GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvA in Stenotrophomonas chelatiphaga DSM 21508

Align threonine deaminase (EC 4.3.1.19) (characterized)
to candidate WP_057509300.1 ABB28_RS14485 threonine dehydratase

Query= reanno::Korea:Ga0059261_3694
         (420 letters)



>NCBI__GCF_001431535.1:WP_057509300.1
          Length = 366

 Score =  215 bits (548), Expect = 2e-60
 Identities = 136/341 (39%), Positives = 190/341 (55%), Gaps = 15/341 (4%)

Query: 6   PMATQAATAAQPLPVTLADVQAAAARIMGAVVHTPTLHSKTLSDLTGATVYLKFENLQFT 65
           P A +A T      VT+ADV AA AR+   +  TP  H++          +LK ENLQ T
Sbjct: 2   PAADRAGTEPDVGDVTVADVLAAQARLRRFLPPTPLHHAERFG------TWLKLENLQRT 55

Query: 66  AAYKERGALNTLLQLDDAARAKGVIAASAGNHAQGLAYHGNRLGIPVTIVMPKSTPTVKV 125
            +YK RGALN LL   +    + +I ASAGNHAQG+A+  +RLG+    VMP   P  K+
Sbjct: 56  GSYKVRGALNALLAGRERGDLRPIICASAGNHAQGVAWAAHRLGVQAITVMPHGAPANKI 115

Query: 126 MQTESHGATIILEGETFDEAYAHARQLEASNGYTFVHPFDDPRIIAGQGTVFLEMLADAP 185
                 GAT+   GE++D+A+A A +L   + Y F+  FDD  +IAGQGTV +E+   +P
Sbjct: 116 AGVAHWGATVRQHGESYDDAWAFAVELAQRHDYRFLSAFDDADVIAGQGTVGIELAPHSP 175

Query: 186 AIDTLIVPIGGGGLISGALTVAKAADKPIEVVGVQAELFPSMFNRFTGAHEPIGG-DTLA 244
             D +IVPIGGGGL SG     K+  + + +VG Q E   SM    +G   PI    +LA
Sbjct: 176 --DVVIVPIGGGGLASGVALALKS--QGVRIVGAQVEGVDSMARAISGDIRPIAPVPSLA 231

Query: 245 EGIAVKEPGGLTAQIVEALVDEIMLVSERSLEEAVSLLLQIEKTVVEGAGAAGLAALMTQ 304
           +G+ VK PG LT ++  +L+D++++V E  L E +  L   E  + EGAGA  LAA    
Sbjct: 232 DGVRVKIPGFLTRRLCASLLDDVVIVREAELRETLVRLALEENLIAEGAGALALAA---- 287

Query: 305 PERFRGKTVGVILTGGNIDTRLLANVLLRDLARSGRLARLR 345
             R  G+    +++GGNID  +LA +L     R+ R  R R
Sbjct: 288 GRRVAGRRKFAVVSGGNIDASVLAGLLTDVRPRAPRKPRRR 328


Lambda     K      H
   0.319    0.135    0.374 

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: 343
Number of extensions: 19
Number of successful extensions: 6
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: 420
Length of database: 366
Length adjustment: 31
Effective length of query: 389
Effective length of database: 335
Effective search space:   130315
Effective search space used:   130315
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 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