GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Marinobacter adhaerens HP15

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate GFF2 HP15_2 acyl-CoA dehydrogenase domain protein

Query= CharProtDB::CH_091785
         (379 letters)



>FitnessBrowser__Marino:GFF2
          Length = 389

 Score =  311 bits (797), Expect = 2e-89
 Identities = 159/379 (41%), Positives = 248/379 (65%), Gaps = 1/379 (0%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENVKKMGQYGMMGIPFSKEYG 60
           ++F L    +++R+ +  FA +E+ P A EID    FPM+  +KMG  G++GI  S+EYG
Sbjct: 8   LNFGLGETLDMLREQINGFAASEIAPRAEEIDRNNEFPMDLWRKMGDMGLLGITVSEEYG 67

Query: 61  GAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEKI 120
           G+    L+++IA+EE+S+   + G+   AH++LC + I+ +GTEEQKQKYL  L  GE I
Sbjct: 68  GSDMGYLAHVIAMEEISRASASVGLSYGAHSNLCVNQIHRNGTEEQKQKYLPKLVSGEHI 127

Query: 121 GAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTKG 180
           GA  ++EPNAG+D  + +  A  EGDHY++NG+K++ITNG  A+T+VI+A TD + G++G
Sbjct: 128 GALAMSEPNAGSDVISMKLTAKDEGDHYLLNGNKMWITNGPDANTYVIYAKTDTSAGSRG 187

Query: 181 ISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTLD 240
           ++AFI+E+   GFS  +   KLG+R S+T ELVF+D  VP EN++G  G G  + M  LD
Sbjct: 188 VTAFIVERDAPGFSRHQKLDKLGMRGSNTCELVFQDCKVPKENVLGGVGNGAKVLMSGLD 247

Query: 241 GGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESARYLVY 300
             R+ ++   LGI + A +    Y++ERKQFG+++ +F+ +   +ADM   + +A+  VY
Sbjct: 248 YERLVLSGGPLGIMQAAMDVVVPYIRERKQFGQAIGEFELVQGKVADMYTWMNTAKSYVY 307

Query: 301 KAAYLKQAGLPYT-VDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRDAKIT 359
             A     G   T  DAA A L++A +A  +   A+QL GG GY  +YP  R++RDAK+ 
Sbjct: 308 MVAMSADRGAETTRKDAAGAILYSAEMATKIALDAIQLLGGNGYINEYPTGRLLRDAKLY 367

Query: 360 EIYEGTSEVQKLVISGKIF 378
           EI  GTSE+++++I  +++
Sbjct: 368 EIGAGTSEIRRMLIGRELY 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: 413
Number of extensions: 10
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: 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 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