GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Desulfuromonas acetexigens DSM 1397

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate WP_276609542.1 BQ4888_RS07655 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_900111775.1:WP_276609542.1
          Length = 366

 Score =  272 bits (695), Expect = 1e-77
 Identities = 147/360 (40%), Positives = 211/360 (58%), Gaps = 6/360 (1%)

Query: 6   RFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMA--DPS 63
           +F E    +R+  G  L  +T+AYET+GEL     N +L+    +  AHAA      D  
Sbjct: 7   QFAEFDVELRLESGRLLGPLTLAYETYGELNADRSNVILVAHAWTGDAHAAGKNTPDDRK 66

Query: 64  PGWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIV 123
           PGWW+ MIGPGK +DT+R+FV+  N +GSC GSTGP S NP TG+PY L FP L V D+V
Sbjct: 67  PGWWDDMIGPGKVLDTDRYFVLCSNVIGSCKGSTGPTSTNPRTGKPYNLTFPVLMVRDMV 126

Query: 124 AAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRS 183
            A +     LGID + TV G S+G M AL ++++YP   R II I+     +P  IAL +
Sbjct: 127 RAQKLLLDRLGIDSLLTVIGGSMGAMQALEWSILYPEMVRSIIPIAGTGRTSPMAIALNA 186

Query: 184 IQREAVRADPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSA 243
           + R+A+  DP W  GNY P   P DG+ + R +G +++ S      +F R R        
Sbjct: 187 LARQAIFNDPLWKKGNYKPEHPPADGLALGRAVGHISFLSDVSMQLKFGR-RFSARHGQF 245

Query: 244 NPFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKR 303
           + F   F+++ Y++ N   F DRFD N +LYL++A+DL+D+A + + SLE A+ ++    
Sbjct: 246 DFFGQ-FEIERYLDYNGASFVDRFDTNAFLYLAKALDLYDVAWNFE-SLEEALDQLRCP- 302

Query: 304 ALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363
           +L    T+DWL+   Q  +V  +L   G  V+YH + S  GHD+FLV+ E+F P V EFL
Sbjct: 303 SLWFAFTSDWLYTPSQTEEVVTVLRKLGKPVAYHLIESDYGHDSFLVEPEKFTPKVVEFL 362


Lambda     K      H
   0.320    0.135    0.414 

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: 374
Number of extensions: 18
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: 367
Length of database: 366
Length adjustment: 30
Effective length of query: 337
Effective length of database: 336
Effective search space:   113232
Effective search space used:   113232
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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