GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Halomonas desiderata SP1

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_086509502.1 BZY95_RS08430 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2392
         (383 letters)



>NCBI__GCF_002151265.1:WP_086509502.1
          Length = 385

 Score =  266 bits (680), Expect = 7e-76
 Identities = 148/368 (40%), Positives = 211/368 (57%), Gaps = 1/368 (0%)

Query: 12  MIRDMARDFARREIAPHAQAWEKAGWIDDTLVAQMGELGLLGMVVPEEWGGSYIDYVAYA 71
           +  D  R F  +E+APH +AWE+AG +  +L  Q+GE GLLG+ +PE  GGS  D+    
Sbjct: 11  LFHDTIRRFLEQEVAPHYEAWEEAGEMPRSLWQQLGEAGLLGIDLPEALGGSGADFAIVQ 70

Query: 72  LAVEEISA-GDGATGALMSIHNSVGCGPVLNYGSQAQKDEWLTELASGRAIGCFALTEPQ 130
           LA+EEIS  G G   +  +IH ++    +L+ G+ AQ++ WL  +ASG  IG  A+TEP 
Sbjct: 71  LALEEISRQGFGGLASAYNIHANIVMPYLLHIGTPAQRERWLPAMASGETIGAIAMTEPG 130

Query: 131 AGSEAHNLRTRAELVDGHWVLNGSKQFCSNAKRSKLAIVFAVTDPELGKKGLSAFLVPTD 190
           AGS+   ++TRA   +  W L+GSK F +N + + L IV A TDP  G +G+S FLV T 
Sbjct: 131 AGSDLAAMKTRASRTESGWRLDGSKLFITNGQIADLVIVCAKTDPAAGARGVSLFLVDTT 190

Query: 191 TPGFAVERSEHKMGIRASDTCGVSLSDCRIPEANLLGERGKGLAIALSNLEGGRIGIGAQ 250
             GF+  +   K+G  ASDT  +   D R+PE  LLGE G G A  +  L   R+G+ AQ
Sbjct: 191 LAGFSRGQPIKKIGQHASDTAELFFDDLRLPEEALLGEAGAGFAYLMQELPRERLGVAAQ 250

Query: 251 ALGIARAAFEAALLYARERVQFGKPIAEHQSIANMLADMQTQLNAARLLILHAARLKSAG 310
           ALG    A    L Y RER  FG+ + E Q+    LA+++ Q++  R            G
Sbjct: 251 ALGAMEGALALTLDYVRERRAFGRAVGEFQNTRFTLAEVRAQIDMGRAYFEQCVAKYRQG 310

Query: 311 LPCLSEASQAKLFASEMAEKVCSQAVQIHGGYGYLEDYPVERYYRDARITQIYEGSSEIQ 370
               ++A+  KL  SEM  +     +Q+ GGYGY  +YP+ R+Y DAR+  +Y G+SEI 
Sbjct: 311 EMNGTDAAILKLQLSEMQCRTIDACLQLFGGYGYTREYPISRFYLDARVQTLYAGTSEIM 370

Query: 371 RLLIAREL 378
           + +IAR L
Sbjct: 371 KEVIARSL 378


Lambda     K      H
   0.318    0.133    0.390 

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: 321
Number of extensions: 12
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: 385
Length adjustment: 30
Effective length of query: 353
Effective length of database: 355
Effective search space:   125315
Effective search space used:   125315
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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