GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Methanobacterium lacus AL-21

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_013644807.1 METBO_RS06075 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_000191585.1:WP_013644807.1
          Length = 489

 Score =  268 bits (684), Expect = 3e-76
 Identities = 140/347 (40%), Positives = 206/347 (59%), Gaps = 5/347 (1%)

Query: 19  GGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSM-ADPSPGWWEYMIGPGKPI 77
           G +L +V +AYET+G+L  +  NA+L+   L+  AH A     D  PGWW+ +IGPGK +
Sbjct: 25  GEKLKNVQVAYETYGKLNKEKSNAILVCHALTGDAHVAGWYEGDKKPGWWDVIIGPGKCL 84

Query: 78  DTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGACRALGIDH 137
           DTE++F+I  N +G C GSTGP+SINP T +PY LDFP ++++D+V A +    ++G+  
Sbjct: 85  DTEKYFIICSNVIGGCKGSTGPSSINPETNKPYGLDFPIITIKDMVNAQKKLVNSMGVTQ 144

Query: 138 VHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVRADPAWAG 197
           +  V G S+GGM  L + V YP   R  I I+  A ++P  IA   + R A+ +DP W  
Sbjct: 145 LFAVIGGSMGGMQVLQWCVSYPDMVRSAIPIATTAFSSPQQIAFNEVGRRAIISDPNWNN 204

Query: 198 GNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMAFQVQSYME 257
           G Y   E P +G+ +AR +  +TY S E   Q+F R RL+  +D    F   F+V+SY+ 
Sbjct: 205 GQYYDSEVPTEGLALARMIAHITYLSNESMYQKFGR-RLQDKEDYGFDFETDFEVESYLH 263

Query: 258 ANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGVTTDWLFPL 317
                F  RFDAN YLY+++A+D FD+A  G+GSL      +  K  LV  V +DWL+P 
Sbjct: 264 YQGNSFTKRFDANSYLYITKAVDYFDLA--GEGSLAETFYGLKIK-FLVISVDSDWLYPP 320

Query: 318 WQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFLA 364
              R +   L    + VSY E+ S  GHDAFL+++ +   ++A FL+
Sbjct: 321 SLSRDIVMGLNANDINVSYCEIKSSYGHDAFLIEAGQLNYLIAGFLS 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: 433
Number of extensions: 23
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: 489
Length adjustment: 32
Effective length of query: 335
Effective length of database: 457
Effective search space:   153095
Effective search space used:   153095
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 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