GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Paraburkholderia bryophila 376MFSha3.1

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate H281DRAFT_02214 H281DRAFT_02214 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>FitnessBrowser__Burk376:H281DRAFT_02214
          Length = 381

 Score =  270 bits (689), Expect = 6e-77
 Identities = 154/360 (42%), Positives = 210/360 (58%), Gaps = 10/360 (2%)

Query: 2   PDARRFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMAD 61
           P    F E   P+R+  G  L S  +  ET+G L     NA+L+   L+ S H A   AD
Sbjct: 9   PQKMHFTE---PLRLQNGSSLASYDLMVETYGTLNAARSNAVLVCHALNASHHVAGVYAD 65

Query: 62  --PSPGWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSV 119
                GWW+ M+GPGKP+DT +FFVI +N+LGSCFGSTGP SI+PATG PY   FP ++V
Sbjct: 66  NLKDIGWWDNMVGPGKPLDTNKFFVIGVNNLGSCFGSTGPMSIDPATGNPYGATFPVVTV 125

Query: 120 EDIVAAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTI 179
           ED V A        GI     V G SLGGM ALA+++MYP      I +++    +   I
Sbjct: 126 EDWVNAQARVADQFGITRFAAVMGGSLGGMQALAWSMMYPERVGHCIVVASTPKLSAQNI 185

Query: 180 ALRSIQREAVRADPAWAGGN-YAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDR--ERL 236
           A   + R A+ +DP + GGN YA    PK G+RVAR +G +TY S ++  ++F R   R 
Sbjct: 186 AFNEVARSAILSDPDFHGGNYYAHNVKPKRGLRVARMIGHITYLSDDDMAEKFGRSLRRA 245

Query: 237 EGSDDSAN-PFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAA 295
           EG+ D+ N  F + F+V+SY+     KFAD FDAN YL +++A+D FD A+  +G L AA
Sbjct: 246 EGALDAYNFNFDVEFEVESYLRYQGDKFADYFDANTYLLITRALDYFDPAKAFEGDLTAA 305

Query: 296 VRRIDAKRALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERF 355
           V    AK  L+A  TTDW F   + R++ + L      V+Y E+ +  GHDAFL+D  R+
Sbjct: 306 VAHTTAK-YLIASFTTDWRFAPARSRELVKALLDHKRTVTYAEIDAPHGHDAFLLDDARY 364


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: 382
Number of extensions: 17
Number of successful extensions: 5
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: 381
Length adjustment: 30
Effective length of query: 337
Effective length of database: 351
Effective search space:   118287
Effective search space used:   118287
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