GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Cupriavidus basilensis 4G11

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate RR42_RS01160 RR42_RS01160 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>FitnessBrowser__Cup4G11:RR42_RS01160
          Length = 390

 Score =  268 bits (684), Expect = 2e-76
 Identities = 155/357 (43%), Positives = 206/357 (57%), Gaps = 9/357 (2%)

Query: 2   PDARRFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMA- 60
           P    F E   P+++  G  L    +  ET+G L     NA+L+   L+ S H A     
Sbjct: 23  PQCMHFTE---PLKLRNGTSLADYDLMVETYGTLNAARSNAVLVCHALNASHHVAGVYEH 79

Query: 61  DPSP-GWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSV 119
           DP   GWW+ M+GPGKP+DT+RFFVI +N+LGSCFGSTGP S NPATGQPY   FP ++V
Sbjct: 80  DPRDVGWWDNMVGPGKPLDTDRFFVIGVNNLGSCFGSTGPMSANPATGQPYGATFPVVTV 139

Query: 120 EDIVAAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTI 179
           ED V A        GI     V G SLGGM ALA+++MYP   R  I +++    +   I
Sbjct: 140 EDWVNAQARVADRFGITQFAAVMGGSLGGMQALAWSLMYPDRLRHCIVVASTPKLSAQNI 199

Query: 180 ALRSIQREAVRADPAWAGGN-YAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEG 238
           A   + R A+ +DP + GGN YA G  PK G+RVAR +G +TY S E+  ++F RE    
Sbjct: 200 AFNEVARSAILSDPDFHGGNYYAHGVKPKRGLRVARMIGHITYLSDEDMAEKFGREL--K 257

Query: 239 SDDSANPFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRR 298
           +DD    F + FQV+SY+     KFA+ FDAN YL +++A+D FD A    G L  AV +
Sbjct: 258 TDDIRFSFDVEFQVESYLRYQGDKFAEYFDANTYLLITRALDYFDPALAFGGDLTRAVSQ 317

Query: 299 IDAKRALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERF 355
             A   LVA  TTDW F   + R++ + L      VSY E+ +  GHDAFL+D  R+
Sbjct: 318 TQAS-FLVASFTTDWRFAPNRSRELVKALLDNKRPVSYAEIDAPHGHDAFLLDDPRY 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: 395
Number of extensions: 15
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: 390
Length adjustment: 30
Effective length of query: 337
Effective length of database: 360
Effective search space:   121320
Effective search space used:   121320
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.

Links

Downloads

Related tools

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