GapMind for catabolism of small carbon sources

 

Aligments for a candidate for pco in Pseudomonas fluorescens FW300-N2E2

Align acyl-CoA oxidase (EC 1.3.3.6) (characterized)
to candidate Pf6N2E2_1146 Butyryl-CoA dehydrogenase (EC 1.3.99.2)

Query= BRENDA::Q96329
         (436 letters)



>lcl|FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1146 Butyryl-CoA
           dehydrogenase (EC 1.3.99.2)
          Length = 375

 Score =  163 bits (412), Expect = 1e-44
 Identities = 112/374 (29%), Positives = 180/374 (48%), Gaps = 5/374 (1%)

Query: 54  LLTPEEQAIRKKVRECMEKEVAPIMTEYWEKAEFPFHITPKLGAMGVAGGSI-KGYGCPG 112
           L T E+  IR   R+  E+ + P   E+  +  FP     ++  +G  G  + + +G   
Sbjct: 2   LATEEQTQIRDMARQFAEERLKPFAAEWDREHRFPREAIDEMAELGFFGMLVPEQWGGCD 61

Query: 113 LSITANAIATAEIARVDASCSTFILVHSSLGMLTIALCGSEAQKEKYLPSLAQLNTVACW 172
               A A+   EIA  D +CST + VH+S+G + I   G++ QK K+L  LA    +  +
Sbjct: 62  TGYLAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKFGNDEQKAKFLTPLASGAMLGAF 121

Query: 173 ALTEPDNGSDASGLGTTATKVEGGWKINGQKRWIGNSTFADLLIIFA---RNTTTNQING 229
           ALTEP  GSDAS L T A      + +NG K++I +   A ++I+FA    +     I+ 
Sbjct: 122 ALTEPQAGSDASSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISA 181

Query: 230 FIVKKDAPGLKATKIPNKIGLRMVQNGDILLQNVFVPDEDRL-PGVNSFQDTSKVLAVSR 288
           FIV  D+PG    ++ +K+G        IL +++ VP  +RL      ++     L   R
Sbjct: 182 FIVPTDSPGYSVARVEDKLGQHASDTCQILFEDLKVPVGNRLGEEGEGYKIALANLEGGR 241

Query: 289 VMVAWQPIGISMGIYDMCHRYLKERKQFGAPLAAFQLNQQKLVQMLGNVQAMFLMGWRLC 348
           V +A Q +G++   ++    Y +ER  FG P+   Q    +L  M   +     M     
Sbjct: 242 VGIAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIAVARQMVHYAA 301

Query: 349 KLYETGQMTPGQASLGKAWISSKARETASLGRELLGGNGILADFLVAKAFCDLEPIYTYE 408
            L ++GQ    +AS+ K + S  A +  S+  + LGG G L DF + + + D+     YE
Sbjct: 302 ALRDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIYRDVRVCQIYE 361

Query: 409 GTYDINTLVTGREV 422
           GT DI  +V  R +
Sbjct: 362 GTSDIQRMVISRNL 375


Lambda     K      H
   0.319    0.133    0.399 

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: 314
Number of extensions: 17
Number of successful extensions: 3
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: 436
Length of database: 375
Length adjustment: 31
Effective length of query: 405
Effective length of database: 344
Effective search space:   139320
Effective search space used:   139320
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 (21.7 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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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