GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpF in Pseudovibrio axinellae Ad2

Align Aconitate-delta-isomerase 1; Itaconic acid/2-hydroxyparaconate biosynthesis cluster protein ADI1; EC 5.-.-.- (characterized)
to candidate WP_068006840.1 PsAD2_RS13785 4-oxalomesaconate tautomerase

Query= SwissProt::A0A0U2X0E4
         (443 letters)



>NCBI__GCF_001623255.1:WP_068006840.1
          Length = 366

 Score =  238 bits (606), Expect = 3e-67
 Identities = 132/324 (40%), Positives = 188/324 (58%), Gaps = 10/324 (3%)

Query: 11  RAGTSRGLYFLASDLPAEPSERDAALISIMGSGHPLQIDGMGGGNSLTSKVAIVSASTQR 70
           R GTSRG YF   DLP + +  ++AL+S+MG+GHPL IDG+GGG  +T+KVAI+S ST  
Sbjct: 12  RGGTSRGAYFQRKDLPEDETLLESALLSVMGAGHPLNIDGIGGGAEVTTKVAILSPSTDP 71

Query: 71  SEFDVDYLFCQVGITERFVDTAPNCGNLMSGVAAFAIERGLVQPHPSDTTCLVRIFNLNS 130
           S  DVDYLF Q+   +R VD  P CGN+++GV   AIE GLV+     T   +R  N  +
Sbjct: 72  ST-DVDYLFAQIDGHKRIVDFGPTCGNILAGVGPAAIEMGLVEAQNYITHVKIRAVNTGA 130

Query: 131 RQASELVIP----VYNGRVHYDDIDDMHMQRPSARVGLRFLDTVGSCTGKLLPTGNASDW 186
              +++  P     Y G  H D +        +A + + F +  GS TGK+LPTG     
Sbjct: 131 HITAKVKTPDKCVEYEGATHIDGVPGT-----AASIVMEFREVAGSSTGKILPTGQPRTI 185

Query: 187 IDGLKVSIIDSAVPVVFIRQHDVGITGSEAPATLNANTALLDRLERVRLEAGRRMGLGDV 246
           IDGL+VS +D A+P+V +R  D+ I+G E+   L AN  L+ RL  + ++AG+ MGLGD 
Sbjct: 186 IDGLEVSCVDVAMPLVLVRASDINISGYESVDELAANKELMARLASIHIKAGQLMGLGDT 245

Query: 247 SGSVVPKLSLIGPGTETTTFTARYFTPKACHNAHAVTGAICTAGAAYIDGSVVCEILSSR 306
           S  V+PK + +    E    TARYFTP A H + A+TGA C A +   +G++  +  +  
Sbjct: 246 SRQVIPKFAALAMAREGGDITARYFTPWAPHPSMALTGAQCIATSMLYEGTIAVDFYTPP 305

Query: 307 ASACSASQRRISIEHPSGVLEVGL 330
            +        I IEHP G ++V +
Sbjct: 306 VNHSDNQPIAIQIEHPCGHIDVAV 329


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: 378
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: 443
Length of database: 366
Length adjustment: 31
Effective length of query: 412
Effective length of database: 335
Effective search space:   138020
Effective search space used:   138020
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 24 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