GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Pseudomonas fluorescens FW300-N2E2

Align L-threonine ammonia-lyase; L-serine ammonia-lyase; Threonine dehydratase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate Pf6N2E2_1562 Threonine dehydratase (EC 4.3.1.19)

Query= SwissProt::Q9WYJ1
         (401 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1562
          Length = 318

 Score =  183 bits (464), Expect = 7e-51
 Identities = 110/307 (35%), Positives = 172/307 (56%), Gaps = 3/307 (0%)

Query: 2   ITLEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAH 61
           +T +DI++A R L  V+  TA     +L+E  G  +++K EN   TG+FK+RG    +  
Sbjct: 4   LTRDDIEQAARHLYEVMPATAQYAWPLLAERLGCTVWVKHENHTPTGAFKVRGGLTFVRW 63

Query: 62  LSEEERK-RGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVILE 120
           L  E  + +G+V A+ GNH Q +ALAA   G+ A IV+P+   + K    R  G +V+  
Sbjct: 64  LKREHPEAKGIVTATRGNHGQSLALAASALGLKALIVVPQGNSVEKNNAMRGFGGEVVEY 123

Query: 121 GNIFDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVGGGG 180
           G  FDEA E A+R+ +  G   V PF+ P ++ G  T GLE+   +PD++ V VP+G G 
Sbjct: 124 GRDFDEAREEAVRLAQSHGLYLVPPFH-PELVKGVATYGLELFNAVPDLDTVYVPIGCGS 182

Query: 181 LISGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLADGIAVKKPGDLT 240
            I  V  A  ++  + +V+GV +    +   S   GR        T ADG+AV++P    
Sbjct: 183 GICAVIAARDALGLKTQVVGVVSTEALAAKLSFEAGRLCETASANTFADGLAVRRPVPEA 242

Query: 241 FELVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVLNKLD-VKGKKVAIV 299
           F +       +VAV++ EIA A+         +AEGAGA  +AA++ + + ++GK+VA++
Sbjct: 243 FAIYGAGAARIVAVSDAEIAGAMRAYYTDTHNLAEGAGAAALAALMQERETMRGKRVAVI 302

Query: 300 ISGGNID 306
           +SGGNID
Sbjct: 303 LSGGNID 309


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: 245
Number of extensions: 15
Number of successful extensions: 4
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: 318
Length adjustment: 29
Effective length of query: 372
Effective length of database: 289
Effective search space:   107508
Effective search space used:   107508
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