GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCalpha in Shewanella loihica PV-4

Align phenylpyruvate decarboxylase (EC 4.1.1.43) (characterized)
to candidate 5209454 Shew_1925 3-methyl-2-oxobutanoate dehydrogenase (2-methylpropanoyl-transferring) (RefSeq)

Query= BRENDA::A0A222AKA3
         (368 letters)



>FitnessBrowser__PV4:5209454
          Length = 392

 Score =  178 bits (451), Expect = 3e-49
 Identities = 118/335 (35%), Positives = 164/335 (48%), Gaps = 19/335 (5%)

Query: 37  VPPDRQLLMYRAMVVGRAFNRQATAFSRQGRLAVYPSSRGQEACQVGSALAVRPTDWLFP 96
           +  D    +Y   V  R  + +  A  RQGR++ Y +  G+EA  VGS  A+   D +  
Sbjct: 45  IDQDLAAKIYDTCVFTRVLDERMLAAQRQGRISFYMTCTGEEAAVVGSVAALDQDDVILA 104

Query: 97  TYRESVALLTRGIDPVQVLT--------LFRGDQ---HCGYDPVTEHTAPQCTPLATQCL 145
            YRE  A+  RG    Q +         L +G Q   H G + +   T    +PLATQ  
Sbjct: 105 QYREHAAIRYRGFTTEQFMNQMFSNEKDLGKGRQMPIHYGCEALNYQTIS--SPLATQIP 162

Query: 146 HAAGLADAARMAGDPIVALAYIGDGATSEGDFHEALNYAAVRRAPVVFLVQNNQYAISVP 205
            A G+  + +M G   VA+ Y G+GA SEGDFH  LN AAV  +PV+F  +NN YAIS P
Sbjct: 163 QATGVGYSLKMQGKRNVAICYFGEGAASEGDFHAGLNMAAVLNSPVIFFCRNNGYAISTP 222

Query: 206 LAKQTAARTLADKAAGYGMPGVRIDGNDVLQVYRAVHDAAERARAGHGPTLIEAVTYRID 265
             +Q A   +A +  GYGM  +R+DGND+L V  A   A   A   + P LIEA+TYR+ 
Sbjct: 223 TNEQFAGNGIASRGVGYGMHTIRVDGNDMLAVMAATQQARAYALEHNKPVLIEAMTYRLG 282

Query: 266 AHTNADDDTRYRPAGEADVWAAQDPVDRLERDLLAAGVLDRAAADGIAAAADAFAGELSA 325
           AH+++DD + YR   E   W   DPV R +  L+  G L   A    AA  + +  E+ A
Sbjct: 283 AHSSSDDPSGYRSKDEEAKWQQHDPVKRFKLWLINKGWL---AESDDAALYEKYREEVLA 339

Query: 326 RFSAP---PTGDPMQMFRHVYHHLPPHLREQSERL 357
                   P     ++   V     P L++Q   L
Sbjct: 340 AVKVAEKLPAPKIDEIIEDVLDEPTPRLKQQLTEL 374


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: 321
Number of extensions: 11
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