GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysE in Xenophilus azovorans DSM 13620

Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_038202407.1 Q392_RS05130 homoserine O-acetyltransferase

Query= SwissProt::D2Z028
         (374 letters)



>NCBI__GCF_000745855.1:WP_038202407.1
          Length = 374

 Score =  244 bits (622), Expect = 4e-69
 Identities = 147/362 (40%), Positives = 204/362 (56%), Gaps = 12/362 (3%)

Query: 5   IPPASRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASR-- 62
           + P S     P   A+R G +L    +AYET+G+LNA R NAVLV   L+   H A R  
Sbjct: 5   VTPQSMSFAAP--LALRSGASLGDYTLAYETYGTLNAERSNAVLVCHALNASHHVAGRYA 62

Query: 63  PDDPTPGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELS 122
               + GWW+ M+GPGK VDTD + VI +N+LGSC GSTGP   +P TG  Y   FP ++
Sbjct: 63  GQPKSEGWWDNMIGPGKAVDTDRFFVIGINNLGSCFGSTGPMHVNPATGRVYGADFPVVT 122

Query: 123 IEDIADAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFS 182
           +ED  DA A  + ALGI  LA V+G S+GGM AL+   ++PE  R    ++ A +    +
Sbjct: 123 VEDWVDAQARLLDALGIDTLAAVMGGSLGGMQALSWTLQYPERVRHAAVIASAPNLNAEN 182

Query: 183 IAVRSLQREAIRSDPGWLQGH-YDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGR-TRI 240
           IA   + R AI +DP +  GH Y+ G  P+RG+  AR +G +TY S    + +FGR  R 
Sbjct: 183 IAFNEVARRAIVTDPDFHGGHFYEHGVVPKRGLRIARMIGHITYLSDDVMNEKFGRELRE 242

Query: 241 GERRRADQGRFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAP 300
           G  R   Q     EF++ESYL +   +F++ FD N+YL ++ A+D FD    GG GG   
Sbjct: 243 GVVRYTTQ---DVEFQIESYLRYQGDKFSEYFDANTYLLITRALDYFD--PAGGHGGDLA 297

Query: 301 GALSRMRVERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIE 360
            AL+R    + L++   TD  F   + +EI   L      VS+  +D P GHDAFL+D  
Sbjct: 298 AALAR-ATAKFLLVSFSTDWRFSPQRSREIVKALLDNRRSVSYAEIDAPHGHDAFLLDDV 356

Query: 361 RF 362
           R+
Sbjct: 357 RY 358


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: 383
Number of extensions: 16
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: 374
Length adjustment: 30
Effective length of query: 344
Effective length of database: 344
Effective search space:   118336
Effective search space used:   118336
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 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