GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prdF in Pseudomonas fluorescens FW300-N2E3

Align proline racemase (EC 5.1.1.4) (characterized)
to candidate AO353_14925 AO353_14925 hydroxyproline-2-epimerase

Query= BRENDA::A8DEZ8
         (335 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_14925
          Length = 311

 Score =  199 bits (505), Expect = 1e-55
 Identities = 119/327 (36%), Positives = 183/327 (55%), Gaps = 20/327 (6%)

Query: 5   RSIQAIDSHTAGEATRIVVGGIPNIKGNSMPEKKEYLEENLDYLRTAIMLEPRGHNDMFG 64
           + I  +DSHT GE TR+V+ G P +   SM E+K  L E  D+ RTA +LEPRG + + G
Sbjct: 2   KRIHVLDSHTGGEPTRLVIAGFPELGSGSMAERKRRLAEEHDHWRTATVLEPRGSDVLVG 61

Query: 65  SVMTQPCCPDADFGIIFMDGGGYLNMCGHGTIGAMTAAIETGVVPAVEPVTHVVMEAPAG 124
           +++ +P  P+A  G+IF +  GYL MCGHGTIG + +      +  +EP  H + E P G
Sbjct: 62  ALLCEPQDPEACAGVIFFNNSGYLGMCGHGTIGLVAS---LAYLERIEPGVHRI-ETPVG 117

Query: 125 IIRGDVTVVDGKAKEVSFLNVPAFLYKEGVEVDLPGVGTVKFDISFGGSFFAIIHASQLG 184
            +   +     + + VS  NVPA+ Y++ V + LPG GT   DI++GG++F +I  +  G
Sbjct: 118 TVEATL----HEDRSVSVRNVPAYRYRKAVPLTLPGYGTASGDIAWGGNWFFLI--ADHG 171

Query: 185 LKIEPQNAGKLTELAMKLRDIINEKIEIQHPTLAHIKTVDLVEIYDEPTHPEATYKNVVI 244
            +I   N   LT     +R    E +E Q         +D +E++ +   P A  +N V+
Sbjct: 172 QRIASDNLEALTAYTWAVR----EALENQGIRGEDGGEIDHIELFAD--DPVADSRNFVL 225

Query: 245 FGQGQVDRSPCGTGTSAKLATLHAKGELKVGEKFVYESILGTLFKGEIVEETKVADFNAV 304
                 DRSPCGTGTSAKLA L A G+L+ GE +   S++G+ F+       +  D   +
Sbjct: 226 CPGKAYDRSPCGTGTSAKLACLAADGKLQPGEVWRQASVIGSQFEASY----ERLDEQRI 281

Query: 305 VPKITGSAYITGFNHFVIDEEDPLKHG 331
           +P I G A+++G +H +++E+DP   G
Sbjct: 282 IPTIRGRAHMSGESHLLLEEDDPFVWG 308


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: 297
Number of extensions: 10
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: 335
Length of database: 311
Length adjustment: 28
Effective length of query: 307
Effective length of database: 283
Effective search space:    86881
Effective search space used:    86881
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: 48 (23.1 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