GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpF in Pseudomonas putida KT2440

Align Aconitate-delta-isomerase 1; Itaconic acid/2-hydroxyparaconate biosynthesis cluster protein ADI1; EC 5.-.-.- (characterized)
to candidate PP_2513 PP_2513 4-oxalomesaconate tautomerase

Query= SwissProt::A0A0U2X0E4
         (443 letters)



>FitnessBrowser__Putida:PP_2513
          Length = 361

 Score =  244 bits (624), Expect = 2e-69
 Identities = 146/326 (44%), Positives = 194/326 (59%), Gaps = 10/326 (3%)

Query: 5   IDTTIYRAGTSRGLYFLASDLPAEPSERDAALISIMGSGHPLQIDGMGGGNSLTSKVAIV 64
           I   + R GTS+G YFL  DLPA    RD  L+++MGS    QIDG+GG +SLTSKVAI+
Sbjct: 6   IPCLLMRGGTSKGAYFLHDDLPAPGPLRDRVLLAVMGSPDARQIDGIGGADSLTSKVAII 65

Query: 65  SASTQRSEFDVDYLFCQVGITERFVDTAPNCGNLMSGVAAFAIERGLVQPHPSDTTCLVR 124
            AS QR + DVDYLF QV + E  VD   NCGN+++GV  FA+ERGLV    + T   VR
Sbjct: 66  RAS-QRDDADVDYLFAQVVVDEARVDYGQNCGNILAGVGPFALERGLVAASGASTP--VR 122

Query: 125 IFNLNSRQASELVIPVYNGRVHY--DDIDDMHMQRPSARVGLRFLDTVGSCTGKLLPTGN 182
           IF  N+ Q +   +P  +G+V Y  D   D    R +A V + F D  G+  G LLPTGN
Sbjct: 123 IFMENTGQIAVAQVPTADGQVEYAGDTRIDGVPGRAAALV-VTFADVAGASCGALLPTGN 181

Query: 183 ASDWIDGLKVSIIDSAVPVVFIRQHDVGITGSEAPATLNANTALLDRLERVRLEAGRRMG 242
           + D ++G++V+ ID+ +PVV +   D+G+TG E   TL A++AL  RLE +RL+ G RM 
Sbjct: 182 SRDCVEGVEVTCIDNGMPVVLLCAEDLGVTGYEPCETLEADSALKTRLEAIRLQLGPRMN 241

Query: 243 LGDVSGSVVPKLSLIGPGTETTTFTARYFTPKACHNAHAVTGAICTAGAAYIDGSVVCEI 302
           LGDVS   VPK+ L+       T   R F P  CH +  V GA+  A A  I+GSV    
Sbjct: 242 LGDVSQRNVPKMCLLSAPRNGGTVNTRSFIPHRCHASIGVFGAVSVATACLIEGSVA--- 298

Query: 303 LSSRASACSASQRRISIEHPSGVLEV 328
               AS     ++R+++EHPSG   V
Sbjct: 299 -QGLASTSGGDRQRLAVEHPSGEFTV 323


Lambda     K      H
   0.318    0.133    0.389 

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: 397
Number of extensions: 12
Number of successful extensions: 4
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: 443
Length of database: 361
Length adjustment: 31
Effective length of query: 412
Effective length of database: 330
Effective search space:   135960
Effective search space used:   135960
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: 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