GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Salinicoccus carnicancri Crm

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_017547697.1 C792_RS0101610 threonine/serine dehydratase

Query= SwissProt::Q9WYJ1
         (401 letters)



>NCBI__GCF_000330705.1:WP_017547697.1
          Length = 319

 Score =  221 bits (563), Expect = 2e-62
 Identities = 125/314 (39%), Positives = 185/314 (58%), Gaps = 4/314 (1%)

Query: 2   ITLEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAH 61
           +TL  I+EA   +   +  T L   + L    G E+YLKME++QKT +FKIRGA NKI  
Sbjct: 3   LTLNRIEEASERIAPYIQETPLLRMNNLDPFLGCEVYLKMESMQKTNAFKIRGAMNKILQ 62

Query: 62  LSEEERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVILEG 121
           L E + +RG++  S+GNH + VA AA+  GI AT+V+P    + K      LGA +I   
Sbjct: 63  LPESDLERGIITTSSGNHGRAVAFAAKQLGIHATVVVPESGSIFKADAIEALGADLIRCD 122

Query: 122 NIFDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVGGGGL 181
               E +E    + EK    ++ PF+D  V+AGQGT+GLEI      ++ V++P  GGGL
Sbjct: 123 --VRERFEVTEALAEKYDYTYIPPFDDYGVMAGQGTVGLEITSQNKLLDHVIMPASGGGL 180

Query: 182 ISGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLADGIAVKKPGDLTF 241
           +S  S AIK   P++KV G +  N+P    SL +G    V  K T+AD +   +PG   F
Sbjct: 181 LSSSSTAIKLTAPDMKVYGAEPANLPRYTKSLAKGEVTAVTRKETVADALVTSQPGTRNF 240

Query: 242 ELVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVL-NKLDVKGK-KVAIV 299
            +V++YVD M+ V+EE I   I  L+ +AK+VAE + A+   A+L   LDV  + KV +V
Sbjct: 241 PIVQEYVDGMMTVSEEFILKGIKLLMMEAKIVAEPSSAITAGALLEGSLDVSPEDKVCLV 300

Query: 300 ISGGNIDVNMIDRI 313
           ISGGN+ ++ ++++
Sbjct: 301 ISGGNVGLDFLEKL 314


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: 247
Number of extensions: 12
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: 401
Length of database: 319
Length adjustment: 29
Effective length of query: 372
Effective length of database: 290
Effective search space:   107880
Effective search space used:   107880
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 Jul 26 2024. The underlying query database was built on Jul 25 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