GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Sphingomonas koreensis DSMZ 15582

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate Ga0059261_4052 Ga0059261_4052 Acyl-CoA dehydrogenases

Query= CharProtDB::CH_091785
         (379 letters)



>FitnessBrowser__Korea:Ga0059261_4052
          Length = 385

 Score =  285 bits (729), Expect = 1e-81
 Identities = 155/378 (41%), Positives = 232/378 (61%), Gaps = 3/378 (0%)

Query: 1   MDFNLTREQELVRQMVREFAENEVKPIAAEIDETERFPMENV-KKMGQYGMMGIPFSKEY 59
           MDF L+   E++R   + FA+  ++P+AA+ID  + FP + +   MG+ G+ GI   +E+
Sbjct: 6   MDFALSETAEMIRDTTQRFAKERIEPLAAKIDAEDWFPRDELWTAMGELGLHGITVDEEF 65

Query: 60  GGAGGDVLSYIIAVEELSKVCGTTGVILSAHTSLCASLINEHGTEEQKQKYLVPLAKGEK 119
           GG G   L ++IA EE+S+   + G+   AH++LC + I+   +  QK KYL  L  GE 
Sbjct: 66  GGLGLGYLEHVIACEEVSRASASIGLSYGAHSNLCVNQISRWASPAQKAKYLPRLISGEH 125

Query: 120 IGAYGLTEPNAGTDSGAQQTVAVLEGDHYVINGSKIFITNGGVADTFVIFAMTDRTKGTK 179
           +G+  ++E  AG+D  + +  A  +GD YV+NG+K +ITN   ADT V++A T   +G++
Sbjct: 126 VGSLAMSEAGAGSDVVSMKLRAEHKGDRYVLNGTKFWITNAAYADTLVVYAKTG--EGSR 183

Query: 180 GISAFIIEKGFKGFSIGKVEQKLGIRASSTTELVFEDMIVPVENMIGKEGKGFPIAMKTL 239
           GI+ F+IEK   GFSIG+   K+G+R S T ELVF+D  VP EN++G    G  + M  L
Sbjct: 184 GITTFLIEKDMPGFSIGQKIDKMGMRGSPTAELVFDDCEVPEENVMGPLNGGVGVLMSGL 243

Query: 240 DGGRIGIAAQALGIAEGAFNEARAYMKERKQFGRSLDKFQGLAWMMADMDVAIESARYLV 299
           D  R  +A   LGI +   +    Y++ERKQFG+++  FQ +   +ADM VA+ SAR  V
Sbjct: 244 DYERTVLAGIQLGIMQACLDVVLPYLRERKQFGQAIGSFQLMQAKVADMYVALNSARAYV 303

Query: 300 YKAAYLKQAGLPYTVDAARAKLHAANVAMDVTTKAVQLFGGYGYTKDYPVERMMRDAKIT 359
           Y  A    AG     DAA A L A+  A  V  +AVQ  GG GYTKD+PVER +RDAK+ 
Sbjct: 304 YAVAQACDAGKTTRFDAAGAILLASENAFRVAGEAVQALGGAGYTKDWPVERFLRDAKLL 363

Query: 360 EIYEGTSEVQKLVISGKI 377
           +I  GT+E+++++I  ++
Sbjct: 364 DIGAGTNEIRRMLIGREL 381


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: 370
Number of extensions: 9
Number of successful extensions: 3
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: 385
Length adjustment: 30
Effective length of query: 349
Effective length of database: 355
Effective search space:   123895
Effective search space used:   123895
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