GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt2d in Pseudomonas fluorescens FW300-N2C3

Align mannitol 2-dehydrogenase (EC 1.1.1.67) (characterized)
to candidate AO356_28545 AO356_28545 alcohol dehydrogenase

Query= BRENDA::Q8KQG6
         (338 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_28545
          Length = 343

 Score =  176 bits (445), Expect = 1e-48
 Identities = 104/335 (31%), Positives = 176/335 (52%), Gaps = 16/335 (4%)

Query: 1   MEALVLTGTKKLEVKDIDRPKVLPNEVLIHTAFAGICGTDHALYAGLPGSADAVPPIVLG 60
           M+A  +    +  +  +D+P+V   EV +  A+AGICG+D  +  G   +A    P V G
Sbjct: 1   MKAFQVRAPFEFGLAQVDQPQVAHGEVQVDVAYAGICGSDMHIIHGQ--NAFVRFPRVTG 58

Query: 61  HENSGVVAEIGSAVTNVKVGDRVTVDPNIYCGQCKYCRTARPELCENLSAVGVTRDGGFE 120
           HE SGV+ ++G  V +++VGDRV +DP I CG C  CR  RP +C  L  +GV RDGGF 
Sbjct: 59  HEFSGVIRQVGEGVEHLQVGDRVCIDPVISCGTCYPCRIGRPNVCTRLQVIGVHRDGGFS 118

Query: 121 EFFTAPASVVYPIPDNVSLKSAAVVEPISCAVHGIQLLKVTPYQKALVIGDGFMGELFVQ 180
           E    PA   + +PD +SL   A+VEP S A++ +  ++  P    L+ G G +G   VQ
Sbjct: 119 EQVCVPAENAHRLPDAMSLSHGALVEPYSIALNVLDRMQPHPGDSVLIYGAGVIGLTLVQ 178

Query: 181 ILQAYGIHQVDLAGIVDEKLAMNKEKFGVKNTYNTMKGD------KIPEGE-YDVIIEAV 233
           + +A G+  + +  ++D +L       G   T N  + D      ++ +GE   +I++A 
Sbjct: 179 MARALGLTDITVTDVIDSRLE-TARALGASRTLNGQQVDVEAVMRELTQGEGVPLIVDAA 237

Query: 234 GLPQTQEAAIEASARGAQVLMFGVGGPDAKFQMNTYEVFQKQLTIQGSFINPNAFEDSLA 293
            +P      +  ++   ++ + G     +   +   E+ +K+LT+ GS +N   F   + 
Sbjct: 238 CIPALMPQMVRLASPAGRIGLLGFNATPS--DLVQLEMIKKELTLVGSRLNNRKFPRVIE 295

Query: 294 LLSSGKLNVEALMSHELDYKTVDDFVNGKLGVVSK 328
           L++SGKL V+ L+SH + +    D + G + ++ K
Sbjct: 296 LIASGKLQVQDLISHRVSF----DEMPGAIDLIEK 326


Lambda     K      H
   0.317    0.136    0.390 

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: 266
Number of extensions: 15
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: 338
Length of database: 343
Length adjustment: 28
Effective length of query: 310
Effective length of database: 315
Effective search space:    97650
Effective search space used:    97650
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: 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