GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCalpha in Shewanella amazonensis SB2B

Align phenylpyruvate decarboxylase (EC 4.1.1.43) (characterized)
to candidate 6937553 Sama_1709 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (RefSeq)

Query= BRENDA::A0A222AKA3
         (368 letters)



>FitnessBrowser__SB2B:6937553
          Length = 392

 Score =  182 bits (461), Expect = 2e-50
 Identities = 114/329 (34%), Positives = 164/329 (49%), Gaps = 15/329 (4%)

Query: 45  MYRAMVVGRAFNRQATAFSRQGRLAVYPSSRGQEACQVGSALAVRPTDWLFPTYRESVAL 104
           +Y A V  R  + +     RQGR++ Y +  G+EA  +GS  A+   D +   YRE  AL
Sbjct: 53  IYDACVFTRVLDERMLGAQRQGRISFYMTCTGEEAAILGSVAALDEKDVILAQYREHAAL 112

Query: 105 LTRGIDPVQVLT-LFRGDQHCG--------YDPVTEHTAPQCTPLATQCLHAAGLADAAR 155
             RG    Q +  +F  ++  G        Y     H     +PL TQ   A G+  + +
Sbjct: 113 RYRGFTTEQFMNQMFSNEKDLGKGRQMPIHYGTAALHYQTISSPLGTQIPQATGVGYSLK 172

Query: 156 MAGDPIVALAYIGDGATSEGDFHEALNYAAVRRAPVVFLVQNNQYAISVPLAKQTAARTL 215
           M G+  VA+ Y G+GA SEGDFH  +N AAV ++PV+F  +NN YAIS P  +Q A   +
Sbjct: 173 MKGERNVAICYFGEGAASEGDFHAGMNMAAVLKSPVIFFCRNNGYAISTPTEEQFAGNGI 232

Query: 216 ADKAAGYGMPGVRIDGNDVLQVYRAVHDAAERARAGHGPTLIEAVTYRIDAHTNADDDTR 275
           A +  GYGM  +R+DGND+L V  A   A   A   + P LIEA+TYR+ AH+ +DD + 
Sbjct: 233 ASRGVGYGMHTIRVDGNDMLAVLAATQQARAYALEHNAPVLIEAMTYRLGAHSTSDDPSG 292

Query: 276 YRPAGEADVWAAQDPVDRLERDLLAAGVLDRAAADGIAAAADAFAGELSARFSAP---PT 332
           YR   E   W   DPV R +  ++  G L  A  +   A  + +  E+ A        P 
Sbjct: 293 YRSKEEEAKWREHDPVKRFKLWMINKGWLAEANDE---ALYERYREEVLAAVKVAEKIPA 349

Query: 333 GDPMQMFRHVYHHLPPHLREQSERLAAEL 361
               ++   VY    P L++Q E L A +
Sbjct: 350 PRIDEIIEDVYDEPTPLLKKQLESLKAHV 378


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: 328
Number of extensions: 10
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: 392
Length adjustment: 30
Effective length of query: 338
Effective length of database: 362
Effective search space:   122356
Effective search space used:   122356
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: 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