GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Burkholderia vietnamiensis G4

Align L-threonine ammonia-lyase; L-serine ammonia-lyase; Threonine dehydratase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate WP_011882283.1 serine/threonine dehydratase

Query= SwissProt::Q9WYJ1
         (401 letters)



>NCBI__GCF_000016205.1:WP_011882283.1
          Length = 325

 Score =  229 bits (583), Expect = 1e-64
 Identities = 112/306 (36%), Positives = 187/306 (61%), Gaps = 1/306 (0%)

Query: 3   TLEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAHL 62
           T +D+  A   L+   HRT +  SS L +  G +++ K ENLQ+ G+FK RGA+N ++  
Sbjct: 8   TYDDVAAAAARLQGHAHRTPVMTSSTLDDALGAQVFFKCENLQRMGAFKFRGAFNALSRF 67

Query: 63  SEEERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVILEGN 122
              +R+ GVV  S+GNHAQ +AL+A++ GIPATIVMP+ AP +K+  TR  G  V+    
Sbjct: 68  DATQRRNGVVTFSSGNHAQAIALSARMLGIPATIVMPQDAPAAKMAATRGYGGNVVTYDR 127

Query: 123 IFDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVGGGGLI 182
             ++  +    + EK G   + P++   VIAGQGT   E+ +++  ++ V  P+GGGGL+
Sbjct: 128 YTEDREQIGRELAEKHGLTLIPPYDHADVIAGQGTAAKELFDEVGPLDAVFAPLGGGGLL 187

Query: 183 SGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLADGIAVKKPGDLTFE 242
           SG ++A ++++P+ K+ GV+ E       S R G    ++   T+ADG   +  G+LTF+
Sbjct: 188 SGTALATRALSPQAKLYGVEPEAGNDGQQSFRSGAIVHIDTPRTIADGAQTQHLGNLTFQ 247

Query: 243 LVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVLN-KLDVKGKKVAIVIS 301
           ++++ VD+++   + E+ D++ F   + K++ E  G + +AA    K ++ GK+V IVIS
Sbjct: 248 ILRRDVDDILTATDAELVDSMRFFATRMKLIVEPTGCLSLAAARKMKDELAGKRVGIVIS 307

Query: 302 GGNIDV 307
           GGN+D+
Sbjct: 308 GGNVDL 313


Lambda     K      H
   0.317    0.136    0.367 

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: 237
Number of extensions: 9
Number of successful extensions: 2
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: 401
Length of database: 325
Length adjustment: 29
Effective length of query: 372
Effective length of database: 296
Effective search space:   110112
Effective search space used:   110112
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 Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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