GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Pseudomonas stutzeri RCH2

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate GFF279 Psest_0280 homoserine O-acetyltransferase

Query= SwissProt::A0A0I9RJ56
         (370 letters)



>FitnessBrowser__psRCH2:GFF279
          Length = 379

 Score =  240 bits (612), Expect = 5e-68
 Identities = 138/359 (38%), Positives = 207/359 (57%), Gaps = 9/359 (2%)

Query: 17  PFPFKRGGALHGARVAYETWGTLAADASNAILIVTGLSPDAHAAA----NDANPAAGWWE 72
           P     G  L   ++ YET+G L A  SNA+LI   LS   HAA     +D  P  GWW+
Sbjct: 23  PLTLACGRTLADYQLIYETYGELNAARSNAVLICHALSGHHHAAGYHSEDDRKP--GWWD 80

Query: 73  GMVGPGKAIDTDRWFVVCVNSLGSCRGSTGPASLNPATGQPYRLDFPELSIEDGARAAIE 132
             +GPGKAIDT+R+FVV +N+LG C GSTGP+S NPA+G+PY  DFP +++ED   +   
Sbjct: 81  SCIGPGKAIDTNRFFVVSLNNLGGCNGSTGPSSTNPASGKPYGADFPVVTVEDWVHSQAR 140

Query: 133 VVRAQGIEQLACVVGNSMGGMTALAVLMLHPGIARSHVNISGSAQALPFSIAIRSLQREA 192
           +    GI Q A VVG S+GGM AL   + +P   R  + I+ + +    +IA   + R+A
Sbjct: 141 LADRLGIAQWAAVVGGSLGGMQALQWTISYPERVRHCLAIASAPKLSAQNIAFNEVARQA 200

Query: 193 IRLDPRWNGGHYDD-DAYPESGMRMARKLGVITYRSALEWDGRFGRVRLDSDQTDDDPFG 251
           I  DP ++GGH+ +    P+ G+ +AR +G ITY S      +FGR  L S++ + D   
Sbjct: 201 ILSDPEFHGGHFQEMGVIPKRGLMLARMVGHITYLSDDAMGTKFGR-GLKSEKLNYDFNS 259

Query: 252 LEFQVESYLEGHARRFVRFFDPNCYLYLSRSMDWFDLAEYADGDVLAGLAKIRVEKALAI 311
           +EFQVESYL      F   FD N YL +++++D+FD A  A+ D LA   ++       +
Sbjct: 260 VEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAA-ANDDDLAKTFEVAKADFCVM 318

Query: 312 GANTDILFPVQQQQQVADGLRAGGADARFIGLESPQGHDAFLVDFERFCPAVRGFLDAL 370
              TD  F  ++ +++ D L A   +  ++ +++PQGHDAFL+   R+  A RG+++ +
Sbjct: 319 SFTTDWRFSPERSREIVDALLAARKNVCYLEIDAPQGHDAFLIPNPRYLQAFRGYMNRI 377


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: 398
Number of extensions: 25
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: 370
Length of database: 379
Length adjustment: 30
Effective length of query: 340
Effective length of database: 349
Effective search space:   118660
Effective search space used:   118660
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 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