GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Tistlia consotensis USBA 355

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate WP_085124268.1 B9O00_RS18920 isovaleryl-CoA dehydrogenase

Query= CharProtDB::CH_091785
         (379 letters)



>NCBI__GCF_900177295.1:WP_085124268.1
          Length = 390

 Score =  306 bits (783), Expect = 8e-88
 Identities = 161/378 (42%), Positives = 233/378 (61%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENVKKMGQYGMMGIPFSKEYG 60
           ++F L  E +L+R  V  F++  + P+A  ID  + FP E   ++G  G+ GI   +EYG
Sbjct: 9   LNFGLGEEADLLRDTVMSFSQERIAPLAERIDREDWFPRELWPQLGALGLHGITVEEEYG 68

Query: 61  GAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEKI 120
           G+G   L + +A+EE+S+   + G+   AH++LC + I  +G+E+QK++YL  L  GE +
Sbjct: 69  GSGLGYLHHCVAMEEVSRASASVGLSYGAHSNLCVNQIRRNGSEDQKRRYLPKLVSGEHV 128

Query: 121 GAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTKG 180
           G+  ++EP AG+D  + +T A   GD +++NG K++ITN   A+T VI+A TD   G +G
Sbjct: 129 GSLAMSEPGAGSDVVSMKTRAEKRGDRWILNGGKMWITNASEAETLVIYAKTDPDAGPRG 188

Query: 181 ISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTLD 240
           I+AFI+EKGFKGFSI +   KLG+R S T ELVFED  VP EN++G+ GKG  + M  LD
Sbjct: 189 ITAFIVEKGFKGFSIAQKLDKLGMRGSPTCELVFEDCEVPEENVLGEVGKGVRVLMSGLD 248

Query: 241 GGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESARYLVY 300
             R  +AA  LGI + A + A  Y+ ERKQFG+ +  FQ +   +ADM     + R  VY
Sbjct: 249 YERAVLAAGPLGIMQAALDVAIPYVHERKQFGQPIGAFQLVQGKLADMYTTANACRAYVY 308

Query: 301 KAAYLKQAGLPYTVDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRDAKITE 360
             A     G     DAA A L+AA  A  V   A+QL GG GY  DYP  R++RDAK+ E
Sbjct: 309 AVAQACDRGETTRKDAAGAILYAAEKATQVALDAIQLLGGNGYINDYPTGRLLRDAKLYE 368

Query: 361 IYEGTSEVQKLVISGKIF 378
           I  GTSE+++ +I  ++F
Sbjct: 369 IGAGTSEIRRWLIGRELF 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: 357
Number of extensions: 10
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: 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 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