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_086510078.1 BZY95_RS11575 hydroxyectoine utilization dehydratase EutB

Query= SwissProt::Q9WYJ1
         (401 letters)



>NCBI__GCF_002151265.1:WP_086510078.1
          Length = 334

 Score =  230 bits (587), Expect = 4e-65
 Identities = 131/318 (41%), Positives = 193/318 (60%), Gaps = 7/318 (2%)

Query: 2   ITLEDIKEAQRTLKNVVHRTALAYSSVLSEVTGGEIYLKMENLQKTGSFKIRGAYNKIAH 61
           +TL  I +A+R +     RT L  S  LSE    +I LK+E LQ +G+FK+RGA N IA 
Sbjct: 8   VTLASIYQARRRIAGQALRTPLVRSHALSERFDADILLKLETLQPSGAFKLRGAANMIAA 67

Query: 62  LSE----EERKRGVVAASAGNHAQGVALAAQIFGIPATIVMPRYAPLSKITKTRNLGAQV 117
           L E    +  + GVV AS GNH + VA AA   G+PATI + R  P +K+     LGA+V
Sbjct: 68  LIERHGCDALEAGVVTASTGNHGRAVAYAAARLGVPATICLSRLVPANKVAAIEALGAEV 127

Query: 118 ILEGNIFDEAYEAALRIQEKTGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDVEVVVVPVG 177
              G   DEA+    R+  + G   + PF+DP + AGQGTIGLE+MED PD++ V+V + 
Sbjct: 128 RRVGESQDEAFGEVERLIRERGMTLIPPFDDPLIAAGQGTIGLELMEDAPDLDRVIVGLS 187

Query: 178 GGGLISGVSVAIKSMNPEVKVIGVQTENMPSMIASLRRGRAERVEGKPTLAD--GIAVKK 235
           GGGL+ G+  A+K++ PE ++ GV      +M  SL+ GR   VE   +LAD  G  +  
Sbjct: 188 GGGLLGGIGAAVKAIRPEARITGVSLSRGAAMWQSLQAGRPVAVEEVESLADSLGGGIGL 247

Query: 236 PGDLTFELVKKYVDEMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVL-NKLDVKGK 294
               TF LV++ +DE   V+E  IA A++ +LE  K++ EGA AVG+AA+  + ++V+G+
Sbjct: 248 DNRCTFSLVREVMDEHYQVSEAAIAQAMVDILEHEKLLVEGAAAVGLAALAEHGIEVRGQ 307

Query: 295 KVAIVISGGNIDVNMIDR 312
           +VA+++SG  + +  +DR
Sbjct: 308 RVALILSGNGVALETLDR 325


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: 256
Number of extensions: 9
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: 334
Length adjustment: 30
Effective length of query: 371
Effective length of database: 304
Effective search space:   112784
Effective search space used:   112784
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.

Links

Downloads

Related tools

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