GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Sphingomonas koreensis DSMZ 15582

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate Ga0059261_2301 Ga0059261_2301 homoserine O-acetyltransferase (EC 2.3.1.31)

Query= SwissProt::S2KHP1
         (367 letters)



>FitnessBrowser__Korea:Ga0059261_2301
          Length = 371

 Score =  280 bits (717), Expect = 3e-80
 Identities = 149/359 (41%), Positives = 208/359 (57%), Gaps = 3/359 (0%)

Query: 6   RFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSM-ADPSP 64
           R + LPGP+R+  G  L  V IAYET+G L   G NA+L+   L+   H AS       P
Sbjct: 11  RHVTLPGPLRLDGGVLLSPVEIAYETYGTLAPDGGNAILICHALTGDQHVASPHPVTGKP 70

Query: 65  GWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVA 124
           GWW  M+GPGKP+D +R F++  N LGSC GS+GPA++NPATG+P+ +DFP +++ D+V 
Sbjct: 71  GWWTRMVGPGKPVDPDRHFIVCANVLGSCMGSSGPATVNPATGRPWGMDFPVITIRDMVR 130

Query: 125 AARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSI 184
           A       LG+  +  V G S+GGM AL++   +P     ++ I++ A  +   IA   +
Sbjct: 131 AQAMLLDHLGVGRLKAVVGGSMGGMQALSWPATFPDRVDAVVVIASTARHSAQNIAFHEV 190

Query: 185 QREAVRADPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSAN 244
            R+AV ADP W GG Y  G+ P  G+ VAR    +TY S     ++F R RL+  +  + 
Sbjct: 191 GRQAVMADPRWNGGAYYDGDPPAAGLAVARMAAHITYLSEAGLTEKFGR-RLQAREAKSF 249

Query: 245 PFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRA 304
            F   FQ++SY+      F DRFDAN YLY+++AMD FD+AE   G L  A R   A+  
Sbjct: 250 GFDADFQIESYLRHQGLSFVDRFDANAYLYITRAMDYFDLAEEHGGLLANAFRETRARFC 309

Query: 305 LVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363
           LV+   TDWL+P    R +   L  AG  VS+ EL S  GHDAFL+++     +V  FL
Sbjct: 310 LVS-FDTDWLYPTRDSRAIVHALNAAGAPVSFVELSSPFGHDAFLLEAPELNRVVDGFL 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: 441
Number of extensions: 28
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: 371
Length adjustment: 30
Effective length of query: 337
Effective length of database: 341
Effective search space:   114917
Effective search space used:   114917
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 09 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