GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pco in Dechlorosoma suillum PS

Align acyl-CoA oxidase (EC 1.3.3.6) (characterized)
to candidate Dsui_3369 Dsui_3369 acyl-CoA dehydrogenase

Query= BRENDA::Q96329
         (436 letters)



>FitnessBrowser__PS:Dsui_3369
          Length = 394

 Score =  248 bits (633), Expect = 2e-70
 Identities = 143/386 (37%), Positives = 214/386 (55%), Gaps = 5/386 (1%)

Query: 47  DYYHFNDLLTPEEQAIRKKVRECMEKEVAPIMTEYWEKAEFPFHITPKLGAMGVAGGSIK 106
           D    +D L+ EE+ +R   R+  +  + P + + +   +    I  +LG +G+ G ++ 
Sbjct: 8   DPLQLDDQLSAEERQVRDTARQYSQDRLLPRIVQAFRHEQTDPAIFRELGELGLLGATLD 67

Query: 107 GYGCPGLSITANAIATAEIARVDASCSTFILVHSSLGMLTIALCGSEAQKEKYLPSLAQL 166
           GYGC G S  +  +   EI RVD+   + + V SSL M  I   GSEA KE+ LP +A  
Sbjct: 68  GYGCAGASYVSYGLLAREIERVDSGYRSMVSVQSSLAMYPIHAFGSEALKERLLPKMATG 127

Query: 167 NTVACWALTEPDNGSDASGLGTTATKVEGGWKINGQKRWIGNSTFADLLIIFAR---NTT 223
             + C+ LTEP++GSD   + + A  V GGW++ G K WI NS  AD+ +++A+   +  
Sbjct: 128 ELIGCFGLTEPNHGSDPGSMESRAEAVPGGWELTGAKMWITNSPIADVFVVWAKDGQDED 187

Query: 224 TNQINGFIVKKDAPGLKATKIPNKIGLRMVQNGDILLQNVFVPDEDRLPGVNSFQDTSKV 283
             +I GF+++K   GL A  I  K+GLR    G+I++  VFVP+E+ LP V   +     
Sbjct: 188 GGEIRGFVLEKGMKGLSAPVIQGKMGLRASVTGEIVMDKVFVPEENLLPKVKGLKGPFAC 247

Query: 284 LAVSRVMVAWQPIGISMGIYDMCHRYLKERKQFGAPLAAFQLNQQKLVQMLGNVQAMFLM 343
           L  +R  +AW  +G +   +    +Y  +R QFG PLAA QL Q+KL  M   + A+ L 
Sbjct: 248 LNQARYGIAWGALGAAEACWHAARQYTLDRPQFGRPLAANQLVQKKLADMQTEI-ALGLQ 306

Query: 344 G-WRLCKLYETGQMTPGQASLGKAWISSKARETASLGRELLGGNGILADFLVAKAFCDLE 402
           G  RL +L + G+  P   SL K     KA E A   R++ GGNGI  +F V +   +LE
Sbjct: 307 GCLRLGRLKDEGKDAPEMTSLLKRNSCGKALEIARTARDMHGGNGISDEFHVVRHMLNLE 366

Query: 403 PIYTYEGTYDINTLVTGREVTGIASF 428
            + TYEGT+DI+ L+ GR  TGIA+F
Sbjct: 367 VVNTYEGTHDIHALILGRAQTGIAAF 392


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: 367
Number of extensions: 14
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: 394
Length adjustment: 31
Effective length of query: 405
Effective length of database: 363
Effective search space:   147015
Effective search space used:   147015
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 (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