GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Chlorobaculum tepidum TLS

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate NP_661505.1 CT0605 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_000006985.1:NP_661505.1
          Length = 356

 Score =  230 bits (587), Expect = 4e-65
 Identities = 128/360 (35%), Positives = 196/360 (54%), Gaps = 23/360 (6%)

Query: 3   DARRFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMADP 62
           D  ++ E   P+++  GGELP V +AY TWG L  +  N +L+   L+ +A A S     
Sbjct: 12  DTTQYFESNEPLQLELGGELPGVRVAYRTWGTLNAEKSNVILVCHALTGNADADS----- 66

Query: 63  SPGWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDI 122
              WW  M G G+  D  R F++  N LGSC+G+TGP S+NP +G+ Y  DFP++++ D+
Sbjct: 67  ---WWCGMFGEGRAFDETRDFIVCSNVLGSCYGTTGPMSVNPLSGRHYGPDFPRITIRDM 123

Query: 123 VAAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALR 182
           V   R   R+LGID +  + GASLGGM  L +  MYP     ++ +  +   + + IA  
Sbjct: 124 VNVQRLLLRSLGIDRIRLIVGASLGGMQVLEWGAMYPEMAGALMPMGVSGRHSAWCIAQS 183

Query: 183 SIQREAVRADPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDS 242
             QR+A+ AD  W  G Y P   P+ G+  AR + + TYR  E + QRF R++ E     
Sbjct: 184 EAQRQAIAADAEWQDGWYDPEVQPRKGLAAARMMAMCTYRCFENYQQRFGRKQREDG--- 240

Query: 243 ANPFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAK 302
                  F+ +SY+     K   RFDAN Y+ L++AMD+ D+   G  S EAA+  +   
Sbjct: 241 ------LFEAESYVRHQGDKLVGRFDANTYITLTRAMDMHDLG-RGRDSYEAALGALKMP 293

Query: 303 RALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEF 362
             +++ + +D L+P  +Q ++A L+  + +      L    GHDAFL+D+E  + MV EF
Sbjct: 294 VEILS-IDSDVLYPRQEQEELARLIPGSRLLF----LDEPYGHDAFLIDTETVSRMVCEF 348


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: 346
Number of extensions: 18
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: 356
Length adjustment: 29
Effective length of query: 338
Effective length of database: 327
Effective search space:   110526
Effective search space used:   110526
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 Apr 10 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