GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Desulfuromusa kysingii DSM 7343

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_092345255.1 BLU87_RS04830 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_900107645.1:WP_092345255.1
          Length = 370

 Score =  271 bits (692), Expect = 3e-77
 Identities = 141/360 (39%), Positives = 210/360 (58%), Gaps = 6/360 (1%)

Query: 6   RFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS--SMADPS 63
           ++ E    +R+  G  L  +T+AYET+GEL     N +L+    + +AHAA   S  D  
Sbjct: 11  KYAEFDVELRLESGRLLGPLTLAYETYGELNADASNVILVTHAWTGNAHAAGRHSEEDRK 70

Query: 64  PGWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIV 123
           PGWW+ MIGPGK +DT R+F+++ N++GSC GSTGP SINP T +PYRL FP + + D+V
Sbjct: 71  PGWWDNMIGPGKVLDTNRYFILSSNTIGSCKGSTGPTSINPRTRKPYRLSFPVIMIRDMV 130

Query: 124 AAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRS 183
            A +     LGI  +  + G S+G M A+ +A+ YP   R I+ I+      P  IAL +
Sbjct: 131 RAQKLLLDHLGITSLAAIVGGSMGAMQAIEWAIHYPDMVRAIVPIAGTGKTAPMAIALNA 190

Query: 184 IQREAVRADPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSA 243
           + R+A+  DP W  GNY P   P DG  +AR +G +++ S      +F  ER     D  
Sbjct: 191 LARQAIFNDPLWKKGNYQPEHPPADGFSLARAVGHISFLSDISMQLKF--ERRFSVRDGM 248

Query: 244 NPFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKR 303
             F   F+V+ Y++ N + F D+FD N +LYL++A+DL+D+A + D SL  A+ R+    
Sbjct: 249 FDFFGKFEVERYLDYNGKNFVDQFDPNSFLYLAKALDLYDVAWNFD-SLSEALERVQCPS 307

Query: 304 ALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363
              A   +DWL+P  Q  ++ E L+     V YH + S  GHD+FLV+ E++ P++ EFL
Sbjct: 308 IWFA-FNSDWLYPAQQTEELVEELQRLNKTVDYHLIDSDYGHDSFLVEPEKYIPLLKEFL 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: 344
Number of extensions: 14
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: 370
Length adjustment: 30
Effective length of query: 337
Effective length of database: 340
Effective search space:   114580
Effective search space used:   114580
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