GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Halomonas desiderata SP1

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_086510351.1 BZY95_RS13015 threonine/serine dehydratase

Query= SwissProt::Q9WYJ1
         (401 letters)



>NCBI__GCF_002151265.1:WP_086510351.1
          Length = 315

 Score =  221 bits (563), Expect = 2e-62
 Identities = 129/307 (42%), Positives = 186/307 (60%), Gaps = 3/307 (0%)

Query: 1   MITLEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIA 60
           M+ LE I+EAQR + + +  T L    VLSE  G  I+LK E  Q+TGSFK RG  N + 
Sbjct: 1   MLPLERIQEAQRRIADSLPPTPLLLDHVLSEKFGRRIWLKGELFQRTGSFKPRGGLNWLR 60

Query: 61  HLSEEERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVILE 120
              EEE   G+ A SAGNHA G+A AA    +P TIVMP  A   K+  +R LGA+VIL 
Sbjct: 61  SAGEEELAGGLGAVSAGNHALGLAWAAGQADVPVTIVMPENASPFKVEGSRKLGAEVILH 120

Query: 121 GNIFDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVGGGG 180
           G+I +EA+E   R+  + G   VHP++D  ++AGQGT+GLEI+E  P+   ++ PVGGGG
Sbjct: 121 GDI-NEAWELMHRLVAERGLTLVHPYDDERIMAGQGTVGLEILEQAPEATAILCPVGGGG 179

Query: 181 LISGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLADGIAVKKPGDLT 240
           LI+G+  A  ++ P + +IGV+     SM A+   G  ER+E   T A  +     G+ T
Sbjct: 180 LIAGIGSAAAALRPGLALIGVEPSGAASMAAAWSAGAPERLERVATCAKSLGAAIVGEHT 239

Query: 241 FELVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVLNKLDVKGKK--VAI 298
           + + ++   +++ V+++ I  A+  LL QAK++AE   AVGVAA+L  L     +  V +
Sbjct: 240 YPVCRETTQKLLQVDDDAIGRAMRHLLYQAKLMAEPGAAVGVAALLEDLVTLPPEGDVVV 299

Query: 299 VISGGNI 305
           VI+GGN+
Sbjct: 300 VITGGNM 306


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: 255
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: 315
Length adjustment: 29
Effective length of query: 372
Effective length of database: 286
Effective search space:   106392
Effective search space used:   106392
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