GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Pseudomonas putida KT2440

Align L-threonine ammonia-lyase; L-serine ammonia-lyase; Threonine dehydratase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate PP_3191 PP_3191 putative threonine ammonia-lyase / dehydratase

Query= SwissProt::Q9WYJ1
         (401 letters)



>FitnessBrowser__Putida:PP_3191
          Length = 350

 Score =  212 bits (540), Expect = 1e-59
 Identities = 125/304 (41%), Positives = 184/304 (60%), Gaps = 4/304 (1%)

Query: 5   EDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAHLSE 64
           ++I++A   L+  V  T L +S  LS +TG E+ LK E+LQ TGSFK RGA NK+  L  
Sbjct: 38  QNIQDAHAALRPAVSITPLLHSPRLSALTGCEVLLKCEHLQHTGSFKFRGASNKMRLLPA 97

Query: 65  EERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVI-LEGNI 123
           E RK+GV+AAS+GNH Q +ALA ++ G+P  +     A   K    R LGA+V+ L  + 
Sbjct: 98  EARKQGVIAASSGNHGQALALAGKMAGVPVKVYTTTGASAYKTEAMRALGAEVVCLPTDP 157

Query: 124 FDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVGGGGLIS 183
                EAA R  +  G  FV P+ND  VIAGQGTIG+E++E  PD++ V V VGGGG+IS
Sbjct: 158 LSAELEAA-RQAKAQGVPFVSPYNDLQVIAGQGTIGMELLEQAPDLDAVFVAVGGGGMIS 216

Query: 184 GVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLADGIA-VKKPGDLTFE 242
           G+  A++ + P  ++IG    N P++  SL+ G    ++   TL+DG A   +PG +TF 
Sbjct: 217 GIGAALRVLKPGTEIIGCWPANDPTLQQSLKAGEIIELDACETLSDGTAGGVEPGSITFP 276

Query: 243 LVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVLNKLD-VKGKKVAIVIS 301
           L +  + + V V+E+EI  A+  +    + + EGA AV VA +    +  +GK+VA+++ 
Sbjct: 277 LCQALLTDTVLVSEDEIRCAMRDIASSERWIIEGAAAVAVAGMQRLAERYQGKRVAVILC 336

Query: 302 GGNI 305
           G NI
Sbjct: 337 GRNI 340


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: 260
Number of extensions: 7
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: 350
Length adjustment: 30
Effective length of query: 371
Effective length of database: 320
Effective search space:   118720
Effective search space used:   118720
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: 50 (23.9 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