GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Halomonas desiderata SP1

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_010628345.1 BZY95_RS09135 acyl-CoA dehydrogenase

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



>NCBI__GCF_002151265.1:WP_010628345.1
          Length = 389

 Score =  216 bits (549), Expect = 1e-60
 Identities = 131/382 (34%), Positives = 206/382 (53%), Gaps = 3/382 (0%)

Query: 6   LNFALGEEIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHG 65
           + F+L ++  AL  +   F+   +A  A + D ++ FP+ + R  GE G LGI   E  G
Sbjct: 1   MEFSLTDDQRALVQAAADFSQAELADHAAEWDATSHFPVDVIRRAGEAGFLGIYIPEERG 60

Query: 66  GAGLGYLAHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISGEHV 125
           G GL  L   +  E++S+   +       H N+    +   G    +  ++ +LISGE +
Sbjct: 61  GLGLSRLDASLIFEQLSQGCIATTAYLTIH-NMVAWMVASWGSDELRETWVERLISGECL 119

Query: 126 GALAMSEPGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTD-PAAGPR 184
           G   ++EPG+GSD  S++ KA + GD YV++GSKM+I+     D+LVV A+T  P +G  
Sbjct: 120 GCYCLTEPGSGSDAASLRTKAVREGDEYVISGSKMFISGAGANDMLVVMARTGAPDSGAG 179

Query: 185 GITAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMSGL 244
           G++A LV     G   G+  +K+G +   T  + F    VP  N+LG  G+G K+ M GL
Sbjct: 180 GVSAILVPADAAGIEYGKNEEKMGWKSQPTRLISFDGVRVPVGNLLGEEGQGFKLAMKGL 239

Query: 245 DYERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYV 304
           D  R+ +++  LG     L +   YL ERKQFG+ +  FQ +Q KLADM   + AAR  V
Sbjct: 240 DGGRLNIASCSLGAAQHALTLARNYLQERKQFGRELAHFQALQFKLADMATELTAARLMV 299

Query: 305 YAVAAACDRGE-TARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKL 363
              A   D+G+  A    A    +A +    +  EA+Q  GG GY  ++P  R++RD ++
Sbjct: 300 RHAAWRLDQGDPEATAYCAMAKRFATDMGFNVCNEALQLHGGYGYLREFPLERMVRDTRV 359

Query: 364 YEIGAGTSEIRRMLIGRELFAE 385
           ++I  GT+EI R+++ R L  +
Sbjct: 360 HQILEGTNEIMRVIVARRLLTD 381


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: 14
Number of successful extensions: 4
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: 389
Length adjustment: 30
Effective length of query: 357
Effective length of database: 359
Effective search space:   128163
Effective search space used:   128163
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.

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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