GapMind for catabolism of small carbon sources

 

Alignments for a candidate for LRA3 in Pseudomonas fluorescens FW300-N2E2

Align L-fuconate dehydratase; L-rhamnonate dehydratase (EC 4.2.1.68; EC 4.2.1.90) (characterized)
to candidate Pf6N2E2_860 Altronate dehydratase (EC 4.2.1.7)

Query= reanno::BFirm:BPHYT_RS34230
         (431 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_860
          Length = 515

 Score =  206 bits (524), Expect = 1e-57
 Identities = 140/414 (33%), Positives = 205/414 (49%), Gaps = 32/414 (7%)

Query: 5   AQQPTLEGYLRGDGRKGIRNVVAVAYLVECAHHVAREIVTQFREPLDAFDDPSAEREPP- 63
           ++ P+  G +R DGR   RN + +   V C+  VAR I   FR  ++    P+A +  P 
Sbjct: 109 SEAPSFMGIVRPDGRVATRNYIGILTSVNCSATVARAIADHFRRDIN----PAALQAYPN 164

Query: 64  ----VHLIGFPGCY--PNGYAEKMLERL----TTHPNVGAVLFVSLGCESMNKHYLVDVV 113
               V L    GC   P G    ML R      TH N  AVL + LGCE+     L+   
Sbjct: 165 VDGVVALTHSAGCAVDPAGDGLSMLRRTLAGYATHANFAAVLVIGLGCETNQIDSLLTTQ 224

Query: 114 RAS-GRPVEVLTIQEKGGTRSTIQYGVDWIRGAREQLAAQQKVPMALSELVIGTICGGSD 172
             +    +    IQ+ GGT   I  G+D ++    +    Q+ P++   L +G  CGGSD
Sbjct: 225 GLTRSNTLRTFNIQDSGGTSKAIASGIDHVKQLLGEANQIQREPVSARHLTVGLQCGGSD 284

Query: 173 GTSGITANPAVGRAFDHLIDAGATCIFEETGELVGCEFHMKTRAARPALGDEIVACVAKA 232
           G SGITANPA+G A D L+  G T I  ET E+ G E  +  RA    +G++++A +   
Sbjct: 285 GYSGITANPALGNAVDRLVACGGTAILSETPEIYGAEHLLTRRAVSREVGEKLIARIHWW 344

Query: 233 ARYYSILG---HGSFAVGNADGGLTTQEEKSLGAYAKSGASPIVGIIKPGDIPPTGGLYL 289
            +Y   +G   + + + GN  GGLTT  EKSLGA AK+G+S ++ + +        GL  
Sbjct: 345 EQYCERMGAELNNNPSAGNKAGGLTTILEKSLGAVAKAGSSNLMDVYEYAQAVTANGLVF 404

Query: 290 LDVVPDGEPRFGFPNISDNAEIGELIACGAHVILFTTGRGSVVGSAISPVIKVCANPATY 349
           +D         G+  +S   +    +A GA++I FTTGRGS  G A +P IK+  N A +
Sbjct: 405 MDTP-------GYDPVSATGQ----VAGGANLIAFTTGRGSAYGCAPAPSIKLATNSALW 453

Query: 350 RNLSGDMDVDAGRILEGRGTLDEVGREVFEQTVAVSRGAASKSET--LGHQEFI 401
                DMD++ G I E   T++  G  +FE  + ++ G  S SE    G  EF+
Sbjct: 454 ARQREDMDINCGEIAEDTLTIEACGAAIFETMLRIASGERSMSEQHGYGQNEFV 507


Lambda     K      H
   0.318    0.137    0.408 

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: 629
Number of extensions: 40
Number of successful extensions: 5
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: 431
Length of database: 515
Length adjustment: 33
Effective length of query: 398
Effective length of database: 482
Effective search space:   191836
Effective search space used:   191836
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: 51 (24.3 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