GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Halomonas desiderata SP1

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_086510438.1 BZY95_RS13465 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_002151265.1:WP_086510438.1
          Length = 385

 Score =  241 bits (615), Expect = 2e-68
 Identities = 137/355 (38%), Positives = 197/355 (55%), Gaps = 6/355 (1%)

Query: 13  PVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS--SMADPSPGWWEYM 70
           P+ +  G  LP+  + YET+G L  +  NA+L+   LS   HAA      +  PGWW+  
Sbjct: 22  PLALACGRTLPAYDLVYETYGTLNAERSNAVLICHALSGHHHAAGYHDADERKPGWWDAH 81

Query: 71  IGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGAC 130
           IGPGK IDT RFFV+++N+LG C GSTGP S NPATG+ +  DFP ++V D V +     
Sbjct: 82  IGPGKSIDTNRFFVVSLNNLGGCHGSTGPISTNPATGRQWGPDFPMVTVSDWVHSQARLA 141

Query: 131 RALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVR 190
             LGI+      G SLGGM  L +  +YP    + + I+A    +   IA   + R+A+R
Sbjct: 142 DRLGIERFAAAIGGSLGGMQVLQWTRLYPERVANAVIIAATPKLSAQNIAFNEVARQAIR 201

Query: 191 ADPAWAGGNYAP-GEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMA 249
           +DP +  G YA  G  P+ G+++AR +G +TY S +    +F R+    S+D    + + 
Sbjct: 202 SDPDFHDGWYAEHGTAPRRGLKLARMVGHITYLSEDAMGSKFGRDL--RSEDLNFGYDVE 259

Query: 250 FQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGV 309
           FQV+SY+      F+  FDAN YL +++A+D FD A    G L  AV        LV   
Sbjct: 260 FQVESYLRYQGDTFSTAFDANTYLLMTKALDYFDPAAEHGGVLAEAVAPCQGP-FLVVSF 318

Query: 310 TTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFLA 364
           T+DW FP  + R++A  L  AG  VSY  + S  GHDAFL+   R+  + A F++
Sbjct: 319 TSDWRFPPSRSRELANALIRAGKRVSYVNIDSPHGHDAFLLPEPRYQAVFAAFMS 373


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: 414
Number of extensions: 29
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: 385
Length adjustment: 30
Effective length of query: 337
Effective length of database: 355
Effective search space:   119635
Effective search space used:   119635
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: 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