GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCalpha in Paucidesulfovibrio gracilis DSM 16080

Align phenylpyruvate decarboxylase (EC 4.1.1.43) (characterized)
to candidate WP_078717588.1 B5D49_RS10155 thiamine pyrophosphate-dependent dehydrogenase E1 component subunit alpha

Query= BRENDA::A0A222AKA3
         (368 letters)



>NCBI__GCF_900167125.1:WP_078717588.1
          Length = 319

 Score =  145 bits (365), Expect = 2e-39
 Identities = 109/323 (33%), Positives = 154/323 (47%), Gaps = 25/323 (7%)

Query: 39  PDRQLL--MYRAMVVGRAFNRQATAFSRQGRLAVYPSSR-GQEACQVGSALAVRPTDWLF 95
           PD++ +  MY  M   R F  +   F   G++  +     G+EA   G+   +   D + 
Sbjct: 3   PDKKQMVSMYETMNRIRLFETKLQEFFAAGQIPGFVHLYLGEEAVATGACAGLTNNDKIT 62

Query: 96  PTYRESVALLTRGID-PVQVLTLF-RGDQHCGYDPVTEHTAPQCT-------------PL 140
            T+R    LL +G D  + +  +F R D +C     + H A                 PL
Sbjct: 63  STHRGHGHLLAKGGDLKLMMAEIFGRKDGYCKGKGGSMHIADFDLGILGANGIVGGGGPL 122

Query: 141 ATQCLHAAGLADAARMAGDPIVALAYIGDGATSEGDFHEALNYAAVRRAPVVFLVQNNQY 200
           A      A LA+      D  V + + GDGA+++G   E+LN A+  + P+VF+ +NN Y
Sbjct: 123 AL----GAALANKYEKTDD--VVICFFGDGASNQGTTQESLNMASAWKLPLVFVNENNGY 176

Query: 201 AISVPLAKQTAARTLADKAAGYGMPGVRIDGNDVLQVYRAVHDAAERARAGHGPTLIEAV 260
            IS P  K  A   +AD+AA Y MPGV +DGNDVL V+ AV +A +RAR G GP+L+E  
Sbjct: 177 GISCPQCKSMAVTDIADRAAAYDMPGVVVDGNDVLAVHEAVSEAVKRARNGEGPSLVECK 236

Query: 261 TYRIDAHTNADDDTRYRPAGEADVWAAQDPVDRLERDLLAAGVLDRAAADGIAAAADAFA 320
           TYR   H   D  T YR   E   W A+DP+ R E  L+ +GVL +     I A  +   
Sbjct: 237 TYRWRGHFEGDACT-YRCDEELKEWMAKDPIPRFEEKLVESGVLKKKDLKEIKARIEKEV 295

Query: 321 GELSARFSAPPTGDPMQMFRHVY 343
            E  A     P  DP  +   VY
Sbjct: 296 EEAVAFAEQSPLPDPSVLMDDVY 318


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: 237
Number of extensions: 12
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: 319
Length adjustment: 29
Effective length of query: 339
Effective length of database: 290
Effective search space:    98310
Effective search space used:    98310
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