GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ligU in Pseudomonas putida KT2440

Align (4E)-oxalomesaconate Delta-isomerase; OMA isomerase; 1,3-allylic isomerase LigU; EC 5.3.3.- (characterized)
to candidate PP_2055 PP_2055 putative isomerase

Query= SwissProt::Q0KJL4
         (357 letters)



>FitnessBrowser__Putida:PP_2055
          Length = 359

 Score =  308 bits (789), Expect = 1e-88
 Identities = 166/352 (47%), Positives = 223/352 (63%), Gaps = 5/352 (1%)

Query: 8   MDSAPCMWMRGGTSKGGYFLRADLPADTAARDAFLLAVMGSPDPRQIDGMGGADPLTSKV 67
           M   PC+ MRGGTSKG +F   DLPA+   RD  L+ +MGS    +IDG+GG  P TSKV
Sbjct: 1   MQRIPCVLMRGGTSKGPFFHAWDLPANVVERDELLINLMGSGHELEIDGIGGGSPQTSKV 60

Query: 68  AVVSKSERPGIDVDYLFLQVFVDQAIVTDAQNCGNILAGVGPFAIERGLVAASGDETRVA 127
           A++S S     DVDYLF+QV V Q  V  A NCGN+L  VGPFAIE+GLV     +T V 
Sbjct: 61  AIISPSLHADADVDYLFVQVMVAQRRVDTAPNCGNMLCAVGPFAIEQGLVKGQEGKTLVR 120

Query: 128 IFMENTGQVAVATVRTPGGSVTYAGDAAIDGVPGTHAPIPTEFRDTAGSSCGALLPSGNA 187
           I   NTG    + V TPGG V Y G  AIDGVPGT AP+   F D  GS  G L P+G A
Sbjct: 121 IRNLNTGTFVNSLVETPGGIVRYEGRTAIDGVPGTAAPVHLTFLDAVGSKTGKLFPTGKA 180

Query: 188 VDVVNGLPVTLIDNGMPCVVMKAADVGITGYEDRDSLDANAELKAKIEAIRLAVGELMNL 247
            DV++G+PVT ID  MP +V++A+ +G++G E    LDAN+ L  ++EA+RL  G+ M L
Sbjct: 181 QDVIDGVPVTCIDMAMPMMVVEASQLGVSGSETPAQLDANSALLERLEALRLKAGKAMGL 240

Query: 248 GDVTEKSVPKMMLVAPPRDGGAVCVRSFIPHRAHATIGVLGAVSVATACLIPGSPAAEVA 307
           GDV+   +PK +LV+ PR  G + VR F+PH  H  + + GAV +ATAC+ PG+  A+  
Sbjct: 241 GDVSGMVIPKPVLVSKPRYDGTLQVRYFMPHNCHRALAITGAVGLATACVSPGTVIAD-- 298

Query: 308 VVPEGARK--TLSIEHPTGEMSCVLEVDDA-GNVVSAALLRTARKLMDGVVF 356
           ++ EGA++   + +EHP+G +   L    A G  + A+++RTAR+L  G V+
Sbjct: 299 LLGEGAQQLAQVRLEHPSGGIDVALTRSGAEGQTIQASVVRTARRLFSGFVY 350


Lambda     K      H
   0.318    0.135    0.396 

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: 385
Number of extensions: 18
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: 357
Length of database: 359
Length adjustment: 29
Effective length of query: 328
Effective length of database: 330
Effective search space:   108240
Effective search space used:   108240
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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