            + Y  + WP    ++ASK +  + +VT R  L++A+ E F+      G ++ +  D
Sbjct: 299 SWAYPTHYWPRVSRLIASKQLPAQKVVTKRIKLDQAVKEGFDALLDPAGQQLKILID 355


Lambda     K      H
   0.319    0.137    0.415 

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: 366
Number of extensions: 21
Number of successful extensions: 6
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: 357
Length of database: 357
Length adjustment: 29
Effective length of query: 328
Effective length of database: 328
Effective search space:   107584
Effective search space used:   107584
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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.

Links

Downloads

Related tools

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