GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pco in Pseudomonas fluorescens GW456-L13

Align acyl-CoA oxidase (EC 1.3.3.6) (characterized)
to candidate PfGW456L13_2983 Butyryl-CoA dehydrogenase (EC 1.3.99.2)

Query= BRENDA::Q96329
         (436 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2983
          Length = 375

 Score =  166 bits (421), Expect = 9e-46
 Identities = 113/370 (30%), Positives = 183/370 (49%), Gaps = 5/370 (1%)

Query: 58  EEQAIRKKVRECMEKEVAPIMTEYWEKAEFPFHITPKLGAMGVAGGSI-KGYGCPGLSIT 116
           ++Q IR   R+  ++ + P   E+  +  FP     ++  +G  G  + + +G       
Sbjct: 6   DQQQIRDMARDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTGYL 65

Query: 117 ANAIATAEIARVDASCSTFILVHSSLGMLTIALCGSEAQKEKYLPSLAQLNTVACWALTE 176
           A A+A  EIA  D +CST + VH+S+G + I   G++ QKE++L  LA    +  +ALTE
Sbjct: 66  AYAMALEEIAAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFALTE 125

Query: 177 PDNGSDASGLGTTATKVEGGWKINGQKRWIGNSTFADLLIIFA---RNTTTNQINGFIVK 233
           P  GSDASGL T A      + +NG K++I +   A ++I+FA    +     I+ FIV 
Sbjct: 126 PQAGSDASGLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFIVP 185

Query: 234 KDAPGLKATKIPNKIGLRMVQNGDILLQNVFVPDEDRL-PGVNSFQDTSKVLAVSRVMVA 292
            D+PG K  ++ +K+G        IL ++V VP  +RL      ++     L   RV +A
Sbjct: 186 TDSPGYKVARVEDKLGQHASDTCQILFEDVKVPLANRLGEEGEGYRIALANLEGGRVGIA 245

Query: 293 WQPIGISMGIYDMCHRYLKERKQFGAPLAAFQLNQQKLVQMLGNVQAMFLMGWRLCKLYE 352
            Q +G++   ++    Y +ER+ FG P+   Q    +L  M   +     M      L +
Sbjct: 246 SQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAALRD 305

Query: 353 TGQMTPGQASLGKAWISSKARETASLGRELLGGNGILADFLVAKAFCDLEPIYTYEGTYD 412
           +G+    +AS+ K + S  A +  S   + LGG G L DF V + + D+     YEGT D
Sbjct: 306 SGKPALVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEGTSD 365

Query: 413 INTLVTGREV 422
           I  +V  R +
Sbjct: 366 IQRMVISRNL 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: 316
Number of extensions: 15
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 (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