GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xyrA in Pseudomonas fluorescens GW456-L13

Align D-xylose reductase (EC 1.1.1.307) (characterized)
to candidate PfGW456L13_1417 oxidoreductase, aldo/keto reductase family

Query= BRENDA::P31867
         (318 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1417
          Length = 277

 Score =  135 bits (341), Expect = 9e-37
 Identities = 94/308 (30%), Positives = 149/308 (48%), Gaps = 49/308 (15%)

Query: 9   GYDMPAVGFGCWKVDVDTCSEQIYRAIKTGYRLFDGAEDYANEKLVGAGVKKAIDEGIVK 68
           G +MP +G G W +  + C+  + +A+  GYR  D A  Y NE  VG    +A+      
Sbjct: 9   GLNMPKLGLGTWPMLGEECTRAVEQALALGYRHIDTAAAYNNEDAVG----QALANSPTP 64

Query: 69  REDLFLTSKLWNNYHHPDNVEKALNRTLSDLQVDYVDLFLIHFPVTFKFVPLEEKYPPGF 128
           RE + +T+K+W +   PD +  +++R+L  L+ +YVDLF++H+P T              
Sbjct: 65  REQIHVTTKVWWDQLQPDAMRHSMDRSLKALRSEYVDLFMLHWPTT-------------- 110

Query: 129 YCGKGDNFDYEDVPILETWKALEKLVKAGKIRSIGVSNFPGALLLDLLRGATIKPSVLQV 188
                      D  +  T + L    + G  R+IGV+NFP  LL  ++       S +QV
Sbjct: 111 -----------DWDLPRTIETLVSFREQGLARNIGVANFPLHLLRKVVEELGAPLSAIQV 159

Query: 189 EHHPYLQQPRLIEFAQSRGIAVTAYSSFGPQSFVELNQGRALNTSPLFENETIKAIAAKH 248
           E+H  L Q  L+++A+ + +A+TAY+               L  + + +   I+ IAAKH
Sbjct: 160 EYHVLLGQNALLDYARQQDLALTAYT--------------PLARNKVSDIPAIRRIAAKH 205

Query: 249 GKSPAQVLLRW-SSQRGIAIIPKSNTVPRLLENKDVNSFDLDEQDFADIAKL-----DIN 302
           G  P QV L+W   Q  +A IPK+++ P  L N       LD++D A IA L      ++
Sbjct: 206 GVLPTQVALKWLLDQPNVAAIPKASSEPNQLANLAALDVRLDDEDRALIASLSKRERQVS 265

Query: 303 LRFNDPWD 310
             F   WD
Sbjct: 266 PDFAPVWD 273


Lambda     K      H
   0.320    0.139    0.423 

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: 221
Number of extensions: 10
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: 318
Length of database: 277
Length adjustment: 26
Effective length of query: 292
Effective length of database: 251
Effective search space:    73292
Effective search space used:    73292
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 (21.8 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