GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Echinicola vietnamensis KMM 6221, DSM 17526

Align L-threonine ammonia-lyase; L-serine ammonia-lyase; Threonine dehydratase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate Echvi_1189 Echvi_1189 Threonine dehydratase

Query= SwissProt::Q9WYJ1
         (401 letters)



>FitnessBrowser__Cola:Echvi_1189
          Length = 319

 Score =  178 bits (452), Expect = 2e-49
 Identities = 108/310 (34%), Positives = 176/310 (56%), Gaps = 6/310 (1%)

Query: 4   LEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAHLS 63
           L DIK+A + +   +H T +     ++++   ++Y K EN QK G+FK RGA N I  L 
Sbjct: 10  LIDIKQAYQRIMAYIHHTPILTCEAINKMADCQLYFKCENFQKVGAFKARGATNAILKLP 69

Query: 64  EEERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVI-LEGN 122
              +K GV   S+GNHA  +A AA+  G  A IVMP  A   K    R  G ++I  E N
Sbjct: 70  PGLKKNGVATHSSGNHAAALARAAKETGTKAYIVMPSTAAAIKKAAVRTYGGEIIECEPN 129

Query: 123 IFDEAYEAAL-RIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVGGGGL 181
           +  +A E  L ++ E+TGA F+ P++   VI GQ T  LE+ ++    + ++ PVGGGGL
Sbjct: 130 L--KARETTLEKVVEETGAAFIPPYDYMDVIEGQATCALEMWDEGIPFDAIITPVGGGGL 187

Query: 182 ISGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLADGIAVKKPGDLTF 241
           ++G ++    ++ +  V G + +       SL+  +   +E   T+ADG+ +   G   F
Sbjct: 188 LAGTALTTHYLSRKTPVYGAEPKGADDAYRSLKANKIIPMENPNTIADGL-LTSLGKRNF 246

Query: 242 ELVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVL-NKLDVKGKKVAIVI 300
            ++ K V +++ V++++I  A+  + E+ K+V E + AV +AA+L NK   + K+V IVI
Sbjct: 247 TIISKNVADILTVSDDQIIAAMRLVFERMKLVIEPSSAVPLAAILANKPLFQNKRVGIVI 306

Query: 301 SGGNIDVNMI 310
           SGGN+DV+ +
Sbjct: 307 SGGNVDVSKL 316


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: 218
Number of extensions: 8
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 Apr 09 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