GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCalpha in Pseudomonas fluorescens FW300-N2E3

Align phenylpyruvate decarboxylase (EC 4.1.1.43) (characterized)
to candidate AO353_19950 AO353_19950 pyruvate dehydrogenase (acetyl-transferring) E1 component subunit alpha

Query= BRENDA::A0A222AKA3
         (368 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_19950
          Length = 327

 Score =  128 bits (322), Expect = 2e-34
 Identities = 98/321 (30%), Positives = 148/321 (46%), Gaps = 15/321 (4%)

Query: 35  AGVPPDRQLLMYRAMVVGRAFNRQATAFSRQGRLAVYPSSR-GQEACQVGSALAVRPTDW 93
           + +P +  L + R M+  R    +A     +G++  +     G+EA  VG+  A+   D 
Sbjct: 4   SSLPKELALGLLRDMLRIRRLEERAGELYGEGKIRGFLHLYIGEEAVAVGALHALAANDA 63

Query: 94  LFPTYRESVALLTRGIDPVQVLTLFRGDQH-CG---------YDPVTEHTAPQCTPLATQ 143
           L  TYRE    L +G+    ++    G Q  C          +D  T             
Sbjct: 64  LVATYREHGHALIKGVPMKTIMAEMYGRQEGCSRGRGGSMHLFDVSTRFFGGNAIVAGGL 123

Query: 144 CLHAAGLADAARMAGDPIVALAYIGDGATSEGDFHEALNYAAVRRAPVVFLVQNNQYAIS 203
            L   GLA A  M G   ++  + G+GA +EG FHE++N AA+ + P++F  +NN YA+ 
Sbjct: 124 PL-TVGLALAEHMQGGSRLSTCFFGEGAMAEGAFHESINLAALWQLPMLFCCENNLYAMG 182

Query: 204 VPLAKQTAARTLADKAAGYGMPGVRIDGNDVLQVYRAVHDAAERARAGHGPTLIEAVTYR 263
             LA+  +   L  KA+ Y +    +DG DV+ VY A   A E  RAG GP  +E  TYR
Sbjct: 183 TALARSQSQTDLCSKASAYKVEARSVDGMDVIAVYEATCLAVEHIRAGRGPYFLEFRTYR 242

Query: 264 IDAHTNADDDTRYRPAGEADVWAAQDPVDRLERDLLAAGVLDRAAADGIAAAADAFAGEL 323
             AH+  D    YR   E + W  + P+      L A G+LD A    I A  DA   E 
Sbjct: 243 FRAHSMFDPQL-YRDKAEVEQWKTRGPIHTYSARLKAEGLLDEAGFQAILAEVDAEV-EA 300

Query: 324 SARFSAPPTGDPMQ-MFRHVY 343
           +  F+   + +P++ + R VY
Sbjct: 301 AVVFADSGSLEPVEDLSRDVY 321


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: 229
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: 368
Length of database: 327
Length adjustment: 29
Effective length of query: 339
Effective length of database: 298
Effective search space:   101022
Effective search space used:   101022
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