GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gyaR in Echinicola vietnamensis KMM 6221, DSM 17526

Align Glyoxylate reductase; EC 1.1.1.26 (uncharacterized)
to candidate Echvi_3161 Echvi_3161 Lactate dehydrogenase and related dehydrogenases

Query= curated2:Q9YAW4
         (335 letters)



>FitnessBrowser__Cola:Echvi_3161
          Length = 331

 Score =  139 bits (350), Expect = 1e-37
 Identities = 95/300 (31%), Positives = 151/300 (50%), Gaps = 24/300 (8%)

Query: 40  LLSKAREADALYTLLTDRIDCDLLSQAPRLRI--VAQMAVGFDNIDVECATRLGIYVTNT 97
           LL++  +A AL++   D    ++L    +L I  +A  + GF+++D+E A  L I V   
Sbjct: 39  LLAEGSKAIALFS--NDDASSEVLDILHKLGIKFIALRSAGFNHVDLEKAAELNIKVARV 96

Query: 98  PGVLTEATAEFTWALILAAARRVVEADHFVRWGEWWRLRTGWHPMMMLGVELRGKTLGIL 157
           P     A AE T ALILA  RR+++A + VR          +    + G +L GKT+G++
Sbjct: 97  PAYSPYAIAEHTMALILALNRRLIKAHNRVR-------EQNFSLNGLTGFDLNGKTVGVI 149

Query: 158 GMGRIGSRVAEIGKAFGMRIIYHSRSRKREIEKELGAEYRSLEDLLRESDILSIHLPLTD 217
           G G+IGS + +I   FG  I+       +++  + G  Y     L + +DI+S+H+PL  
Sbjct: 150 GTGKIGSVLVKILHGFGCNILAQDIEESKDLIDKYGLIYSDCATLCKHADIISLHVPLKA 209

Query: 218 ETRHLIGESELKLMKKTAILVNTGRGAIVDTGALVKALREGWIAAAALDVFEEEP--LNP 275
            T+HLI +  + LMK   +L+NT RG +VDT A+++ L+   I    LDV+EEE      
Sbjct: 210 STKHLINKEHIALMKSGVMLINTSRGGLVDTKAVIEGLKTKKIGYLGLDVYEEEEGLFFE 269

Query: 276 NHP-----------LTAFKNVVLAPHAASATRETRLRMAMMAAENLVAFAQGKVPPNLVN 324
           +H            L  F NV++  H A  T+     +A     NL  F + K   N ++
Sbjct: 270 DHSDDILQDDVIARLMTFNNVLITSHQAFLTKTALTNIAETTIYNLDCFEKQKPSGNEIS 329


Lambda     K      H
   0.322    0.136    0.406 

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: 223
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: 335
Length of database: 331
Length adjustment: 28
Effective length of query: 307
Effective length of database: 303
Effective search space:    93021
Effective search space used:    93021
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 (21.9 bits)
S2: 49 (23.5 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