GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Methylocystis bryophila S285

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate WP_085772524.1 B1812_RS16285 isovaleryl-CoA dehydrogenase

Query= CharProtDB::CH_091785
         (379 letters)



>NCBI__GCF_002117405.1:WP_085772524.1
          Length = 389

 Score =  288 bits (737), Expect = 2e-82
 Identities = 153/378 (40%), Positives = 223/378 (58%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENVKKMGQYGMMGIPFSKEYG 60
           MDF L  E E +R+ V EFA  E+ P AA ID    FP +  +KMG  G++G+   +EYG
Sbjct: 8   MDFGLGDEGETLRRSVAEFASREIAPRAARIDADNSFPSDLWRKMGSMGLLGVSVPEEYG 67

Query: 61  GAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEKI 120
           G     L++++A+EE+S+   + G+   AH++LC + I  +G   QK +YL  L  GE +
Sbjct: 68  GVALGYLAHVVAMEEVSRASASVGLSYGAHSNLCVNQIQRNGGRAQKLRYLPKLISGEHV 127

Query: 121 GAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTKG 180
           GA  ++EP AG+D    +  A   GD YV+NG K+++TNG  AD  +++A T    G  G
Sbjct: 128 GALAMSEPAAGSDVVNMRMRAERRGDRYVLNGDKMWVTNGPDADIVIVYAKTSPNAGAHG 187

Query: 181 ISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTLD 240
           I+AFI+E GFKG        KLG+R S+T +L FED  VPV+N++G+   G  + M  LD
Sbjct: 188 ITAFIVEGGFKGLRRMPKLDKLGMRGSNTCQLFFEDCEVPVDNILGEPDCGINVLMSGLD 247

Query: 241 GGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESARYLVY 300
             R+ +A   +GI     +    YM +RKQFGRS+ +F+ +   +ADM  A+ + R  VY
Sbjct: 248 YERVILAGGPIGIMRACLDVVLPYMHDRKQFGRSIGEFEIMQGKLADMYTALSATRAYVY 307

Query: 301 KAAYLKQAGLPYTVDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRDAKITE 360
             A    AG     DAA A L AA  A  +  +A+Q  GG GY  DYP  R++RDAK+ E
Sbjct: 308 AVARACDAGCVSRKDAAGAILFAAERATQMALQAIQCLGGNGYMNDYPTGRLLRDAKLYE 367

Query: 361 IYEGTSEVQKLVISGKIF 378
           I  GTSE+++++I  ++F
Sbjct: 368 IGAGTSEIRRMLIGRELF 385


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: 365
Number of extensions: 12
Number of successful extensions: 1
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: 389
Length adjustment: 30
Effective length of query: 349
Effective length of database: 359
Effective search space:   125291
Effective search space used:   125291
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 Apr 09 2024. 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