GapMind for catabolism of small carbon sources

 

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

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate 3607424 Dshi_0838 acyl-CoA dehydrogenase domain protein (RefSeq)

Query= reanno::pseudo3_N2E3:AO353_25670
         (383 letters)



>FitnessBrowser__Dino:3607424
          Length = 382

 Score =  248 bits (633), Expect = 2e-70
 Identities = 140/376 (37%), Positives = 215/376 (57%), Gaps = 3/376 (0%)

Query: 6   LTEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDALVAKMGELGLLGMVVPEEWGGTYV 65
           +T+E  M+ +M R+F   E APH + W   G +D  +  + GELGLL   VPE +GG   
Sbjct: 7   MTDEHRMLAEMTRNFITTEWAPHFERWRDQGEMDREIWQQAGELGLLCPSVPEAYGGPGG 66

Query: 66  DYVAYALAVEEISAGD-GATGALMSIHNSVGCGPVLNYGTEEQKQTWLADLASGQAIGCF 124
           D+   A  + EI+  +  A GA   IH+ +    +L YG+EEQKQ WL  + SG+ +G  
Sbjct: 67  DFGHEAAILIEIARANLSAWGAGHGIHSGIVAHYILAYGSEEQKQKWLPKMVSGEMVGAL 126

Query: 125 CLTEPQAGSEAHNLRTRAELRDGQWVINGAKQFVSNGRRAKLAIVFAVTDPDLGKKGLSA 184
            +TEP AGS+   ++TRA      + ++G+K F++NG+ A L +V A TDP  G KG+S 
Sbjct: 127 AMTEPGAGSDLQGIKTRAVKDGNGYRLSGSKIFITNGQHANLIVVAAKTDPSAGAKGVSL 186

Query: 185 FLVPTD-TPGFIVDRSEHKMGIRASDTCAVTLNNCTIPEANLLG-ERGKGLAIALSNLEG 242
            ++ T+   GF   R+ HK+G+ ASDT  +  +N  IP  NLLG E GKG    ++ L  
Sbjct: 187 VVLETEGAEGFSRGRNLHKVGMHASDTSELFFDNVAIPPENLLGGEVGKGFYQMMTQLPQ 246

Query: 243 GRIGIAAQALGIARAAFEAALAYARDRVQFDKPIIEHQSVANMLADMHTRLNAARLLILH 302
            R+ IAA A+G    A E  +AYA++R  F  PI++ Q+    LA+  T+   AR  +  
Sbjct: 247 ERLIIAAGAVGAMEGAVERTVAYAKERQAFGGPILQFQNTRFKLAECQTKTTVARAFLNE 306

Query: 303 AARLRSAGKPCLSEASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVERYYRDARITQI 362
                  GK  + +A+ AK + ++   +V    +Q+HGGYGY+ +Y + + + DAR+ +I
Sbjct: 307 CMAEHLEGKLSVEKAAMAKYWITDTQGEVIDECVQLHGGYGYMAEYDIAQMWSDARVQRI 366

Query: 363 YEGSSEIQRMVIAREL 378
           Y G++EI + +I R L
Sbjct: 367 YGGTNEIMKELIGRAL 382


Lambda     K      H
   0.319    0.134    0.394 

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: 363
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: 383
Length of database: 382
Length adjustment: 30
Effective length of query: 353
Effective length of database: 352
Effective search space:   124256
Effective search space used:   124256
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