GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCalpha in Pseudomonas fluorescens FW300-N1B4

Align phenylpyruvate decarboxylase (EC 4.1.1.43) (characterized)
to candidate Pf1N1B4_1020 Branched-chain alpha-keto acid dehydrogenase, E1 component, alpha subunit (EC 1.2.4.4)

Query= BRENDA::A0A222AKA3
         (368 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1020
          Length = 332

 Score =  230 bits (586), Expect = 5e-65
 Identities = 130/320 (40%), Positives = 171/320 (53%), Gaps = 2/320 (0%)

Query: 45  MYRAMVVGRAFNRQATAFSRQGRLAVYPSSRGQEACQVGSALAVRPTDWLFPTYRESVAL 104
           +YR MV+ R F+++A A  R GR+  Y  + GQEA  V     +   D L P YR++   
Sbjct: 4   LYRQMVLTRLFDQKAVALQRTGRIGTYAPTLGQEAIGVAVGSLMHAEDVLIPYYRDTAVQ 63

Query: 105 LTRGIDPVQVLTLFRGDQHCG--YDPVTEHTAPQCTPLATQCLHAAGLADAARMAGDPIV 162
           L RG+   ++L  + GD+      DP      P C P+ATQ LHA G+A A ++ G+  V
Sbjct: 64  LMRGVRMEEILLYWGGDERGSDFADPAVAQDFPICVPIATQALHACGVASAFKIRGEHRV 123

Query: 163 ALAYIGDGATSEGDFHEALNYAAVRRAPVVFLVQNNQYAISVPLAKQTAARTLADKAAGY 222
           A+   GDG TS+GDF EALN A   + PVVF+V NNQ+AISVP   Q  A TLA KA G 
Sbjct: 124 AVTTCGDGGTSKGDFLEALNVAGAWQLPVVFMVNNNQWAISVPRRIQCGAPTLAQKAIGA 183

Query: 223 GMPGVRIDGNDVLQVYRAVHDAAERARAGHGPTLIEAVTYRIDAHTNADDDTRYRPAGEA 282
           G  G ++DGND+L VY  V  A ER R G GP L+E ++YR+  HT ADD TRYR A E 
Sbjct: 184 GFHGEQVDGNDMLAVYDRVQAALERTRHGKGPVLLECLSYRLGDHTTADDATRYRSADEV 243

Query: 283 DVWAAQDPVDRLERDLLAAGVLDRAAADGIAAAADAFAGELSARFSAPPTGDPMQMFRHV 342
                ++P+ RL+R +   GV D      + +            F A     P  +  HV
Sbjct: 244 KQAWLEEPIKRLQRFMAGQGVWDEGREQALISECQGLVQRAVDNFEAAGLQAPESVMDHV 303

Query: 343 YHHLPPHLREQSERLAAELA 362
           Y   P  L EQ E     +A
Sbjct: 304 YAQWPQALAEQREDFLERVA 323


Lambda     K      H
   0.319    0.132    0.395 

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: 279
Number of extensions: 9
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: 368
Length of database: 332
Length adjustment: 29
Effective length of query: 339
Effective length of database: 303
Effective search space:   102717
Effective search space used:   102717
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: 49 (23.5 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