GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Acidovorax caeni R-24608

Align isovaleryl-coenzyme A dehydrogenase; EC 1.3.99.10 (characterized)
to candidate WP_054254997.1 BN2503_RS01970 acyl-CoA dehydrogenase

Query= CharProtDB::CH_122627
         (430 letters)



>NCBI__GCF_001298675.1:WP_054254997.1
          Length = 398

 Score =  205 bits (521), Expect = 2e-57
 Identities = 128/345 (37%), Positives = 184/345 (53%), Gaps = 12/345 (3%)

Query: 82  MWKKLGNAGFLGVTADEEYGGLGMGYQAHCVVMEEISRASGSIALSYAAHSQLCVNQLSL 141
           +++++G  G LG T  E YGG G+ Y ++ ++  EI R         +  S L +  +  
Sbjct: 54  IFREMGALGLLGPTIPEAYGGAGLNYVSYGLIAREIERVDSGYRSMASVQSSLVMVPIHA 113

Query: 142 NGTPEQKARFLPGLLSGEKIGALAMSEHSAGSDVVSMKTSAKEVDGGWVLNGTKMWITNG 201
            GT  QK ++LP L SG  IG   ++E   GSD  SM T A + DGG+ L G+KMWITN 
Sbjct: 114 FGTEAQKQKYLPPLASGAFIGCFGLTEPDHGSDPGSMATRAYKTDGGYRLKGSKMWITNS 173

Query: 202 PDADYIVVYAKTEPEKGSKG-ITAFVVEKTFKGFSCARKLDKLGMRGSNTGELIFEDVFV 260
           P AD  VV+AK   E G+ G I  FV+EK +KG S      K+G+R S TGE++ +DVFV
Sbjct: 174 PVADVFVVWAKEVSESGAVGPIRGFVLEKGWKGLSAPAIHGKVGLRASITGEIVMDDVFV 233

Query: 261 PRENLLGEVNRGVKVLMEGLDLERLVLSAGPLGIMQAALDLVLPYTHVRKQFGAPIAHNQ 320
           P EN   EV RG+K     LD  R  ++ G +G  +        YT  R+QFG P+A NQ
Sbjct: 234 PEENAFPEV-RGLKGPFTCLDSARYGIAWGAMGAAEFCWHTARQYTLDRQQFGRPLAANQ 292

Query: 321 LIQGKLADMHTK--LAASRAYTYATARHIDSHASLGSAAIRTQDCAGAILYAAERATECA 378
           LIQ KLADM T+  L    A  +   +     A  G++ I+  +C         +A + A
Sbjct: 293 LIQKKLADMQTEITLGLQAALRFGRMKDEGIAAVEGTSLIKRNNCG--------KALDIA 344

Query: 379 LDAIQLMGGNGYINEIPAGRLLRDAKLYEIGAGTSEIRRMVIGRA 423
             A  ++GGNG  +E    R L + ++     GT ++  +++GRA
Sbjct: 345 RLARDMLGGNGISDEFGVARHLVNLEVVNTYEGTHDVHALILGRA 389


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: 376
Number of extensions: 22
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: 430
Length of database: 398
Length adjustment: 31
Effective length of query: 399
Effective length of database: 367
Effective search space:   146433
Effective search space used:   146433
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 24 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