GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prdF in Pseudomonas fluorescens FW300-N2C3

Align proline racemase (EC 5.1.1.4) (characterized)
to candidate AO356_09240 AO356_09240 hydroxyproline-2-epimerase

Query= BRENDA::A8DEZ8
         (335 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_09240
          Length = 332

 Score =  237 bits (604), Expect = 4e-67
 Identities = 127/330 (38%), Positives = 189/330 (57%), Gaps = 1/330 (0%)

Query: 5   RSIQAIDSHTAGEATRIVVGGIPNIKGNSMPEKKEYLEENLDYLRTAIMLEPRGHNDMFG 64
           RS   IDSH  G   R+V GG P +   SM E++E    + D++RTA+M EPRGH+ M G
Sbjct: 3   RSFFCIDSHACGNPVRVVAGGGPLLPSVSMAERREIFVRDHDWVRTALMFEPRGHDIMSG 62

Query: 65  SVMTQPCCPDADFGIIFMDGGGYLNMCGHGTIGAMTAAIETGVVPAVEPVTHVVMEAPAG 124
            ++      D DFG +F++  G L MCG GTIG  T  IE G+V   EP   + +E PAG
Sbjct: 63  VIIYPSTREDCDFGALFIEVSGCLPMCGAGTIGLSTVVIEEGLVTPKEP-GKLAIETPAG 121

Query: 125 IIRGDVTVVDGKAKEVSFLNVPAFLYKEGVEVDLPGVGTVKFDISFGGSFFAIIHASQLG 184
            +  + T+     + +   NV ++L+   V V +PGVG +  DI++GG+F+A++   Q  
Sbjct: 122 RVDVEYTLDGEYVESIKLFNVASYLHSADVVVQVPGVGQLTVDIAYGGNFYAVVEPQQCW 181

Query: 185 LKIEPQNAGKLTELAMKLRDIINEKIEIQHPTLAHIKTVDLVEIYDEPTHPEATYKNVVI 244
             ++  +   +  L++KLR  +       HP    I  V  V   D+P +  A  +  V 
Sbjct: 182 PGLDGHSTADIVGLSVKLRAALAGICNPLHPENERITGVHHVIWCDKPQNSTADGRCAVF 241

Query: 245 FGQGQVDRSPCGTGTSAKLATLHAKGELKVGEKFVYESILGTLFKGEIVEETKVADFNAV 304
           +G   +DRSP GTGTSA++A L  KG LKVG+ + +ES +GTL++G++    KV +F+ +
Sbjct: 242 YGDKAIDRSPGGTGTSARMAQLFGKGRLKVGDTYRHESPIGTLYEGKVEAAIKVGEFDGI 301

Query: 305 VPKITGSAYITGFNHFVIDEEDPLKHGFIL 334
            P ITG A +TG+N   +D+ DPL HGF L
Sbjct: 302 RPSITGWAQVTGYNTLFVDDRDPLAHGFQL 331


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: 327
Number of extensions: 14
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: 335
Length of database: 332
Length adjustment: 28
Effective length of query: 307
Effective length of database: 304
Effective search space:    93328
Effective search space used:    93328
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.

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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