GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xyrA in Pseudomonas fluorescens FW300-N1B4

Align NAD(P)H-dependent D-xylose reductase XYR1; XR; EC 1.1.1.307 (characterized)
to candidate Pf1N1B4_128 Methylglyoxal reductase, acetol producing (EC 1.1.1.-) / 2,5-diketo-D-gluconic acid reductase B (EC 1.1.1.274)

Query= SwissProt::G4N708
         (324 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_128
          Length = 267

 Score =  141 bits (355), Expect = 2e-38
 Identities = 93/301 (30%), Positives = 147/301 (48%), Gaps = 43/301 (14%)

Query: 12  LDMPQVGFGLWKVENSVCADVVYNAIKAGYRLFDGACDYGNEVECGQGVKRAIDEGLVKR 71
           + +P  G G ++++  V  D V   ++ GYR+ D A  Y NE E GQ    AI    + R
Sbjct: 1   MSIPAFGLGTFRLQGQVVIDSVSTGLELGYRVIDTAQIYKNEAEVGQ----AIAASGIAR 56

Query: 72  EELFIVSKLWNTFHDGERVEPIVKKQLADWGIEYFDLYLIHFPVALEYVDPSVRYPPGWH 131
           +ELFI SK+W      +R+   +K+ L     +Y DL LIH+P       P  + P    
Sbjct: 57  DELFITSKIWVANFAKDRLIDSLKESLNKLQTDYLDLTLIHWP------SPEDQVP---- 106

Query: 132 YDDAGTEIRPSKASIQETWTAMEKLVDAGLSKAIGVSNFQAQLLYDMLRYARIRP-ATLQ 190
                         ++E   A+ +    GL++ IGVSNF   L+   +        AT Q
Sbjct: 107 --------------VEEFMGALLQAKQLGLTRKIGVSNFTVDLMQQAITAIGAENIATNQ 152

Query: 191 IEHHPYLVQQRLIEACKTEGIVVTAYSSFGPASFKEFNMEHAEALTPLLEEPTIVKLAEK 250
           IE HPYL  ++++E  +++GI +T+Y +               A   +L++P I ++A++
Sbjct: 153 IELHPYLQNRKVVEFAQSQGIRITSYMTL--------------AYGEVLKDPLIQQIADR 198

Query: 251 YGKDPGQVLLRWATQRGLAVIPKSSREKTMKSNFEAVGWDMEDSDIKTISALDKGIRFNQ 310
               P QV L WA Q G AVIP S++   ++ N +A    + D+D+  I+ALD+G R   
Sbjct: 199 LQATPAQVTLAWAMQLGYAVIPSSTKRANLQGNLQACALTLSDADMALIAALDRGQRLTS 258

Query: 311 P 311
           P
Sbjct: 259 P 259


Lambda     K      H
   0.319    0.136    0.418 

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: 172
Number of extensions: 6
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: 324
Length of database: 267
Length adjustment: 26
Effective length of query: 298
Effective length of database: 241
Effective search space:    71818
Effective search space used:    71818
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