GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Pseudomonas stutzeri RCH2

Align acyl-CoA dehydrogenase subunit (EC 1.3.8.4; EC 1.3.8.5) (characterized)
to candidate GFF3761 Psest_3830 Acyl-CoA dehydrogenases

Query= metacyc::MONOMER-11693
         (386 letters)



>FitnessBrowser__psRCH2:GFF3761
          Length = 393

 Score =  181 bits (459), Expect = 3e-50
 Identities = 123/380 (32%), Positives = 192/380 (50%), Gaps = 10/380 (2%)

Query: 1   MDHRLTPELEELRRTVEEFAHDVVAPKIGDFYERHEFPYEIVREMGRMGLFGLPFPEEYG 60
           +D +LT E   ++ +  +FA D +AP++ + +   +    I REMG  GL G   PE YG
Sbjct: 15  LDQQLTEEERMVQGSAAQFAADKLAPRVLEAFRHEQTDPAIFREMGETGLLGATIPEAYG 74

Query: 61  GMGGDYLALGIALEELARVDSSVAITLEAGVSLGAMPIHLFGTDAQKAEWLPRLCSGEIL 120
           G G +Y+  G+   E+ R+DS     +    SL  +PI+ FG +A + ++LP+L SGE +
Sbjct: 75  GSGLNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPIYEFGNEATRQKYLPKLASGEYI 134

Query: 121 GAFGLTEPDGGSDAGATRTTARLDESTNEWVINGTKCFITNSGTDITGLVTVTAVTGRKP 180
           G FGLTEP+ GSD G+  T A+  +    + ++G+K +ITNS      +  V  V  +  
Sbjct: 135 GCFGLTEPNHGSDPGSMVTRAK--KVDGGYRLSGSKMWITNS-----PIADVFVVWAKDD 187

Query: 181 DGKPLISSIIVPSGTPGFTVAAPYSKVGWNASDTRELSFADVRVPAANLLGEQGRGYAQF 240
            G+  I   ++  G  G +    + KVG  AS T E+   +V  P  N   +  RG    
Sbjct: 188 AGE--IRGFVLEKGWEGLSAPTIHGKVGLRASITGEIVMDNVFCPEENAFPDV-RGLKGP 244

Query: 241 LRILDEGRIAISALATGLAQGCVDESVKYAGERHAFGRNIGAYQAIQFKIADMEMKAHMA 300
              L+  R  IS  A G A+ C   + +Y  +R  FGR + A Q IQ K+ADM+ +  +A
Sbjct: 245 FTCLNSARYGISWGALGAAEFCWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLA 304

Query: 301 RVGWRDAASRLVAGEPFKKEAAIAKLYSSTVAVDNAREATQIHGGYGFMNEYPVARMWRD 360
             G          G    +  +I K  S   A+D AR A  + GG G  +E+ VAR   +
Sbjct: 305 LQGCLRLGRMKDEGTAAVEITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVN 364

Query: 361 SKILEIGEGTSEVQRMLIAR 380
            +++   EGT +V  +++ R
Sbjct: 365 LEVVNTYEGTHDVHALILGR 384


Lambda     K      H
   0.318    0.136    0.402 

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: 417
Number of extensions: 25
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: 386
Length of database: 393
Length adjustment: 30
Effective length of query: 356
Effective length of database: 363
Effective search space:   129228
Effective search space used:   129228
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