GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Sulfuritalea hydrogenivorans sk43H DSM 22779

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_041101080.1 SUTH_RS17455 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_000828635.1:WP_041101080.1
          Length = 372

 Score =  259 bits (662), Expect = 8e-74
 Identities = 143/354 (40%), Positives = 208/354 (58%), Gaps = 6/354 (1%)

Query: 13  PVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS-SMADPSP-GWWEYM 70
           P+ +  GG LP+  + YET+G L     NA+L+   LS   H A  +  +P+  GWW+ +
Sbjct: 17  PLALKGGGLLPAFDLVYETYGTLNAAKSNAILVCHALSGHHHVAGHTEGNPANIGWWDNI 76

Query: 71  IGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGAC 130
           +GPG+P+DTERFF++ +N+LG C GSTGPAS NPATG+P+  DFP ++VED V A     
Sbjct: 77  VGPGRPLDTERFFIVGVNNLGGCHGSTGPASTNPATGKPWGADFPVVTVEDWVDAQARLA 136

Query: 131 RALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVR 190
             LGI     V G SLGGM AL + + +P   R  + I+AA   +   IA   + R+A+ 
Sbjct: 137 DHLGIGAWAAVMGGSLGGMQALQWTLSFPDRVRHALVIAAAPKLSAENIAFNDVARQAIL 196

Query: 191 ADPAWAGGN-YAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMA 249
            DP + GG+ Y  G  P  G+R+AR LG +TY S ++  ++F R    G+   +  F + 
Sbjct: 197 TDPDFHGGHFYEHGVRPVRGLRLARMLGHITYLSDDQMAEKFGRRLRTGA--GSYGFDVE 254

Query: 250 FQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGV 309
           F+++SY+     KFA  FDAN YL +++A+D FD A+  D  L  A+ R  AK  LV   
Sbjct: 255 FEIESYLRYQGDKFAGVFDANTYLRMTKALDYFDPAQDFDDDLARALARARAK-FLVVAF 313

Query: 310 TTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363
           +TDW F   + R++   L H G AV+Y E+ S  GHD+FL+D   +  +V  +L
Sbjct: 314 STDWRFSPERSREIVHALVHNGQAVAYAEIDSAHGHDSFLMDEPHYHAVVDTYL 367


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: 418
Number of extensions: 21
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: 372
Length adjustment: 30
Effective length of query: 337
Effective length of database: 342
Effective search space:   115254
Effective search space used:   115254
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