GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Thermomonospora curvata DSM 43183

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_083789799.1 TCUR_RS07155 homoserine O-acetyltransferase

Query= SwissProt::A0A0I9RJ56
         (370 letters)



>NCBI__GCF_000024385.1:WP_083789799.1
          Length = 385

 Score =  265 bits (678), Expect = 1e-75
 Identities = 156/360 (43%), Positives = 218/360 (60%), Gaps = 16/360 (4%)

Query: 6   PPGTR-FHALPSPFPFKRGGALHGARVAYETWGTLAADASNAILIVTGLSPDAHAA--AN 62
           PPG R +  L  P P + GG L G R+AYETWGT A D SNA+L++  L+ D+HAA  A 
Sbjct: 24  PPGRRQWVTLERPLPLETGGTLPGVRLAYETWGTPAPDGSNAVLVLHALTGDSHAAGPAE 83

Query: 63  DANPAAGWWEGMVGPGKAIDTDRWFVVCVNSLGSCRGSTGPASLNPATGQPYRLDFPELS 122
             +P  GWW+G++GPG+ +DTDR+FVV  N LG C+GSTGPASL P   +P+   FP ++
Sbjct: 84  PGHPTPGWWDGLIGPGRPLDTDRYFVVVPNVLGGCQGSTGPASLRPDGRRPWGGSFPYIT 143

Query: 123 IEDGARAAIEVVRAQGIEQLACVVGNSMGGMTALAVLMLHPGIARSHVNISGSAQALPFS 182
             D   A +++  A GI++ A VVG SMGGM AL   +  P    + + ++ +  A    
Sbjct: 144 QRDQVAAEVQLADALGIDRWALVVGGSMGGMRALEWAVSQPDRVAALLLLATTGAASAEQ 203

Query: 183 IAIRSLQREAIRLDPRWNGGHYDDDA---YPESGMRMARKLGVITYRSALEWDGRFGRVR 239
           IA  + Q +AIR DP + GG Y D A    P +G+ +ARK+  +TYRS  E   RFGR  
Sbjct: 204 IAWANAQIQAIRSDPGFRGGDYYDAAPGQGPHTGLGIARKIAHVTYRSEPELRVRFGR-- 261

Query: 240 LDSDQTDDDPF-GLEFQVESYLEGHARRFVRFFDPNCYLYLSRSMDWFDLAEYADGDVLA 298
               Q D+DPF G  F VESYL+ HA + VR FD N Y+ L+ +M+  D+     G + A
Sbjct: 262 --RPQGDEDPFRGGRFAVESYLDHHADKLVRRFDANSYIVLTETMNGHDVGR-GRGGMAA 318

Query: 299 GLAKIRVEKALAIGANTDILFPVQQQQQVADGLRAGGADARFIGLESPQGHDAFLVDFER 358
            L ++   + L  G ++D L+P+ QQQ++A G+   GAD R   +ESP GHD FL++ E+
Sbjct: 319 ALRRV-TARTLVAGVDSDRLYPLYQQQELAAGI--PGAD-RLRVIESPAGHDGFLIEIEQ 374


Lambda     K      H
   0.322    0.138    0.432 

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: 469
Number of extensions: 34
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: 370
Length of database: 385
Length adjustment: 30
Effective length of query: 340
Effective length of database: 355
Effective search space:   120700
Effective search space used:   120700
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 (21.9 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