GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Caulobacter crescentus NA1000

Align L-threonine ammonia-lyase; L-serine ammonia-lyase; Threonine dehydratase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate CCNA_03203 CCNA_03203 threo-3-hydroxyaspartate ammonia-lyase

Query= SwissProt::Q9WYJ1
         (401 letters)



>FitnessBrowser__Caulo:CCNA_03203
          Length = 325

 Score =  240 bits (612), Expect = 5e-68
 Identities = 131/319 (41%), Positives = 197/319 (61%), Gaps = 6/319 (1%)

Query: 2   ITLEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAH 61
           ++L DI+ A   LK     T L  S  L++  GG I+LK E LQ+ G+FK RGAYN+++ 
Sbjct: 3   VSLADIQAAAVRLKGSAVETPLIESPALNDRLGGRIFLKPETLQRAGAFKFRGAYNRLSQ 62

Query: 62  LSEEERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQVILEG 121
           LS+EE+ RGVVA S+GNHAQGVALAA++ G+PA IVMP  +P  K+  TR  GA +    
Sbjct: 63  LSDEEKARGVVAFSSGNHAQGVALAARLLGVPALIVMPSDSPSVKVEGTRGFGADIRFYD 122

Query: 122 NIFDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDL----PDVEVVVVPVG 177
              ++    A +I  + G V V  ++DPH+IAGQGT+GLEI+         ++ ++  VG
Sbjct: 123 RFTEDRVAIADQIAAERGCVVVPSYDDPHIIAGQGTVGLEIVAQAAAQGATLDRLICCVG 182

Query: 178 GGGLISGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVE-GKPTLADGIAVKKP 236
           GGGLI+G S A+K+++P  ++ GV+         SL  GR E ++    ++ D +    P
Sbjct: 183 GGGLIAGTSTAVKALSPATEIWGVEPAGFDETRRSLESGRRETIDKDARSICDALLTPIP 242

Query: 237 GDLTFELVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGV-AAVLNKLDVKGKK 295
           GDLT+ + +K +  +VAV + E+A+A+ +     K+V E  G V + AA+  K+DV GK 
Sbjct: 243 GDLTWPINQKNLSGVVAVTDAEVAEAMRYAFSTLKLVVEPGGCVALTAALTGKVDVAGKT 302

Query: 296 VAIVISGGNIDVNMIDRII 314
           VAIV+SGGN+D  +  +++
Sbjct: 303 VAIVLSGGNVDPGLFAQVL 321


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: 289
Number of extensions: 12
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: 325
Length adjustment: 29
Effective length of query: 372
Effective length of database: 296
Effective search space:   110112
Effective search space used:   110112
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