GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Sphingomonas indica Dd16

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 3/3) (EC 1.3.1.109); short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_085219205.1 B9N75_RS13160 isovaleryl-CoA dehydrogenase

Query= BRENDA::Q18AQ1
         (378 letters)



>NCBI__GCF_900177405.1:WP_085219205.1
          Length = 383

 Score =  279 bits (713), Expect = 1e-79
 Identities = 150/360 (41%), Positives = 225/360 (62%), Gaps = 2/360 (0%)

Query: 18  FAENEVKPLATELDEEERFPYETVEKMAKAGMMGIPYPKEYGGEGGDTVGYIMAVEELSR 77
           FAE+ + PLA ++D E+ FP E   +M   G+ GI   +E GG G   + +++A EE++R
Sbjct: 24  FAEDRIAPLAAKIDAEDWFPTELWPEMGALGLHGITVAEEDGGLGLGYLEHVVAQEEVAR 83

Query: 78  VCGTTGVILSAHTSLGSWPIYQYGNEEQKQKFLRPLASGEKLGAFGLTEPNAGTDASGQQ 137
              + G+   AH++L    I ++ N EQK ++L  L SGE +G+  ++E  AG+D    +
Sbjct: 84  ASASIGLSYGAHSNLCVNQIRRWANAEQKARYLPKLISGEHVGSLAMSEAGAGSDVVSMK 143

Query: 138 TTAVLDGDEYILNGSKIFITNAIAGDIYVVMAMTDKSKGNKGISAFIVEKGTPGFSFGVK 197
             A   GD Y+LNG+K +ITNA   D  VV A T   +G++GI+ F++EK   GF+ G K
Sbjct: 144 LKAEKKGDRYVLNGTKFWITNAAYADTLVVYAKT--GEGSRGITTFLIEKDMKGFAIGQK 201

Query: 198 EKKMGIRGSATSELIFEDCRIPKENLLGKEGQGFKIAMSTLDGGRIGIAAQALGLAQGAL 257
             KMG+RGS T+EL+F+DC +P+EN++G E  G  + MS LD  R  +A   LG+ Q  L
Sbjct: 202 LDKMGMRGSPTAELLFDDCEVPEENVMGPENGGVGVLMSGLDYERTVLAGIQLGIMQACL 261

Query: 258 DETVKYVKERVQFGRPLSKFQNTQFQLADMEVKVQAARHLVYQAAINKDLGKPYGVEAAM 317
           D  + +V+ER QFG+ +  FQ  Q ++ADM V + +AR  VY  A   D GK    +AA 
Sbjct: 262 DVVIPFVRERKQFGKAIGSFQLIQAKVADMYVALNSARAYVYAVARACDAGKTTRFDAAG 321

Query: 318 AKLFAAETAMEVTTKAVQLHGGYGYTRDYPVERMMRDAKITEIYEGTSEVQRMVISGKLL 377
           A L A+E A++ + +A+Q  GG GYT+D+PVER  RDAK+ +I  GT+E++RM+I  +L+
Sbjct: 322 AILLASENAVKSSLEAIQALGGAGYTKDWPVERYARDAKLLDIGAGTNEIRRMLIGRELI 381


Lambda     K      H
   0.315    0.133    0.373 

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: 338
Number of extensions: 13
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: 378
Length of database: 383
Length adjustment: 30
Effective length of query: 348
Effective length of database: 353
Effective search space:   122844
Effective search space used:   122844
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: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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