GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Pseudomonas simiae WCS417

Align L-threonine ammonia-lyase; L-serine ammonia-lyase; Threonine dehydratase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate GFF2535 PS417_12925 serine dehydratase

Query= SwissProt::Q9WYJ1
         (401 letters)



>FitnessBrowser__WCS417:GFF2535
          Length = 321

 Score =  240 bits (613), Expect = 4e-68
 Identities = 113/315 (35%), Positives = 201/315 (63%), Gaps = 1/315 (0%)

Query: 3   TLEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAHL 62
           T +D+ +A + L+ V H T +  S  L  +TG ++++K E+LQ+ GSFK RGA+N ++  
Sbjct: 5   TYQDVIDAAQRLEGVAHATPVFTSRTLDALTGAQVFIKCEHLQRAGSFKFRGAFNALSQF 64

Query: 63  SEEERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVILEGN 122
           + ++RK GVVA S+GNHAQG+ALAAQ+ GIPATIVMP  AP +K+  TR  GA V+L   
Sbjct: 65  NPQQRKAGVVAFSSGNHAQGIALAAQLLGIPATIVMPTDAPAAKVAATREYGASVVLYDR 124

Query: 123 IFDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVGGGGLI 182
             ++  +    +  + G   + P++ PH++AGQGT   E++E    ++ + V +GGGG++
Sbjct: 125 FTEDREQIGRNLATEQGLTLIPPYDHPHILAGQGTAAKELLESTGPLDALFVGLGGGGML 184

Query: 183 SGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLADGIAVKKPGDLTFE 242
           SG +++ ++++P+  + GV+ E       S R G    ++   T+ADG   +  G+ TF 
Sbjct: 185 SGTALSTRALSPDCLLYGVEPEAGNDGQRSFRSGSIVHIDTPKTIADGAQTQHLGNYTFP 244

Query: 243 LVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVLNKLD-VKGKKVAIVIS 301
           +++  V++++ V++ E+  A+ F +++ K+V E  G +G+AA+LN+    KG++V I+++
Sbjct: 245 IIRDNVNDILTVSDAELVAAMKFFMQRMKMVVEPTGCLGLAALLNEAGRFKGQRVGIIVT 304

Query: 302 GGNIDVNMIDRIINK 316
           GGN+D+     ++++
Sbjct: 305 GGNVDIEKYAALLSE 319


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: 267
Number of extensions: 14
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: 321
Length adjustment: 29
Effective length of query: 372
Effective length of database: 292
Effective search space:   108624
Effective search space used:   108624
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