GapMind for catabolism of small carbon sources

 

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

Align NAD-dependent glycerol dehydrogenase; Dha-forming NAD-dependent glycerol dehydrogenase; EC 1.1.1.6 (characterized)
to candidate AO353_01660 AO353_01660 short-chain dehydrogenase

Query= SwissProt::Q92EU6
         (254 letters)



>lcl|FitnessBrowser__pseudo3_N2E3:AO353_01660 AO353_01660
           short-chain dehydrogenase
          Length = 253

 Score =  139 bits (349), Expect = 7e-38
 Identities = 91/260 (35%), Positives = 150/260 (57%), Gaps = 19/260 (7%)

Query: 1   MTFKGFDKDFNITDKVAVVTGAASGIGKAMAELFSEKGAYVVLLDIKEDVKDVAAQINPS 60
           MTF G         +VA+VTGAA+GIG+A A+ F+ +G  VV+ D+     +  A++  +
Sbjct: 3   MTFSG---------QVALVTGAAAGIGRATAQAFAAEGLKVVVADLDVAGGEGTAELIRA 53

Query: 61  ---RTLALQVDITKKENIEKVVAEIKKVYPKIDILANSAGVALLEK---AEDLPEEYWDK 114
                + +Q ++T++ +++ ++A+    Y ++D   N+AG+ + EK   AE   +E+ D 
Sbjct: 54  AGGEAVFVQCNVTQESDVQNLMAKAVSTYGRLDYAFNNAGIEI-EKGKLAEGTLDEF-DA 111

Query: 115 TMELNLKGSFLMAQIIGREMIATGGGKIVNMASQASVIALDKHVAYCASKAAIVSMTQVL 174
            M +N+KG +L  +     M+A GGG IVN AS A + A  K   Y ASK A++ +T+  
Sbjct: 112 IMGVNVKGVWLCMKYQLPLMLAQGGGAIVNTASVAGLGAAPKMSIYAASKHAVIGLTKSA 171

Query: 175 AMEWAPYNINVNAISPTVILTELGKKAWAG--QVGEDMKKLIPAGRFGYPEEVAACALFL 232
           A+E+A   I VNA+ P VI T++ ++A+    +  +    + P GR G  EE+A+  L+L
Sbjct: 172 AIEYAKKKIRVNAVCPAVIDTDMFRRAYEADPKKADFAAAMHPVGRIGKVEEIASAVLYL 231

Query: 233 VSDAASLITGENLIIDGGYT 252
            SD A+  TG +L +DGG T
Sbjct: 232 CSDGAAFTTGHSLAVDGGVT 251


Lambda     K      H
   0.316    0.133    0.369 

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: 142
Number of extensions: 10
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: 254
Length of database: 253
Length adjustment: 24
Effective length of query: 230
Effective length of database: 229
Effective search space:    52670
Effective search space used:    52670
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.

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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 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