GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Marinobacter adhaerens HP15

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate GFF285 HP15_284 homoserine O-acetyltransferase

Query= SwissProt::A0A0I9RJ56
         (370 letters)



>FitnessBrowser__Marino:GFF285
          Length = 382

 Score =  227 bits (578), Expect = 5e-64
 Identities = 135/358 (37%), Positives = 195/358 (54%), Gaps = 10/358 (2%)

Query: 16  SPFPFKRGGALHGARVAYETWGTLAADASNAILIVTGLSPDAHAA----ANDANPAAGWW 71
           +P     G +L    +  ET+GTL ADASNA+LI   LS   HAA    A D  P  GWW
Sbjct: 22  APIDLACGQSLENYDLVVETYGTLNADASNAVLICHALSGHHHAAGYHSAEDRKP--GWW 79

Query: 72  EGMVGPGKAIDTDRWFVVCVNSLGSCRGSTGPASLNPATGQPYRLDFPELSIEDGARAAI 131
           +  +GPGK IDTDR+FVV +N+LG C GSTGP S+NP TG+P+  +FP +++ D  ++  
Sbjct: 80  DSCIGPGKPIDTDRFFVVSLNNLGGCHGSTGPNSINPETGKPFGPEFPVITVGDWVKSQA 139

Query: 132 EVVRAQGIEQLACVVGNSMGGMTALAVLMLHPGIARSHVNISGSAQALPFSIAIRSLQRE 191
            +    GI+  A VVG S+GGM AL   + +P   R  V I+ + +    +IA   + R+
Sbjct: 140 LLADRLGIQCWAAVVGGSLGGMQALQWSLDYPDRLRHAVVIASTPRLTAQNIAFNEVARQ 199

Query: 192 AIRLDPRWNGG-HYDDDAYPESGMRMARKLGVITYRSALEWDGRFGRVRLDSDQTDDDPF 250
           AI  D  ++ G +YD D  P  G+ +AR +G ITY S      +FGR     DQ     +
Sbjct: 200 AITSDREFHDGRYYDFDTVPRRGLMLARMVGHITYLSDASMGEKFGREL--RDQAYKFGY 257

Query: 251 GLEFQVESYLEGHARRFVRFFDPNCYLYLSRSMDWFDLAEYADGDVLAGLAKIRVEKALA 310
             EFQVESYL     RF   FD N YL ++R++D+FD A    GD+   LA    E  L 
Sbjct: 258 DAEFQVESYLRYQGERFSESFDANTYLLMTRALDYFDPAYEFGGDLSKALAAASCE-YLV 316

Query: 311 IGANTDILFPVQQQQQVADGLRAGGADARFIGLESPQGHDAFLVDFERFCPAVRGFLD 368
           +  +TD  F   + +++ + +        +  +++P GHDAFL+   R+      ++D
Sbjct: 317 LSFSTDWRFTPARSEEMVNAMIGARRKVSYAEVDAPWGHDAFLIPTPRYTDIFNAYMD 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: 409
Number of extensions: 20
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: 382
Length adjustment: 30
Effective length of query: 340
Effective length of database: 352
Effective search space:   119680
Effective search space used:   119680
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