GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Sedimenticola selenatireducens DSM 17993

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_029134232.1 A3GO_RS0115815 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2392
         (383 letters)



>NCBI__GCF_000428045.1:WP_029134232.1
          Length = 397

 Score =  196 bits (498), Expect = 1e-54
 Identities = 118/374 (31%), Positives = 198/374 (52%), Gaps = 6/374 (1%)

Query: 3   DLELSEDQRMIRDMARDFARREIAPHAQAWEKAGWIDDTLVAQMGELGLLGMVVPEEWGG 62
           D +L+E++RM+RD A+ + + ++ P      +    D  ++ +MGELGLLG+ + + +  
Sbjct: 20  DQQLTEEERMVRDTAQKYCQEQLMPRVLEANRHEHFDREIMNEMGELGLLGVTI-DGYDC 78

Query: 63  SYIDYVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGSQAQKDEWLTELASGRAIG 122
           + ++YV+Y L   E+   D    + MS+ +S+   P+  YG++ Q++++L +LA+G  +G
Sbjct: 79  AGLNYVSYGLIAREVERVDSGYRSAMSVQSSLVMHPIYAYGTEEQREKYLPKLATGELVG 138

Query: 123 CFALTEPQAGSEAHNLRTRAELVDGHWVLNGSKQFCSNAKRSKLAIVFAVTDPELGKKGL 182
           CF LTEP  GS+   ++TRA  VDG + L+GSK + +N+  + + IV+A  D  +    +
Sbjct: 139 CFGLTEPDHGSDPAGMKTRARTVDGGYSLSGSKMWITNSPIADVFIVWAKDDEGV----I 194

Query: 183 SAFLVPTDTPGFAVERSEHKMGIRASDTCGVSLSDCRIPEANLLGERGKGLAIALSNLEG 242
             F++     G +  + E K  +RAS T  + + +  +P  NLL    KGLA     L  
Sbjct: 195 RGFILEKGMKGLSAPKIEGKFSLRASITGEIVMDEVFVPAENLL-PNVKGLAGPFGCLNR 253

Query: 243 GRIGIGAQALGIARAAFEAALLYARERVQFGKPIAEHQSIANMLADMQTQLNAARLLILH 302
            R GI    LG A   +  AL Y  +R QFG+P+A +Q I   LA+MQT++       L 
Sbjct: 254 ARYGIAWGVLGAAEDCWHRALTYTLDRKQFGRPLAANQLIQLKLANMQTEITLGLQGCLQ 313

Query: 303 AARLKSAGLPCLSEASQAKLFASEMAEKVCSQAVQIHGGYGYLEDYPVERYYRDARITQI 362
             RL  AG       S  K   +  A  +   A  +HGG G  +++ V R+  +      
Sbjct: 314 LGRLFDAGQAAPEAISLMKRNNAGKALDIARIARDMHGGNGISDEFHVIRHAMNLEAVNT 373

Query: 363 YEGSSEIQRLLIAR 376
           YEG+ ++  L++ R
Sbjct: 374 YEGTHDVHALILGR 387


Lambda     K      H
   0.318    0.133    0.390 

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: 347
Number of extensions: 21
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: 397
Length adjustment: 30
Effective length of query: 353
Effective length of database: 367
Effective search space:   129551
Effective search space used:   129551
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