GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Dechlorosoma suillum PS

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate Dsui_0741 Dsui_0741 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>FitnessBrowser__PS:Dsui_0741
          Length = 375

 Score =  224 bits (571), Expect = 3e-63
 Identities = 133/355 (37%), Positives = 196/355 (55%), Gaps = 9/355 (2%)

Query: 23  GGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASR-PDDP-TPGWWEAMVGPGKP 80
           G  L    + YET+G LNA R NAVLV   LS   H A    D+P   GWW+ +VGPGKP
Sbjct: 26  GATLAAYDLVYETYGRLNADRSNAVLVCHALSGSHHVAGHYADNPKNVGWWDNLVGPGKP 85

Query: 81  VDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDIADAAAHTVRALGIS 140
           +DTD + V+ VN+LG C GSTGP S +P TG+PY   FP +++ED  ++ A     LGI+
Sbjct: 86  LDTDKFFVVGVNNLGGCYGSTGPGSINPATGKPYGADFPVVTVEDWVESQARLADRLGIN 145

Query: 141 RLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRSLQREAIRSDPGWL 200
           + A ++G S+GGM AL     +PE  R  + ++ A      +IA   + R+AI +DP + 
Sbjct: 146 QWAAIIGGSLGGMQALQWSLEYPERVRHALVIASAPKLTAQNIAFNEVARQAILTDPDFH 205

Query: 201 QG-HYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERRRADQGRFGPEFEVES 259
            G +Y+ G  P RG+  AR +G +TY S  +   +FGR     R    +  +  +FE+ES
Sbjct: 206 GGNYYEHGVVPARGLRLARMVGHITYLSDDQMGEKFGRQL---REGVLKYNYDVDFEIES 262

Query: 260 YLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRMRVERALVMGARTD 319
           YL +   +FA  FD N+YL  + A+D FD       GG    AL+R    + L++   TD
Sbjct: 263 YLRYQGDKFAGFFDANTYLITTKALDYFD--PARDFGGDLKAALARASA-KFLLVSFTTD 319

Query: 320 ILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFGPPVAKFLAIVA 374
             F   + +E+   L     +VS+  +D  AGHD+FL+D  ++   +  +L  +A
Sbjct: 320 WRFAPERSREMVYALLHNNREVSYAEIDCNAGHDSFLLDDAQYHAVMGAYLHNIA 374


Lambda     K      H
   0.321    0.138    0.427 

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: 407
Number of extensions: 18
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: 374
Length of database: 375
Length adjustment: 30
Effective length of query: 344
Effective length of database: 345
Effective search space:   118680
Effective search space used:   118680
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 (21.8 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