GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Dinoroseobacter shibae DFL-12

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate 3608348 Dshi_1750 acyl-CoA dehydrogenase domain protein (RefSeq)

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



>FitnessBrowser__Dino:3608348
          Length = 381

 Score =  239 bits (609), Expect = 1e-67
 Identities = 139/380 (36%), Positives = 210/380 (55%), Gaps = 3/380 (0%)

Query: 6   LNFALGEEIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHG 65
           ++FAL EE  A+    R F +E IAP A   ++    P +LW E+  LG  G+   E  G
Sbjct: 1   MDFALSEEQSAIFDMARDFGAENIAPHALAWEKDGTIPKTLWPELAALGFGGLYVTEESG 60

Query: 66  GAGLGYLAHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISGEHV 125
           G+GL  L   +  E +S A  SV      H N+C   +++ G    K+R+LP  ++ E V
Sbjct: 61  GSGLSRLDATLVFEALSMACPSVAAFLSIH-NMCAAMLDKFGSDDVKARFLPPALTMETV 119

Query: 126 GALAMSEPGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAGPRG 185
            +  ++EPG+GSD  ++K +A++  + Y L G+K +I+ G  +D  +V A+T    GPRG
Sbjct: 120 FSYCLTEPGSGSDAAALKTRAERTNEGYRLTGTKAFISGGGYSDAYIVMARTGED-GPRG 178

Query: 186 ITAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMSGLD 245
           I++ +VE   PG S G   DK+G R   T ++   DC VP  N+LG  G G +  M GLD
Sbjct: 179 ISSLIVEDGAPGLSFGGLEDKMGWRAQPTRQVQLDDCAVPAANLLGEEGAGFRYAMMGLD 238

Query: 246 YERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYVY 305
             R+ ++A  LG   A LD  V Y+ ER+ FG+PI +FQ +Q +LAD  + + AAR ++ 
Sbjct: 239 GGRLNIAACSLGAAQAALDATVAYMGERRAFGKPIDQFQALQFRLADAEIELQAARVFLR 298

Query: 306 AVAAACDRG-ETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKLY 364
             A   D+G   A    A    +  E  + +A + +Q  GG GY  DY   +L+RD +++
Sbjct: 299 QAAWKLDQGAPDATTHCAMAKKFVTEAGSRVADQCLQLHGGYGYLADYGIEKLVRDLRVH 358

Query: 365 EIGAGTSEIRRMLIGRELFA 384
           +I  GT+EI R+L  R L A
Sbjct: 359 QILEGTNEIMRLLTARALLA 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: 284
Number of extensions: 9
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: 381
Length adjustment: 30
Effective length of query: 357
Effective length of database: 351
Effective search space:   125307
Effective search space used:   125307
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