GapMind for catabolism of small carbon sources

 

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

Align D-threo-aldose 1-dehydrogenase; L-fucose dehydrogenase; EC 1.1.1.122 (characterized)
to candidate H281DRAFT_02575 H281DRAFT_02575 D-threo-aldose 1-dehydrogenase

Query= SwissProt::Q52472
         (329 letters)



>FitnessBrowser__Burk376:H281DRAFT_02575
          Length = 325

 Score =  168 bits (426), Expect = 1e-46
 Identities = 109/315 (34%), Positives = 166/315 (52%), Gaps = 26/315 (8%)

Query: 15  IPALGYGAANVGNLFRALSDDEAWAVLEAAWDAGIRYYDTAPHYGLGLSEKRLGAFLQTK 74
           +P +G GA   G+L  A  +   + ++ AAW +G+RY+DT+  Y  G SE+RLGA L   
Sbjct: 14  LPRVGVGA---GSLANAAGEQAFFNMIHAAWASGVRYFDTSAAYLGGESEQRLGAALAAC 70

Query: 75  PRDEFVVSTKAGRLL-RPNPERRPSGLDTDNDFHVPDDLRREWDFTEQGIRASIAESQER 133
           PR+E  VSTK GR L +P     P G    ++F++        D+T      S+  S  R
Sbjct: 71  PREELYVSTKLGRYLSQPGASSLPGG----SNFYL--------DYTYDTTLRSVERSLSR 118

Query: 134 LGLDRIDLLYLHDPE--------RHDLDLALASAFPALEKVRAEGVVKAIGIGSMVSDAL 185
           L +DR+D +++HD +        R +L  A+  AFPAL++++ E VV AIG+ SM   A 
Sbjct: 119 LKVDRLDAVFIHDLDPGFAQAAYREELKTAVEGAFPALQRLKDEKVVGAIGVASMDWQAC 178

Query: 186 TRAVREADLDLIMVAGRYTLLEQPAATEVLPACAENATGIVAASVFNSGLLAQSEPKRDG 245
                 AD+D++M AG Y+LL +  +T +L  C E     +AAS FNSG+LA    + D 
Sbjct: 179 LDFAEMADVDVVMPAGEYSLL-RTRSTALLEHCVEKGIAWIAASPFNSGILATGS-RPDA 236

Query: 246 RYEYGQLPDELWDRLVRIAAICRNHDVPLPAAAIQFPLQSALVRSVVVGGSRPAQLTQNA 305
            Y       ++  +   +  ICR HDVPL  AA+ FPL+   V ++V G     +  ++ 
Sbjct: 237 FYNMRPATRQVLSQTEGLECICRRHDVPLATAALLFPLRHPAVSTIVFGAKTSDEFNESF 296

Query: 306 EYAALEIPAGLWAEL 320
              +  +P   W E+
Sbjct: 297 ARLSGNLPDQFWHEM 311


Lambda     K      H
   0.318    0.135    0.395 

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: 271
Number of extensions: 16
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: 329
Length of database: 325
Length adjustment: 28
Effective length of query: 301
Effective length of database: 297
Effective search space:    89397
Effective search space used:    89397
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: 48 (23.1 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