GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Pseudomonas fluorescens FW300-N2E2

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate Pf6N2E2_4819 Alcohol dehydrogenase (EC 1.1.1.1)

Query= ecocyc::EG12293-MONOMER
         (383 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_4819
          Length = 382

 Score =  243 bits (619), Expect = 9e-69
 Identities = 145/383 (37%), Positives = 217/383 (56%), Gaps = 3/383 (0%)

Query: 1   MAASTFFIPSVNVIGADSLTDAMNMMADYGFTRTLIVTDNMLTKLGMAGDVQKALEERNI 60
           M+ S+F I    + GA ++      +        LIVTD  L K G      + L  R+ 
Sbjct: 1   MSLSSFKIAHKLITGAAAIEQLAAELTRLDVDNPLIVTDAALVKSGTVELALQHLGGRDY 60

Query: 61  FSVIYDGTQPNPTTENVAAGLKLLKENNCDSVISLGGGSPHDCAKGIALVAANGGDIRDY 120
              I+D   P+P    V   ++  ++   D +I LGGGS  D AK + + A   G+++D 
Sbjct: 61  --EIFDRVMPDPEIAIVEDCMQAYRDGGHDGLIGLGGGSAIDIAKCVGVYAGYHGELQDM 118

Query: 121 EGVDRSAKPQLPMIAINTTAGTASEMTRFCIITDEARHIKMAIVDKHVTPLLSVNDSSLM 180
            GVD+  +   PMIAI TTAGT SE+T   I++D+A  +K  IV  ++ P +++    + 
Sbjct: 119 FGVDQVPRKGPPMIAIPTTAGTGSEVTNVAILSDKAAQLKKGIVSDYLLPDVALVSPQMT 178

Query: 181 IGMPKSLTAATGMDALTHAIEAYVSIAATPITDACALKAVTMIAENLPLAVEDGSNAKAR 240
           +  P+ +TAA+G+DAL HAIEAY+S+ A+PITDA A+ A+ +I+  LP A  + ++ +AR
Sbjct: 179 LTCPRGVTAASGVDALAHAIEAYLSLNASPITDALAIGAIKLISRALPKAYANPAHLQAR 238

Query: 241 EAMAYAQFLAGMAFNNASLGYVHAMAHQLGGFYNLPHGVCNAVLLPHVQVFNSKVAAARL 300
           E MA A  +AGMAF NA +G VHA+A+ LGG +++ HGV NA+LLP+V  +N      R+
Sbjct: 239 EDMATASLMAGMAFGNAGVGAVHALAYPLGGRFHVSHGVANAMLLPYVMTWNKMACVERM 298

Query: 301 RDCAAAMGVNVTGKNDAEGAEACINAIRELAKKVDIPAGLRDLNVKEEDFAVLATNALK- 359
           RD A AMG+     +D E A+  + A+  L   V+IP GL  L V E+    +A  A   
Sbjct: 299 RDIAEAMGLKTAHLSDLEAADEAVEAMITLCAAVEIPQGLSSLGVTEDVIPSMAVEAAGI 358

Query: 360 DACGFTNPIQATHEEIVAIYRAA 382
           +     NP + +  +I  IYRAA
Sbjct: 359 ERLMRNNPRKLSAADIEKIYRAA 381


Lambda     K      H
   0.318    0.131    0.373 

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: 358
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: 383
Length of database: 382
Length adjustment: 30
Effective length of query: 353
Effective length of database: 352
Effective search space:   124256
Effective search space used:   124256
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 (21.8 bits)
S2: 50 (23.9 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