GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Dechlorosoma suillum PS

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate Dsui_3369 Dsui_3369 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-17424
         (375 letters)



>FitnessBrowser__PS:Dsui_3369
          Length = 394

 Score =  194 bits (494), Expect = 3e-54
 Identities = 124/368 (33%), Positives = 189/368 (51%), Gaps = 2/368 (0%)

Query: 6   EQQQIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSDTGYV 65
           E++Q+ D  R ++Q+RL P   Q  +  +       E+ ELGL G  + + +G +   YV
Sbjct: 19  EERQVRDTARQYSQDRLLPRIVQAFRHEQTDPAIFRELGELGLLGATL-DGYGCAGASYV 77

Query: 66  AYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAFALTE 125
           +Y +   EI   D    +++SV +S+   PI  FG+E  KE+ L  +ATG ++G F LTE
Sbjct: 78  SYGLLAREIERVDSGYRSMVSVQSSLAMYPIHAFGSEALKERLLPKMATGELIGCFGLTE 137

Query: 126 PQAGSDASSLKTRARLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDPEAGKRGISAFIVP 185
           P  GSD  S+++RA      + L G+K +IT+   A V +V+A    +     I  F++ 
Sbjct: 138 PNHGSDPGSMESRAEAVPGGWELTGAKMWITNSPIADVFVVWAKDGQDEDGGEIRGFVLE 197

Query: 186 TDSPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGGRIGIA 245
               G     ++ K+G  AS T +IV D V VP  N L  + +G K   A L   R GIA
Sbjct: 198 KGMKGLSAPVIQGKMGLRASVTGEIVMDKVFVPEENLL-PKVKGLKGPFACLNQARYGIA 256

Query: 246 SQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAAALRD 305
             A+G A A +  AR Y  +R  FG+PL  +Q V  +LADM T+I++  Q  L    L+D
Sbjct: 257 WGALGAAEACWHAARQYTLDRPQFGRPLAANQLVQKKLADMQTEIALGLQGCLRLGRLKD 316

Query: 306 AGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYEGTSD 365
            G+ A    S+ K  +   A ++   A    GG G   +F + R   ++ V   YEGT D
Sbjct: 317 EGKDAPEMTSLLKRNSCGKALEIARTARDMHGGNGISDEFHVVRHMLNLEVVNTYEGTHD 376

Query: 366 IQRMVIAR 373
           I  +++ R
Sbjct: 377 IHALILGR 384


Lambda     K      H
   0.319    0.134    0.382 

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: 345
Number of extensions: 26
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: 375
Length of database: 394
Length adjustment: 30
Effective length of query: 345
Effective length of database: 364
Effective search space:   125580
Effective search space used:   125580
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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