GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Sinorhizobium meliloti 1021

Align Sorbitol dehydrogenase; SDH; L-iditol 2-dehydrogenase; Polyol dehydrogenase; Xylitol dehydrogenase; XDH; EC 1.1.1.-; EC 1.1.1.14; EC 1.1.1.9 (characterized)
to candidate SM_b20445 SM_b20445 alcohol dehydrogenase

Query= SwissProt::Q58D31
         (356 letters)



>FitnessBrowser__Smeli:SM_b20445
          Length = 352

 Score =  200 bits (508), Expect = 5e-56
 Identities = 119/327 (36%), Positives = 186/327 (56%), Gaps = 8/327 (2%)

Query: 13  VHGPGDLRLENYPIPEPGPNEVLLKMHSVGICGSDVHYWQHGRIGDFVVKKPMVLGHEAS 72
           ++GP DLRLE   +P PG  EVLLKM + GICGSD+HY+Q G  G   V++P++ GHEAS
Sbjct: 13  LYGPRDLRLEVADVPAPGDGEVLLKMAAGGICGSDLHYYQDGGFGPVRVREPIIPGHEAS 72

Query: 73  GTVVKVGSLVRHLQPGDRVAIEPGAPRETDEFCKIGRYNLSPTIFFCAT----PPDDGNL 128
           G V  +G+ V  L   D VA+ P  P  T  FC  G       + F  +    P   G  
Sbjct: 73  GRVAVLGAGVSGLAIDDLVAVNPSQPCGTCRFCGEGLPVHCLDMRFLGSAMRLPHTQGMF 132

Query: 129 CRFYKHNANFCYKLPDNVTFEEGALIEPLSVGIHACRRAGVTLGNKVLVCGAGPIGLVSL 188
             +    A  C+     V+  E A  EPL+V +HA  +AG   G KVLV GAGPIG + +
Sbjct: 133 RDWLVVPAVQCHPAGSQVSPGEAACAEPLAVCLHAAAQAGEIRGKKVLVTGAGPIGALVV 192

Query: 189 LAAKAMGAAQVVVTDLSASRLSKAKEVGADFILQISNESPQEIAKKVEGLLGSKPEVTIE 248
            AA+  GA ++VVTDL+ + L +AK +GA  I+ +  +     A + +     K  V  E
Sbjct: 193 AAARHAGADEIVVTDLADAALDRAKAMGATRIVNVHRDPAGLAAYEAD---KGKFHVAFE 249

Query: 249 CTGVETSIQAGIYATHSGGTLVLVGLGSEMTSVPLVHAATREVDIKGVFRYCNTWPMAIS 308
           C+  E +++  + A    GT+V VG+  E+T +PL     +E+ + G  R+   + +A++
Sbjct: 250 CSAAEPALRGAVAAVRPRGTIVQVGVTGEIT-LPLHALVGKELRLVGSQRFDGEFALAVA 308

Query: 309 MLASKSVNVKPLVTHRFPLEKALEAFE 335
           +++ + ++V+P+++H+FP+++A+ AFE
Sbjct: 309 LISDRRIDVRPIISHQFPVDEAVRAFE 335


Lambda     K      H
   0.318    0.136    0.410 

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: 341
Number of extensions: 18
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: 356
Length of database: 352
Length adjustment: 29
Effective length of query: 327
Effective length of database: 323
Effective search space:   105621
Effective search space used:   105621
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 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