GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Rhizobium johnstonii 3841

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_011654184.1 RL_RS28060 homoserine O-acetyltransferase

Query= SwissProt::H8L374
         (367 letters)



>NCBI__GCF_000009265.1:WP_011654184.1
          Length = 391

 Score =  173 bits (438), Expect = 8e-48
 Identities = 113/355 (31%), Positives = 185/355 (52%), Gaps = 10/355 (2%)

Query: 18  RGGQ-LQGARLAYETWGRLSPGCDNAVLILTGLSPSAHAAS-HPDGDTSPGWWEGMLGPG 75
           RGG+ +   RL YET+G L+   DNA+LI    S ++HAA  + + D S G+W+ ++G G
Sbjct: 36  RGGRTVPEMRLGYETYGTLNDAKDNAILIPHYFSGNSHAAGKYKEADVSAGYWDAIIGSG 95

Query: 76  KAIDTDRWYVICVNS---LGSDKGS---TGPASPDPATGAPYRLSFPELALEDVASAAHD 129
           K +DTD+++V+ V++   LG++  +   TGPA+ +P TG P+ + FP + + D       
Sbjct: 96  KPVDTDKYFVVSVDTPVNLGANDPNVITTGPATTNPKTGKPWGMDFPIMTIGDFVDTQKG 155

Query: 130 LVKALGIARLACLIGCSMGGMSALAYMLQYEGEVEAHISVDTAPQAQPFAIAIRSLQREA 189
           L++ LGI +   ++G SMGG+ +  +  +Y  ++E  I V ++  A    IA   +    
Sbjct: 156 LMEQLGIGKWHAVMGASMGGLQSYEWAARYPDKLERVIPVISSGWADANLIAWLDVWASP 215

Query: 190 IRLDPNWQDGHYTDAAYPETGMAMARKLGVITYRSAMEWNGRFARIRLDGDQRPDEPFAR 249
           I+LDPNW  G Y     P  G+A A K   +   SA   +G F R        P + +A 
Sbjct: 216 IKLDPNWNGGDYYTGQAPNAGLAQAMKTLTLQANSAEWTDGTFGRDWASEGADPGQSWAN 275

Query: 250 EFQVESYLEHHAQRFVRRFDPACYLYLTRASDWFDVAEYGEGSVMQGLARIHVRRALVIG 309
           +++V + L       V + D   +LYL RA+  F VA   + S+ +GL  I V   ++I 
Sbjct: 276 DYKVVTKLNEAGAARVAQSDANHFLYLARANQLF-VAGQPKDSLYKGLLNIDV-PVMLIY 333

Query: 310 VSTDILFPLEQQQQIAEGLQAAGAEVDFVALDSPQGHDAFLVDIENYSAAIGGFL 364
              D++FP +  +     +++ G  V+FV L+  +GH   L+ I      I  FL
Sbjct: 334 TDEDLIFPGDAVRGTGTIIKSDGTPVEFVELEGTRGHMDGLLSIAQAGERIRAFL 388


Lambda     K      H
   0.320    0.136    0.421 

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: 387
Number of extensions: 19
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 367
Length of database: 391
Length adjustment: 30
Effective length of query: 337
Effective length of database: 361
Effective search space:   121657
Effective search space used:   121657
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 Jul 25 2024. The underlying query database was built on Jul 25 2024.

Links

Downloads

Related tools

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