GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Stutzerimonas stutzeri A1501

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.109); short-chain acyl-CoA dehydrogenase (subunit 1/2) (EC 1.3.8.1) (characterized)
to candidate WP_011911678.1 PST_RS02285 acyl-CoA dehydrogenase

Query= BRENDA::D2RL84
         (383 letters)



>NCBI__GCF_000013785.1:WP_011911678.1
          Length = 393

 Score =  223 bits (569), Expect = 6e-63
 Identities = 133/376 (35%), Positives = 200/376 (53%), Gaps = 5/376 (1%)

Query: 1   MDFNLTEDQQMIKDMAAEFAEKFLAPTVEERDKAHIWDRKLIDKMGEAGFCGICFPEEYG 60
           +D  LTE+++M++  AA+FA   LAP V E  +    D  +  +MGE G  G   PE YG
Sbjct: 15  LDQQLTEEERMVQASAAQFAADKLAPRVLEAFRHERTDPAIFREMGETGLLGATIPEAYG 74

Query: 61  GMGLDVLSYILAVEELSKVDDGTGITLSANVSLCATPIYMFGTEEQKQKYLAPIAEGTHV 120
           G GL+ + Y L   E+ ++D G    +S   SL   PI+ FG E  +QKYL  +A G ++
Sbjct: 75  GSGLNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPIFEFGNEATRQKYLPKLASGEYI 134

Query: 121 GAFGLTEPSAGTDASAQQTTAVLKGDKYILNGSKIFITNGKEADTYVVFAMTDKSQGVHG 180
           G FGLTEP+ G+D  +  T A      Y L+GSK++ITN   AD +VV+A  D  +    
Sbjct: 135 GCFGLTEPNHGSDPGSMVTRAKKVDGGYRLSGSKMWITNSPIADVFVVWAKDDAGE---- 190

Query: 181 ISAFILEKGMPGFRFGKIEDKMGGHTSITAELIFEDCEVPKENLLGKEGEGFKIAMETLD 240
           I  F+LEKG  G     I  K+G   SIT E++ ++   P+EN    +  G K     L+
Sbjct: 191 IRGFVLEKGWEGLSAPTIHGKVGLRASITGEIVMDNVFCPEENAF-PDVRGLKGPFTCLN 249

Query: 241 GGRIGVAAQALGIAEGALAAAVKYSKEREQFGRSISKFQALQFMMADMATKIEAARYLVY 300
             R G++  ALG AE     A +Y  +R+QFGR ++  Q +Q  +ADM T+I  A     
Sbjct: 250 SARYGISWGALGAAEFCWHTARQYVLDRQQFGRPLAANQLIQKKLADMQTEITLALQGCL 309

Query: 301 HAAMLKNEGKPYSEAAAMAKCFASDVAMEVTTDAVQIFGGYGYTVDYPAERYMRNAKITQ 360
               +K+EG    E  ++ K  +   A++V   A  + GG G + ++   R++ N ++  
Sbjct: 310 RLGRMKDEGTAAVEITSLMKRNSCGKALDVARMARDMMGGNGISDEFGVARHLVNLEVVN 369

Query: 361 IYEGTNQVMRIVTSRA 376
            YEGT+ V  ++  RA
Sbjct: 370 TYEGTHDVHALILGRA 385


Lambda     K      H
   0.318    0.134    0.379 

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: 344
Number of extensions: 15
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: 383
Length of database: 393
Length adjustment: 30
Effective length of query: 353
Effective length of database: 363
Effective search space:   128139
Effective search space used:   128139
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