GapMind for catabolism of small carbon sources

 

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

Align proline racemase (EC 5.1.1.4) (characterized)
to candidate Pf6N2E2_671 2-methylaconitate racemase

Query= BRENDA::A8DEZ8
         (335 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_671
          Length = 342

 Score =  190 bits (482), Expect = 5e-53
 Identities = 110/337 (32%), Positives = 178/337 (52%), Gaps = 5/337 (1%)

Query: 1   MKFSRSIQAIDSHTAGEATRIVVGGIPNIKGNSMPEKKEYLEENLDYLRTAIMLEPRGHN 60
           M+ S+ I  +  H  GE   ++VGG+    G ++ E+  ++ ++   LR  ++ EPRG  
Sbjct: 1   MRSSKIIHVVSCHAEGEVGDVIVGGVAPPPGATVWEQSRWIAQD-QTLRNFVLNEPRGGV 59

Query: 61  DMFGSVMTQPCCPDADFGIIFMDGGGYLNMCGHGTIGAMTAAIETGVVPAVEPVTHVVME 120
               +++     P A    I M+      M G  ++   T  +++G++P  EP T +V+E
Sbjct: 60  FRHVNLLVPAKDPRAQMAWIIMEPADTPPMSGSNSLCVATVLLDSGILPMTEPQTRLVLE 119

Query: 121 APAGIIRGDVTVVDGKAKEVSFLNVPAFLYKEGVEVDLPGVGTVKFDISFGGSFFAIIHA 180
           AP G+I       DGK + V   NVP+F  +    +++ G+G+++ D ++GG  F I+ A
Sbjct: 120 APGGLIEAVADCRDGKVQRVEIKNVPSFADRLDAWIEVEGLGSLQVDTAYGGDSFVIVDA 179

Query: 181 SQLGLKIEPQNAGKLTELAMKLRDIINEKIEIQHPTLAHIKTVDLVEIYDEPTHPE---A 237
            +LG  I P  A +L  + +K+    NE++   HP       +   +I   P   E   A
Sbjct: 180 QRLGFAIRPDEAAELVAVGLKITRAANEQLGFVHPLNPDWSHISFCQI-AAPIVQENGIA 238

Query: 238 TYKNVVIFGQGQVDRSPCGTGTSAKLATLHAKGELKVGEKFVYESILGTLFKGEIVEETK 297
           T  N V+   G++DRSP GTG SA++A LHAKG ++VGE+F+  SI+G+ F   I   T 
Sbjct: 239 TGANAVVIQPGKIDRSPTGTGCSARMAVLHAKGLMQVGERFIGRSIIGSEFHCRIDSLTD 298

Query: 298 VADFNAVVPKITGSAYITGFNHFVIDEEDPLKHGFIL 334
           VA   A+ P I G A+ITG +  ++D  DP   G+ L
Sbjct: 299 VAGRPAIYPCIAGRAWITGTHQLLLDPADPWPQGYRL 335


Lambda     K      H
   0.319    0.139    0.403 

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: 266
Number of extensions: 10
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: 335
Length of database: 342
Length adjustment: 28
Effective length of query: 307
Effective length of database: 314
Effective search space:    96398
Effective search space used:    96398
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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