GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metB in Phaeobacter inhibens BS107

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate GFF1919 PGA1_c19510 cys/met metabolism PLP-dependent enzyme

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__Phaeo:GFF1919
          Length = 381

 Score =  168 bits (426), Expect = 2e-46
 Identities = 110/370 (29%), Positives = 184/370 (49%), Gaps = 12/370 (3%)

Query: 34  GEHGEALFTTSSYVFRTAADAAARFAGEVPGNVYSRYTNPTVRTFEERIAALEGAEQAVA 93
           G    A+  +S + F T      RF+G+   ++YSR +NPTVR  E+++A LE  + A+A
Sbjct: 15  GSVAPAIHQSSLFTFPTYDALEERFSGKSEADIYSRTSNPTVRLLEDKLAKLERGDAAIA 74

Query: 94  TASGMSAILALVMSLCSSGDHVLVSRSVFGSTISLFDKYFKRFGIQVDYPPLSDLAAWEA 153
             SGM+AI   V+SL  +GD ++ + + +     LF+    R G+ V Y   +D+     
Sbjct: 75  FGSGMAAISGAVLSLVKAGDRIVSTFNTYSDAYRLFEILMARLGVSVTYVDCNDIDELSN 134

Query: 154 ACKPNTKLFFVESPSNPLAELVDIAALAEIAHAKGALLAVDNCFCTPALQQPLKLGADVV 213
           A     +L F+ESPS+ + E  DI    ++A   G +   DN F +P  Q+PL  GAD+V
Sbjct: 135 AL-VGARLLFLESPSSYVFETCDIKKATDVAKQHGVITIFDNSFASPLGQKPLLHGADIV 193

Query: 214 IHSATKYIDGQGRGMGGVVAGRGEQMKEVVG-FLRTAGPTLSPFNAWLFLKGLETLRIRM 272
           +HS +KY+ G    + G V G  + + ++    L   G  LS   AWL ++GL TL +R+
Sbjct: 194 VHSISKYLSGHSDVVAGCVVGSHDLINQIRDTALPLLGAKLSAMEAWLVIRGLRTLPMRL 253

Query: 273 QAHSASALALAEWLERQPGIERVYYAGLPSHPQHELARRQQSGFGAVVSFDVKGGRDAAW 332
           + H  +A  +   L+    I +++ A +PS           SG G + + ++  G D   
Sbjct: 254 REHQEAADFVVGKLKDDSRIAKIHRA-MPS--------STLSGAGGLFTVELADGLDVR- 303

Query: 333 RFIDATRMVSITTNLGDTKTTIAHPATTSHGRLSPEDRARAGIGDSLIRVAVGLEDLDDL 392
            F DA ++  +  + G  ++     +  +     P    + G+  + IR+  GLE  + L
Sbjct: 304 AFCDALKVFRLGVSWGGFESLALPASVAARIDSGPNALQKFGVSRNAIRLFTGLEGREVL 363

Query: 393 KADMARGLAA 402
            AD+ + L A
Sbjct: 364 LADICQALTA 373


Lambda     K      H
   0.319    0.133    0.392 

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: 299
Number of extensions: 12
Number of successful extensions: 4
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: 403
Length of database: 381
Length adjustment: 31
Effective length of query: 372
Effective length of database: 350
Effective search space:   130200
Effective search space used:   130200
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