GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Halomonas desiderata SP1

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_086511565.1 BZY95_RS19555 homoserine acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_002151265.1:WP_086511565.1
          Length = 410

 Score =  172 bits (437), Expect = 1e-47
 Identities = 114/357 (31%), Positives = 179/357 (50%), Gaps = 17/357 (4%)

Query: 19  GGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMA--DPSPGWWEYMIGPGKP 76
           G  +  V I +E +G L  + DN +L+    S ++HAA      D +PG+W+ +IGPGKP
Sbjct: 59  GDTIAPVRIGWEAYGTLNEERDNVILITHFFSGTSHAAGRYTEDDAAPGYWDAIIGPGKP 118

Query: 77  IDTERFFVIAINSLGSC------FGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGAC 130
           +DT+ +++I+ ++L +         +TGPA+ NP TG+P+  DFP +++ D V   +   
Sbjct: 119 LDTDEYYIISSDTLVNLNVHDPNVTTTGPATPNPETGEPWGTDFPLVTIRDFVEVQKALL 178

Query: 131 RALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVR 190
            + GI+ +H V G S+G + A  +A  YP     +I +     A P+ +A  S     +R
Sbjct: 179 ESQGIERLHAVMGPSMGALQAYEWASTYPERVERLIPVIGGGVADPWLLATLSAWAAPIR 238

Query: 191 ADPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWL---QRFDRERLEGSDDSANPFA 247
            D  W  G+Y   E P DG+R A +L  L   +A  WL   + FDR   +   D      
Sbjct: 239 LDANWNEGDYYDSEPPLDGLREALKLVTL---NANHWLWANETFDRSWADEDADPTRELD 295

Query: 248 MAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVA 307
             + ++  ++  A   A+  DAN  LYL +A   F +A HG GSLE  + RI+A   L+ 
Sbjct: 296 ARYAIEQTLDDIAAARAELADANHLLYLVKANQSF-IAGHG-GSLEEGLGRIEAP-TLIL 352

Query: 308 GVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFLA 364
               D +F     RQ AEL+E  G  V    L   +GH   ++  ++    +  FLA
Sbjct: 353 YSENDLVFAPEGVRQTAELIEDGGADVELVTLEGKRGHLDGILAIDQAGERIRAFLA 409


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: 404
Number of extensions: 22
Number of successful extensions: 5
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: 410
Length adjustment: 30
Effective length of query: 337
Effective length of database: 380
Effective search space:   128060
Effective search space used:   128060
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