GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Desulfarculus baarsii DSM 2075

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_013258112.1 DEBA_RS06440 acyl-CoA dehydrogenase

Query= reanno::WCS417:GFF2715
         (375 letters)



>NCBI__GCF_000143965.1:WP_013258112.1
          Length = 382

 Score =  336 bits (861), Expect = 7e-97
 Identities = 171/372 (45%), Positives = 247/372 (66%), Gaps = 1/372 (0%)

Query: 5   EEQLQISDAARQFAQERLKPFAAEWDREHRFPKEAIGEMAELGFFGMLVPEQWGGCDTGY 64
           EEQL + + A +FA + LKP AA +D+ H  P E +  + ELGF G+ +PE++GG    Y
Sbjct: 7   EEQLMVKETAARFADDELKPKAAHYDKTHEHPAEFVEALGELGFMGIAIPEEYGGAGMDY 66

Query: 65  LAYAMALEEIAAGDGACSTIMSVHNSVGCVPVLKFGNDQQKEQFLKPLASGAMLGAFALT 124
           ++Y +AL EI+ GD +   IMSV NS+   P+  FG D+QK+ FL P+ASG  LG + LT
Sbjct: 67  VSYVLALSEISRGDASVGVIMSVCNSLYGFPLNSFGTDEQKKAFLTPVASGKKLGCYGLT 126

Query: 125 EPQAGSDASSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPAAGKRGISAFIV 184
           E  AGSD ++++T A L+G+ +VLNG K+FIT+G  A   +V A+TD AAG +GIS+F+V
Sbjct: 127 EAGAGSDPAAMRTTAVLDGNEWVLNGEKKFITNGNVASYAVVAAITDKAAGAKGISSFVV 186

Query: 185 PTD-SPGYSVARVEDKLGQHASDTCQILFEDVKVPVANRLGEEGEGYKIALANLEGGRVG 243
             + + G+SV  +E+K+G  AS T +++FED ++P  N LG+ G G K  L  L  GR+G
Sbjct: 187 DLENTKGFSVGFIEEKMGICASGTSELVFEDARIPKENLLGQLGGGLKQMLMTLNSGRIG 246

Query: 244 IASQAVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303
           I SQA+G+ RA  E A  YA+ERE FGKPI   QA+ ++LAD+AT +  A  ++  AA L
Sbjct: 247 IGSQALGIGRAVLEEAVAYAKEREQFGKPIAAMQAIQWKLADIATHLDAAELLLLRAAWL 306

Query: 304 RDSGKPALVEASMAKLFASEMAEKVCSAALQTLGGYGYLSDFPLERIYRDVRVCQIYEGT 363
            D      ++A+M K++AS+ A       +Q LGGYGY  ++ +ER  RD ++ QIYEGT
Sbjct: 307 EDQHANFEMQAAMGKMYASDAAMAAAIEGVQVLGGYGYCKEYAMERHMRDAKITQIYEGT 366

Query: 364 SDIQRMVISRNL 375
           ++I R+VI+RNL
Sbjct: 367 NEIMRLVIARNL 378


Lambda     K      H
   0.319    0.134    0.387 

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: 385
Number of extensions: 14
Number of successful extensions: 2
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: 382
Length adjustment: 30
Effective length of query: 345
Effective length of database: 352
Effective search space:   121440
Effective search space used:   121440
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 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