GapMind for catabolism of small carbon sources

 

Aligments for a candidate for yvgN in Pseudomonas fluorescens FW300-N2E3

Align Glyoxal reductase; GR; Methylglyoxal reductase; EC 1.1.1.-; EC 1.1.1.283 (characterized)
to candidate AO353_19655 AO353_19655 2,5-diketo-D-gluconic acid reductase

Query= SwissProt::O32210
         (276 letters)



>lcl|FitnessBrowser__pseudo3_N2E3:AO353_19655 AO353_19655
           2,5-diketo-D-gluconic acid reductase
          Length = 267

 Score =  176 bits (445), Expect = 6e-49
 Identities = 99/257 (38%), Positives = 147/257 (57%), Gaps = 5/257 (1%)

Query: 15  VEMPWFGLGVFKVENGNEATESVKAAIKNGYRSIDTAAIYKNEEGVGIGIKESGVAREEL 74
           + +P FGLG F+++ G    +SV   ++ GYR+IDTA IY NE  VG  I  SG+AREEL
Sbjct: 1   MSVPAFGLGTFRLQ-GQVVIDSVSTGLELGYRAIDTAQIYDNEADVGQAIAASGIAREEL 59

Query: 75  FITSKVWNEDQGYETTLAAFEKSLERLQLDYLDLYLIHWPGKDK---YKDTWRALEKLYK 131
           FITSK+W  +   +  +A+ + SL +LQ DYLDL LIHWP  +      +   AL +   
Sbjct: 60  FITSKIWIANFAKDQLIASLKDSLRKLQTDYLDLTLIHWPSPENQVPVHEFMGALLEAKA 119

Query: 132 DGKIRAIGVSNFQVHHLEELLKDAEIKPM-VNQVEFHPRLTQKELRDYCKGQGIQLEAWS 190
            G  R IGVSNF V  +++ +       +  NQ+E HP L  + + ++ + QGIQ+ ++ 
Sbjct: 120 LGLTRQIGVSNFTVDLMQQAIDAVGADNIATNQIELHPYLQNRTVVEFAQSQGIQITSYM 179

Query: 191 PLMQGQLLDNEVLTQIAEKHNKSVAQVILRWDLQHGVVTIPKSIKEHRIIENADIFDFEL 250
            L  G++L + V+ QIAE+H  + AQV L W +Q G   IP S +   +  N    +  L
Sbjct: 180 TLAYGEVLKDPVIQQIAERHQATPAQVTLAWAMQQGYAVIPSSTQRANLDSNLAARELTL 239

Query: 251 SQEDMDKIDALNKDERV 267
           S+ DM  I  L + +R+
Sbjct: 240 SEADMTLIAGLERGQRL 256


Lambda     K      H
   0.316    0.135    0.397 

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: 194
Number of extensions: 9
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: 276
Length of database: 267
Length adjustment: 25
Effective length of query: 251
Effective length of database: 242
Effective search space:    60742
Effective search space used:    60742
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 47 (22.7 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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