GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Sulfurimonas denitrificans DSM 1251

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_011372396.1 SUDEN_RS03995 homoserine O-acetyltransferase

Query= SwissProt::A0A0I9RJ56
         (370 letters)



>NCBI__GCF_000012965.1:WP_011372396.1
          Length = 369

 Score =  207 bits (528), Expect = 3e-58
 Identities = 124/359 (34%), Positives = 199/359 (55%), Gaps = 9/359 (2%)

Query: 16  SPFPFKRGGALHGARVAYETWGTLAADASNAILIVTGLSPDAHAAA-NDANPAAGWWEGM 74
           +P   + G  L    + YET+G L  D SN I+I   L+   H A   D +  AGWW+ +
Sbjct: 14  NPLYLESGRILEPYDITYETYGELNDDRSNVIVICHALTGSHHCAGIYDGDKKAGWWDSL 73

Query: 75  VGPGKAIDTDRWFVVCVNSLGSCRGSTGPASLNPATGQPYRLDFPELSIEDGARAAIEVV 134
           +G  KA+DTD++FV+C N +GSC GSTGP S       PYR  FP ++I+D  +A I + 
Sbjct: 74  IGSAKAVDTDKYFVICTNVIGSCFGSTGPMSPAHPHHNPYRYKFPVVTIKDMVKAQIILF 133

Query: 135 RAQGIEQLACVVGNSMGGMTALAVLMLHPGIARSHVNISGSAQALPFSIAIRSLQREAIR 194
              GI +   V+G SMGGM AL   + +P  A   + ++ +    P++IA   + +E+I 
Sbjct: 134 DKLGIHKAHAVIGGSMGGMQALLFAIHYPNFASKIITMATTHATQPWAIAFNKVAQESIL 193

Query: 195 LDPRWNGGHYDDDAYPE---SGMRMARKLGVITYRSALEWDGRFGRVRLDSDQTDDDPFG 251
            D  + GG+YD     E   SGM + R  G I++ S      +FGR   ++D    + FG
Sbjct: 194 KDADFKGGYYDSQTIKENGLSGMAVGRMAGYISFLSYESMKNKFGREYKNTDGL-YELFG 252

Query: 252 LEFQVESYLEGHARRFVRFFDPNCYLYLSRSMDWFDLAEYADGDVLAGLAKIRVEKALAI 311
            +FQVE +LE +   F ++FDP  YLY++++++ +D++   D  +   L KI  E  L I
Sbjct: 253 -KFQVELFLEYNGYNFTKWFDPLSYLYITKAINIYDISRGFD-SLKEALKKITCELHL-I 309

Query: 312 GANTDILFPVQQQQQVADGLR-AGGADARFIGLESPQGHDAFLVDFERFCPAVRGFLDA 369
             + D LF   + ++++D L+  G  +  ++ ++S  GHDAFLV+ ++F   ++  LD+
Sbjct: 310 SFSNDQLFKNFEMKEISDALQEIGNTNHSYLDIDSNYGHDAFLVEVDKFEKNIKDMLDS 368


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: 319
Number of extensions: 13
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: 369
Length adjustment: 30
Effective length of query: 340
Effective length of database: 339
Effective search space:   115260
Effective search space used:   115260
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: 49 (23.5 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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