GapMind for catabolism of small carbon sources

 

Aligments for a candidate for mmsB in Burkholderia phytofirmans PsJN

Align 3-hydroxyisobutyrate dehydrogenase (EC 1.1.1.31) (characterized)
to candidate BPHYT_RS24130 BPHYT_RS24130 tartronate semialdehyde reductase

Query= reanno::psRCH2:GFF2390
         (296 letters)



>lcl|FitnessBrowser__BFirm:BPHYT_RS24130 BPHYT_RS24130 tartronate
           semialdehyde reductase
          Length = 297

 Score =  164 bits (415), Expect = 2e-45
 Identities = 112/286 (39%), Positives = 148/286 (51%), Gaps = 9/286 (3%)

Query: 4   GFIGLGNMGAPMAHNLLKAGHQLSVFDLNAAAVENLVGAGALPVDSPTAIAQGNAELIIT 63
           GFIGLG MG PMA NLLK G  L+ F   +   ++LV AGA+  DSP A+    A++I  
Sbjct: 5   GFIGLGIMGKPMAANLLKNGVALAAFT-RSGVPDDLVQAGAVACDSPAAVG-AQADVIFI 62

Query: 64  MLPAAAHVKGVYLGVNGLIAHSRAGVMLIDCSTIDPHSAREVAKAAAEHGNPMLDAPVSG 123
           M+P    V+ V  G  GL +  RAG  ++D S+I P + RE A    E G   LDAPVSG
Sbjct: 63  MVPDTPDVERVLFGEQGLASVLRAGQTVVDMSSISPMATREFAARVRESGADYLDAPVSG 122

Query: 124 GTGGAAAGTLTFMVGGSDPDFDHAQPILAAMGKNIVHCGAAGNGQVAKVANNMLLGISMI 183
           G  GA AG+LT MVGG    FD  +P+   MGKN+   G  G GQV KVAN +++  ++ 
Sbjct: 123 GEVGAKAGSLTIMVGGETATFDAVKPLFDMMGKNVTLIGGVGAGQVCKVANQVIVAATIE 182

Query: 184 GVAEAMALGVALGMDAKTLAGVINTSSGRCWSSDTYNPFPGVLDNVPSSRGYSGGFGSDL 243
            V EA+ L    G+D    A V     G   SS        V     + R +  GF  +L
Sbjct: 183 AVGEALLLASKAGVDP---ARVREALMGGFASSRILE----VHGERMTKRTFDPGFRIEL 235

Query: 244 MLKDLGLATEAAKQVRQPVILGALAQQLYQSFSAQGHGGLDFSAII 289
             KDL LA   A+ +   +   A  Q L+ +  A G    D SA++
Sbjct: 236 HQKDLNLALSTAQSLGVSLPNTATCQALFNACVAHGGKAWDHSAMV 281


Lambda     K      H
   0.318    0.134    0.392 

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: 249
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: 296
Length of database: 297
Length adjustment: 26
Effective length of query: 270
Effective length of database: 271
Effective search space:    73170
Effective search space used:    73170
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 (21.7 bits)
S2: 48 (23.1 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 preprint 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