GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Dechlorosoma suillum PS

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate Dsui_0975 Dsui_0975 acyl-CoA dehydrogenase

Query= CharProtDB::CH_091785
         (379 letters)



>FitnessBrowser__PS:Dsui_0975
          Length = 390

 Score =  288 bits (737), Expect = 2e-82
 Identities = 156/381 (40%), Positives = 227/381 (59%), Gaps = 3/381 (0%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENVKKMGQYGMMGIPFSKEYG 60
           +DF      E++R  VR FA  E+ P AA+ID    FP +  +K G  G++G+   +EYG
Sbjct: 6   LDFGHGETIEMLRDTVRAFAAKEIAPRAAQIDRDNEFPADLWQKFGDLGLLGMTAEEEYG 65

Query: 61  GAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEKI 120
           G     L++I+A+EE+S+   + G+   AH++LC + I  +GT  QK KYL  L  G ++
Sbjct: 66  GTAMGYLAHIVAMEEISRASASVGLSYGAHSNLCVNQIRRNGTAAQKAKYLPGLISGTQV 125

Query: 121 GAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTKG 180
           GA  ++EPNAG+D  + +  A  +GD YV+NGSK++ITNGG ADT V++A TD   G KG
Sbjct: 126 GALAMSEPNAGSDVVSMKLKAEKKGDRYVLNGSKMWITNGGDADTLVVYAKTDLNAGAKG 185

Query: 181 ISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTLD 240
           ++AFI+EKGFKGFS G    KLG+R S+T  L F+D  VP EN++G  G G  + M  LD
Sbjct: 186 MTAFIVEKGFKGFSHGTHLDKLGMRGSNTFPLFFDDCEVPEENVLGGVGNGAKVLMSGLD 245

Query: 241 GGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESARYLVY 300
             R  +    LGI     +    Y+ ER+QFG ++ +FQ +   +ADM    ++ R  VY
Sbjct: 246 YERAVLCGGPLGIMAACMDVVLPYLHEREQFGTAIGEFQLMQGKLADMYSTWQATRAYVY 305

Query: 301 ---KAAYLKQAGLPYTVDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRDAK 357
              +A            DAA A L++A  A  +   A+Q  GG GYT +YP  R+ RDAK
Sbjct: 306 AVGQACDRADHARSLRKDAAGAILYSAEKATWMAGDAIQTLGGVGYTNEYPTGRLWRDAK 365

Query: 358 ITEIYEGTSEVQKLVISGKIF 378
           + EI  GTSE+++++I  ++F
Sbjct: 366 LYEIGAGTSEIRRMLIGRELF 386


Lambda     K      H
   0.317    0.135    0.377 

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: 405
Number of extensions: 12
Number of successful extensions: 2
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: 379
Length of database: 390
Length adjustment: 30
Effective length of query: 349
Effective length of database: 360
Effective search space:   125640
Effective search space used:   125640
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: 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