GapMind for catabolism of small carbon sources

 

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

Align 2-methylbutanoyl-CoA dehydrogenase / butanoyl-CoA dehydrogenase / isobutyryl-CoA dehydrogenase (EC 1.3.8.1; EC 1.3.8.5) (characterized)
to candidate 3608348 Dshi_1750 acyl-CoA dehydrogenase domain protein (RefSeq)

Query= reanno::pseudo3_N2E3:AO353_25680
         (375 letters)



>FitnessBrowser__Dino:3608348
          Length = 381

 Score =  274 bits (700), Expect = 3e-78
 Identities = 156/374 (41%), Positives = 219/374 (58%), Gaps = 5/374 (1%)

Query: 4   TDEQLQISDAARQFAQERLKPFAAEWDREHRFPKEAIGEMAELGFFGMLVPEQWGGCDTG 63
           ++EQ  I D AR F  E + P A  W+++   PK    E+A LGF G+ V E+ GG    
Sbjct: 6   SEEQSAIFDMARDFGAENIAPHALAWEKDGTIPKTLWPELAALGFGGLYVTEESGGSGLS 65

Query: 64  YLAYAMALEEIAAGDGACSTIMSVHNSVGCVPIL-KFGNDDQKERFLKPLASGAMLGAFA 122
            L   +  E ++    + +  +S+HN   C  +L KFG+DD K RFL P  +   + ++ 
Sbjct: 66  RLDATLVFEALSMACPSVAAFLSIHNM--CAAMLDKFGSDDVKARFLPPALTMETVFSYC 123

Query: 123 LTEPQAGSDASSLKTRARLNGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAF 182
           LTEP +GSDA++LKTRA    + Y L G K FI+ G  +   IV A T    G RGIS+ 
Sbjct: 124 LTEPGSGSDAAALKTRAERTNEGYRLTGTKAFISGGGYSDAYIVMARTGED-GPRGISSL 182

Query: 183 IVPTDSPGYKVARVEDKLGQHASDTCQILFEDVQVPVANRLGEEGEGYKIALANLEGGRV 242
           IV   +PG     +EDK+G  A  T Q+  +D  VP AN LGEEG G++ A+  L+GGR+
Sbjct: 183 IVEDGAPGLSFGGLEDKMGWRAQPTRQVQLDDCAVPAANLLGEEGAGFRYAMMGLDGGRL 242

Query: 243 GIASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAA 302
            IA+ S+G A+AA +A   Y  ER +FGKPI + QA+ FRLAD   ++  AR  +  AA 
Sbjct: 243 NIAACSLGAAQAALDATVAYMGERRAFGKPIDQFQALQFRLADAEIELQAARVFLRQAAW 302

Query: 303 LRDSGKP-ALVEASMAKLFASEMAEKVCSTALQTLGGYGYLSDFPLERIYRDVRVCQIYE 361
             D G P A    +MAK F +E   +V    LQ  GGYGYL+D+ +E++ RD+RV QI E
Sbjct: 303 KLDQGAPDATTHCAMAKKFVTEAGSRVADQCLQLHGGYGYLADYGIEKLVRDLRVHQILE 362

Query: 362 GTSDIQRMVISRNL 375
           GT++I R++ +R L
Sbjct: 363 GTNEIMRLLTARAL 376


Lambda     K      H
   0.319    0.134    0.389 

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: 345
Number of extensions: 20
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: 375
Length of database: 381
Length adjustment: 30
Effective length of query: 345
Effective length of database: 351
Effective search space:   121095
Effective search space used:   121095
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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