GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Dechlorosoma suillum PS

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate Dsui_0741 Dsui_0741 homoserine O-acetyltransferase

Query= SwissProt::Q2T284
         (381 letters)



>FitnessBrowser__PS:Dsui_0741
          Length = 375

 Score =  554 bits (1428), Expect = e-162
 Identities = 266/374 (71%), Positives = 310/374 (82%), Gaps = 5/374 (1%)

Query: 3   SIGVVAPHTMHFAEPLRLQSGSVLGNYQLVVETYGELNAARSNAVLVCHALNASHHVAGV 62
           S+GVV+P   HFAEP++L SG+ L  Y LV ETYG LNA RSNAVLVCHAL+ SHHVAG 
Sbjct: 6   SVGVVSPQRAHFAEPIQLASGATLAAYDLVYETYGRLNADRSNAVLVCHALSGSHHVAGH 65

Query: 63  YADDPRSTGWWDNMVGPGKPLDTNRFFVIGVNNLGSCFGSTGPMSIDPATGTPYGARFPV 122
           YAD+P++ GWWDN+VGPGKPLDT++FFV+GVNNLG C+GSTGP SI+PATG PYGA FPV
Sbjct: 66  YADNPKNVGWWDNLVGPGKPLDTDKFFVVGVNNLGGCYGSTGPGSINPATGKPYGADFPV 125

Query: 123 VTVEDWVHAQARVADAFGIERFAAVMGGSLGGMQALAWSLLYPERVAHCIDIASTPKLSA 182
           VTVEDWV +QAR+AD  GI ++AA++GGSLGGMQAL WSL YPERV H + IAS PKL+A
Sbjct: 126 VTVEDWVESQARLADRLGINQWAAIIGGSLGGMQALQWSLEYPERVRHALVIASAPKLTA 185

Query: 183 QNIAFNEVARSAILSDPDFHGGDYYAHGVKPRRGLRVARMIGHITYLSDDDMAEKFGRAL 242
           QNIAFNEVAR AIL+DPDFHGG+YY HGV P RGLR+ARM+GHITYLSDD M EKFGR L
Sbjct: 186 QNIAFNEVARQAILTDPDFHGGNYYEHGVVPARGLRLARMVGHITYLSDDQMGEKFGRQL 245

Query: 243 RRADGALDAYNFNFDVEFEVESYLRYQGDKFADYFDANTYLLITRALDYFDPAKAFNGNL 302
           R  +G L    +N+DV+FE+ESYLRYQGDKFA +FDANTYL+ T+ALDYFDPA+ F G+L
Sbjct: 246 R--EGVL---KYNYDVDFEIESYLRYQGDKFAGFFDANTYLITTKALDYFDPARDFGGDL 300

Query: 303 SAALAHTKAKYLVASFTTDWRFAPARSREIVKALLDNRRSVSYAEIDAPHGHDAFLLDDA 362
            AALA   AK+L+ SFTTDWRFAP RSRE+V ALL N R VSYAEID   GHD+FLLDDA
Sbjct: 301 KAALARASAKFLLVSFTTDWRFAPERSREMVYALLHNNREVSYAEIDCNAGHDSFLLDDA 360

Query: 363 RYHNLVRAYYERIA 376
           +YH ++ AY   IA
Sbjct: 361 QYHAVMGAYLHNIA 374


Lambda     K      H
   0.322    0.136    0.417 

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: 558
Number of extensions: 14
Number of successful extensions: 2
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: 381
Length of database: 375
Length adjustment: 30
Effective length of query: 351
Effective length of database: 345
Effective search space:   121095
Effective search space used:   121095
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