GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Dechlorosoma suillum PS

Align isovaleryl-coenzyme A dehydrogenase; EC 1.3.99.10 (characterized)
to candidate Dsui_3369 Dsui_3369 acyl-CoA dehydrogenase

Query= CharProtDB::CH_122627
         (430 letters)



>FitnessBrowser__PS:Dsui_3369
          Length = 394

 Score =  189 bits (480), Expect = 1e-52
 Identities = 128/376 (34%), Positives = 194/376 (51%), Gaps = 16/376 (4%)

Query: 52  ELRESVQEFTSR--ISTVVAARTDAQNEFPAEMWKKLGNAGFLGVTADEEYGGLGMGYQA 109
           ++R++ ++++    +  +V A    Q + PA ++++LG  G LG T D  YG  G  Y +
Sbjct: 22  QVRDTARQYSQDRLLPRIVQAFRHEQTD-PA-IFRELGELGLLGATLDG-YGCAGASYVS 78

Query: 110 HCVVMEEISRASGSIALSYAAHSQLCVNQLSLNGTPEQKARFLPGLLSGEKIGALAMSEH 169
           + ++  EI R         +  S L +  +   G+   K R LP + +GE IG   ++E 
Sbjct: 79  YGLLAREIERVDSGYRSMVSVQSSLAMYPIHAFGSEALKERLLPKMATGELIGCFGLTEP 138

Query: 170 SAGSDVVSMKTSAKEVDGGWVLNGTKMWITNGPDADYIVVYAKTEPEKGSKGITAFVVEK 229
           + GSD  SM++ A+ V GGW L G KMWITN P AD  VV+AK   ++    I  FV+EK
Sbjct: 139 NHGSDPGSMESRAEAVPGGWELTGAKMWITNSPIADVFVVWAKDGQDEDGGEIRGFVLEK 198

Query: 230 TFKGFSCARKLDKLGMRGSNTGELIFEDVFVPRENLLGEVNRGVKVLMEGLDLERLVLSA 289
             KG S      K+G+R S TGE++ + VFVP ENLL +V +G+K     L+  R  ++ 
Sbjct: 199 GMKGLSAPVIQGKMGLRASVTGEIVMDKVFVPEENLLPKV-KGLKGPFACLNQARYGIAW 257

Query: 290 GPLGIMQAALDLVLPYTHVRKQFGAPIAHNQLIQGKLADMHTKLAASRAYTYATARHID- 348
           G LG  +A       YT  R QFG P+A NQL+Q KLADM T++A          R  D 
Sbjct: 258 GALGAAEACWHAARQYTLDRPQFGRPLAANQLVQKKLADMQTEIALGLQGCLRLGRLKDE 317

Query: 349 -SHASLGSAAIRTQDCAGAILYAAERATECALDAIQLMGGNGYINEIPAGRLLRDAKLYE 407
              A   ++ ++   C         +A E A  A  + GGNG  +E    R + + ++  
Sbjct: 318 GKDAPEMTSLLKRNSCG--------KALEIARTARDMHGGNGISDEFHVVRHMLNLEVVN 369

Query: 408 IGAGTSEIRRMVIGRA 423
              GT +I  +++GRA
Sbjct: 370 TYEGTHDIHALILGRA 385


Lambda     K      H
   0.319    0.134    0.389 

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: 365
Number of extensions: 19
Number of successful extensions: 3
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: 430
Length of database: 394
Length adjustment: 31
Effective length of query: 399
Effective length of database: 363
Effective search space:   144837
Effective search space used:   144837
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: 50 (23.9 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