GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCalpha in Pseudomonas stutzeri RCH2

Align phenylpyruvate decarboxylase (EC 4.1.1.43) (characterized)
to candidate GFF1392 Psest_1429 Pyruvate/2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit

Query= BRENDA::A0A222AKA3
         (368 letters)



>FitnessBrowser__psRCH2:GFF1392
          Length = 329

 Score =  154 bits (390), Expect = 2e-42
 Identities = 103/298 (34%), Positives = 151/298 (50%), Gaps = 26/298 (8%)

Query: 41  RQLLMYRAMVVGRAFNRQATAFSRQGRLAVYPS-----------SRGQEACQVGSALAVR 89
           ++L MY  M+  R           +G+  V+             S GQE C VG    + 
Sbjct: 8   QRLWMYEQMLTSRYMEESIERIYMEGKTPVFNMAKGPIPGEMHLSNGQEPCAVGVCAHLE 67

Query: 90  PTDWLFPTYRESVALLTRGIDPVQVLTLF----------RGDQHCGYDPVTEHTAPQCTP 139
             D +  T+R     + +G+D  +++             RG     +D     +   C+ 
Sbjct: 68  AEDIVTATHRPHHIAVAKGVDLNEMMAEIFGKATGLSGGRGGHMHLFDGRVNFS---CSG 124

Query: 140 LATQCLH-AAGLADAARMAGDPIVALAYIGDGATSEGDFHEALNYAAVRRAPVVFLVQNN 198
           +  + +  A G A + +M G P VA+++IG+GA ++G FHE LN AA+ + PVVF++++N
Sbjct: 125 IIAEGMGPAVGAALSRQMQGKPGVAVSFIGEGAANQGAFHETLNLAALWKLPVVFVIEDN 184

Query: 199 QYAISVPLAKQTAARTLADKAAGYGMPGVRIDGNDVLQVYRAVHDAAERARAGHGPTLIE 258
            + ISV  A  T       +AA YGMPGV ++ ND   V+RA  +A ERARAG GPTLIE
Sbjct: 185 AWGISVAKASATCIAQHHVRAAAYGMPGVFVENNDPDGVFRAAGEAIERARAGGGPTLIE 244

Query: 259 AVTYRIDAHTNADDDTRYRPAGEADVWAAQDPVDRLERDLLAAGVLDRAAADGIAAAA 316
             TYR+  H   D +T YRP GE D    +DP+    + L+  GVL  A A+ IAA A
Sbjct: 245 IETYRLAGHFMGDGET-YRPEGEKDGLIKKDPIPGYRQRLIDEGVLSEAQAEDIAARA 301


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: 281
Number of extensions: 14
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: 329
Length adjustment: 29
Effective length of query: 339
Effective length of database: 300
Effective search space:   101700
Effective search space used:   101700
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