GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Pseudomonas putida KT2440

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate PP_5097 PP_5097 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>FitnessBrowser__Putida:PP_5097
          Length = 379

 Score =  256 bits (655), Expect = 5e-73
 Identities = 145/358 (40%), Positives = 207/358 (57%), Gaps = 8/358 (2%)

Query: 1   MPDARRFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMA 60
           +P   RF E   P+ +  G  L S  + YET+G L     NA+L+   LS   HAA   A
Sbjct: 14  VPQTARFDE---PLALACGRSLASYELVYETYGTLNASASNAVLICHALSGHHHAAGYHA 70

Query: 61  --DPSPGWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLS 118
             D  PGWW+  IGPGKPIDT RFFV+++N+LG C GSTGP+S+NPATG+PY  DFP L+
Sbjct: 71  ATDRKPGWWDSCIGPGKPIDTNRFFVVSLNNLGGCNGSTGPSSVNPATGKPYGADFPVLT 130

Query: 119 VEDIVAAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFT 178
           VED V +       LGI     V G SLGGM AL + + YP   R  + I++A   +   
Sbjct: 131 VEDWVHSQVRLGERLGIQQWAAVVGGSLGGMQALQWTISYPERVRHCVDIASAPKLSAQN 190

Query: 179 IALRSIQREAVRADPAWAGGNYA-PGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLE 237
           IA   + R+A+  DP + GG++   G  PK G+ +AR +G +TY S +   ++F RE L+
Sbjct: 191 IAFNEVARQAILTDPEFHGGSFQDQGVIPKRGLMLARMVGHITYLSDDSMGEKFGRE-LK 249

Query: 238 GSDDSANPFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVR 297
               + +  ++ FQV+SY+     +F+ RFDAN YL +++A+D FD A    G L A + 
Sbjct: 250 SDKLNYDFHSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAATHGGDLAATLA 309

Query: 298 RIDAKRALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERF 355
            + A   +++  TTDW F   + R++ + L  A   V Y E+ S  GHDAFL+ + R+
Sbjct: 310 HVTADYCIMS-FTTDWRFSPARSREIVDALMAARKNVCYLEIDSPYGHDAFLIPTPRY 366


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: 387
Number of extensions: 20
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: 379
Length adjustment: 30
Effective length of query: 337
Effective length of database: 349
Effective search space:   117613
Effective search space used:   117613
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 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