GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCalpha in Trichormus variabilis ATCC 29413

Align phenylpyruvate decarboxylase (EC 4.1.1.43) (characterized)
to candidate WP_010996861.1 AVA_RS21680 pyruvate dehydrogenase (acetyl-transferring) E1 component subunit alpha

Query= BRENDA::A0A222AKA3
         (368 letters)



>NCBI__GCF_000204075.1:WP_010996861.1
          Length = 344

 Score =  147 bits (371), Expect = 4e-40
 Identities = 105/329 (31%), Positives = 158/329 (48%), Gaps = 19/329 (5%)

Query: 33  AAAGVPPDRQLLMYRAMVVGRAFNRQATAFSRQGRLAVYPSS-RGQEACQVGSALAVRP- 90
           A A +  +  LL+Y  M +GR F  +      +G++  +     GQEA   G   A+RP 
Sbjct: 13  ANAKITKEEGLLLYEDMTLGRFFEDKCAEMYYRGKMFGFVHLYNGQEAVSTGVIQAMRPG 72

Query: 91  TDWLFPTYRESVALLTRGIDPVQVLT-LFRGDQHC--GYDPVTEHTAPQCTPLATQCLHA 147
            D++  TYR+ V  L+ G+   +V+  LF     C  G        + +   L      A
Sbjct: 73  EDFVSSTYRDHVHALSAGVPAREVMAELFGKATGCSKGRGGSMHMFSAEHGLLGGYAFVA 132

Query: 148 AGLADAARMA----------GDPI---VALAYIGDGATSEGDFHEALNYAAVRRAPVVFL 194
            G+  AA  A          GDP    V   + GDGA + G F E LN AA+ + P++F+
Sbjct: 133 EGIPVAAGAAFQSKYRREVLGDPNADQVTACFFGDGAANNGQFFETLNMAALWKLPIIFV 192

Query: 195 VQNNQYAISVPLAKQTAARTLADKAAGYGMPGVRIDGNDVLQVYRAVHDAAERARAGHGP 254
           V+NN++AI +   + T+   +  KA+ + M GV +DG DVL V     +A  RARAG GP
Sbjct: 193 VENNKWAIGMAHDRATSDPEIYKKASVFNMVGVEVDGMDVLAVRAVAQEAVARARAGEGP 252

Query: 255 TLIEAVTYRIDAHTNADDDTRYRPAGEADVWAAQDPVDRLERDLLAAGVLDRAAADGIAA 314
           TLIEA+TYR   H+ AD D   R   E + W ++DP+ +L   L+   + D A    I  
Sbjct: 253 TLIEALTYRFRGHSLADPD-EMRSKAEKEFWFSRDPIKKLAAYLIEQNLADEAELKAIER 311

Query: 315 AADAFAGELSARFSAPPTGDPMQMFRHVY 343
                  +      + P  DP +++R V+
Sbjct: 312 KIQDVIDDAVKFAESSPEPDPSELYRFVF 340


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: 260
Number of extensions: 10
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: 344
Length adjustment: 29
Effective length of query: 339
Effective length of database: 315
Effective search space:   106785
Effective search space used:   106785
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 Apr 09 2024. 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