GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Mycolicibacterium vanbaalenii PYR-1

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_011778808.1 MVAN_RS07820 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_000015305.1:WP_011778808.1
          Length = 375

 Score =  214 bits (544), Expect = 4e-60
 Identities = 127/356 (35%), Positives = 192/356 (53%), Gaps = 14/356 (3%)

Query: 12  GPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMAD--PSPGWWEY 69
           GP+ +  G  +  V+IA + WGEL  + DN +++   L+  +H         P+PGWW+ 
Sbjct: 25  GPLTLENGEVIDDVSIAVQRWGELSARRDNVVVVLHALTGDSHITGPAGPDHPTPGWWDG 84

Query: 70  MIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGA 129
           + GPG PIDT+R+  I+ N LG C GSTGP+S+ P  G+ +   FP +S+ D VAA   A
Sbjct: 85  VAGPGAPIDTDRWCAISTNVLGGCRGSTGPSSLAP-DGKAWGSRFPTISIRDQVAADVAA 143

Query: 130 CRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAV 189
               GI  V  V G S+GG  AL + +++P + R  + ++  A AT   I  +  Q  A+
Sbjct: 144 LERFGITEVAAVIGGSMGGARALEWMMLHPDSVRAALVLAVGARATADQIGTQCTQVAAI 203

Query: 190 RADPAWAGGNY-APGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAM 248
           ++DP W GG+Y   G  P  G+ +AR+   LTYR   E  +RF  +   G D +      
Sbjct: 204 KSDPNWRGGDYHGTGRSPDHGLEIARRFAHLTYRGETELDERFGNDAQPGEDPATGG--- 260

Query: 249 AFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAG 308
            + VQSY+E   RK   RFDA  Y+ L+ A+   D+   G G + AA++       +V G
Sbjct: 261 RYSVQSYLEHQGRKLLARFDAGTYVTLTDALSSHDIG-RGRGGVAAALQSCPVP-TVVGG 318

Query: 309 VTTDWLFPLWQQRQVAELLEHA-GVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363
           +T+D L+PL  Q ++AELL    G+ V    + S  GHD FLV+++    ++   L
Sbjct: 319 ITSDRLYPLRLQAELAELLPGCDGLDV----VDSACGHDGFLVETDAVGKLIRRTL 370


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: 462
Number of extensions: 30
Number of successful extensions: 7
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: 375
Length adjustment: 30
Effective length of query: 337
Effective length of database: 345
Effective search space:   116265
Effective search space used:   116265
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