GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Paraburkholderia bryophila 376MFSha3.1

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate H281DRAFT_01054 H281DRAFT_01054 (R,R)-butanediol dehydrogenase / meso-butanediol dehydrogenase / diacetyl reductase

Query= BRENDA::O58389
         (348 letters)



>FitnessBrowser__Burk376:H281DRAFT_01054
          Length = 356

 Score =  158 bits (400), Expect = 2e-43
 Identities = 106/326 (32%), Positives = 165/326 (50%), Gaps = 15/326 (4%)

Query: 23  DVPKP---GPGEVLIKVLATSICGTDLHIYE-------WNEWAQSRIKPPQIMGHEVAGE 72
           +VP P   G  ++++K +   ICGTDLH Y+             +  K PQ++GHE + E
Sbjct: 16  NVPDPSGIGADQMIVKPMWCGICGTDLHEYQAGPIVVPTEPHPLTGAKAPQVLGHEFSAE 75

Query: 73  VVEIGPGVEGIEVGDYVSVETHIVCGKCYACRRGQYHVCQNTKIFGVDTD-GVFAEYAVV 131
           V+E+G  V+ +  GD +SV     CG+CY C RG  H+C      G+  D G  AEY V+
Sbjct: 76  VLEVGRDVKNVRAGDRISVMPLASCGQCYYCVRGMRHLCTKMGCVGLSWDGGGMAEYTVL 135

Query: 132 PAQNIWKNPKSIPPEYATLQEPLGNAVDTVLAGPIS-GKSVLITGAGPLGLLGIAVAKAS 190
              +  + P ++  +   L EP   A+  V  G ++ G SVLITGAGP+G+L      A+
Sbjct: 136 NDYHANRLPDNVSDKQGALIEPAAVALYAVDRGGVTVGSSVLITGAGPIGVLAALACHAA 195

Query: 191 GAYPVIVSEPSDFRRELAKKVG-ADYVINPFEEDVVKEVMDITDGNGVDVFLEFSGAPKA 249
           GA  + VSEP+  R     + G    + +P E ++ + + D+T+G GVDV +E SG   A
Sbjct: 196 GASQIFVSEPNPARAAKMSEFGVTTQIFDPTEGELPERIRDLTEGVGVDVAIECSGNQHA 255

Query: 250 LEQGLQAVTPAGRVSLLGLYPGKVTIDFNNLIIFKALTIYGITGRHLWETWYTVSRLLQS 309
           L   + AV  AG V   GL+ G  T+D     + K + I G T  +    W  +  ++ +
Sbjct: 256 LNACVDAVRSAGAVVQAGLHVGTATVDPMKWSL-KDIHIEG-TWCYPVTIWPRIIGMIAN 313

Query: 310 GKLNLDPIITHKYKGFDKYEEAFELM 335
           GK  ++ +I       D   + F+ +
Sbjct: 314 GKFPVEKLIHDLIDADDVVAKGFDAL 339


Lambda     K      H
   0.318    0.139    0.418 

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: 308
Number of extensions: 17
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: 348
Length of database: 356
Length adjustment: 29
Effective length of query: 319
Effective length of database: 327
Effective search space:   104313
Effective search space used:   104313
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