GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Pseudomonas simiae WCS417

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate GFF814 PS417_04135 acyl-CoA dehydrogenase

Query= reanno::Smeli:SM_b21121
         (387 letters)



>FitnessBrowser__WCS417:GFF814
          Length = 378

 Score =  258 bits (660), Expect = 1e-73
 Identities = 150/370 (40%), Positives = 208/370 (56%), Gaps = 1/370 (0%)

Query: 13  EIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHGGAGLGYL 72
           E +  R SVR F  +  AP     ++       LW + GE G+L     E +GG G  +L
Sbjct: 10  EHELFRESVRTFLEKDAAPFHGHWEKQGYIDRRLWNKAGEAGMLCSHLPEEYGGLGADFL 69

Query: 73  AHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISGEHVGALAMSE 132
              V +EEISR   + G+ +  HS++    I   G  A K +YLPKLISGE V A+AM+E
Sbjct: 70  YSAVVIEEISRLGLT-GIGFSLHSDIVAPYILHYGSEALKHKYLPKLISGEMVTAIAMTE 128

Query: 133 PGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAGPRGITAFLVE 192
           PGAGSD+  +K  A   GD YV+NGSK +ITNG  A++++V AKTDP AG +G + FLVE
Sbjct: 129 PGAGSDLQGVKTTAVLDGDEYVINGSKTFITNGYLAELVIVVAKTDPKAGAKGTSLFLVE 188

Query: 193 KAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMSGLDYERVVLS 252
              PGF  G++L+K+GM+  +TSEL F D  VP+EN+LG  G G   LM  L  ER+ ++
Sbjct: 189 ADTPGFDKGKRLEKVGMKAQDTSELFFQDVRVPKENLLGQAGMGFAYLMQELPQERLTVA 248

Query: 253 AGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYVYAVAAACD 312
            G L    A L+  + Y  ERK FG+ I +FQ  + KLA+M   +   R +V    A   
Sbjct: 249 IGALSSAEAALEWTLEYTRERKAFGKAIADFQNTRFKLAEMATEIQIGRVFVDKCMALHL 308

Query: 313 RGETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKLYEIGAGTSE 372
            G+     AA    +A +    +  E +Q  GG G+  +YP  R   DA++  I AGT+E
Sbjct: 309 EGKLDVPTAAMAKYWATDLQCKVLDECVQLHGGYGFMWEYPIARAWADARVQRIYAGTNE 368

Query: 373 IRRMLIGREL 382
           I + +I R L
Sbjct: 369 IMKEIIARAL 378


Lambda     K      H
   0.318    0.135    0.391 

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: 296
Number of extensions: 12
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: 387
Length of database: 378
Length adjustment: 30
Effective length of query: 357
Effective length of database: 348
Effective search space:   124236
Effective search space used:   124236
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