GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Methylocapsa aurea KYG T

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate WP_036259933.1 DL86_RS07065 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-17424
         (375 letters)



>NCBI__GCF_000746085.1:WP_036259933.1
          Length = 400

 Score =  200 bits (509), Expect = 5e-56
 Identities = 125/371 (33%), Positives = 187/371 (50%), Gaps = 3/371 (0%)

Query: 3   VNDEQQQIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSDT 62
           +++++  +  + RAFAQE L P       D RF +  + +M E GL G  +P+ +GG+  
Sbjct: 24  LSEDESLVRGSARAFAQEVLLPRVTDDYLDERFDRVIMTKMGEFGLLGPTIPQAYGGAGL 83

Query: 63  GYVAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAFA 122
           GYVAY +A  E+   D    + MSV +S+   PI  +G+E Q+ ++L  LA G  +G F 
Sbjct: 84  GYVAYGLAAREVERVDSGYRSAMSVQSSLVMHPIHAYGSEDQRRKYLPRLARGEWIGCFG 143

Query: 123 LTEPQAGSDASSLKTRARLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDPEAGKRGISAF 182
           LTEP+AGSD   ++ RA      Y L G+K +IT+   A + +V+A +   A    I  F
Sbjct: 144 LTEPEAGSDPQGMRARAEKTSRGYRLTGAKTWITNSPLADIFVVWAKS--AAHDNAIRGF 201

Query: 183 IVPTDSPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGGRI 242
           ++     G     +  KL   AS T +I+ D V+VP  N L     G K     L   R 
Sbjct: 202 LLERGMAGLTTPTIGQKLSLRASATGEIIMDGVEVPEQNLL-PNASGLKGPFGCLNRARY 260

Query: 243 GIASQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAAA 302
           GIA   +G A A FE AR Y+ +R+ FG+PL  +Q +  +LADM T+I++  Q  L    
Sbjct: 261 GIAWGTMGAAEACFEAARAYSLDRRQFGRPLAANQLIQKKLADMETEIALGLQAALRIGR 320

Query: 303 LRDAGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYEG 362
           L +  R      S+ K   S  A  +   A    G  G  + F + R   ++     YEG
Sbjct: 321 LFEEDRLTPEAISLVKRNNSGKALDIARMARDMHGANGISAAFHVMRHLANLETVNTYEG 380

Query: 363 TSDIQRMVIAR 373
           TSDI  +++ R
Sbjct: 381 TSDIHALILGR 391


Lambda     K      H
   0.319    0.134    0.382 

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: 348
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: 400
Length adjustment: 30
Effective length of query: 345
Effective length of database: 370
Effective search space:   127650
Effective search space used:   127650
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