GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metZ in Pseudomonas putida KT2440

Align O-succinylhomoserine sulfhydrylase; OSH sulfhydrylase; OSHS sulfhydrylase; EC 2.5.1.- (characterized)
to candidate PP_1308 PP_1308 methionine gamma-lyase

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__Putida:PP_1308
          Length = 398

 Score =  301 bits (772), Expect = 2e-86
 Identities = 156/373 (41%), Positives = 238/373 (63%), Gaps = 6/373 (1%)

Query: 36  HGEAL----FTTSSYVFRTAADAAARFAGEVPGNVYSRYTNPTVRTFEERIAALEGAEQA 91
           HG AL    + T++Y F T    AA FAGE PG+ YSR +NPT+   E+R+A+LEG E  
Sbjct: 24  HGGALVPPVYQTATYAFPTVEYGAACFAGEEPGHFYSRISNPTLALLEQRMASLEGGEAG 83

Query: 92  VATASGMSAILALVMSLCSSGDHVLVSRSVFGSTISLFDKYFKRFGIQVDYPPLSDLAAW 151
           +A ASGM AI + + +L   GD ++V R+++G T +        FG++V +  L+D  A 
Sbjct: 84  LALASGMGAITSTLWTLLRPGDELIVGRTLYGCTFAFLHHGIGEFGVKVRHVDLNDAKAL 143

Query: 152 EAACKPNTKLFFVESPSNPLAELVDIAALAEIAHAKGALLAVDNCFCTPALQQPLKLGAD 211
           +AA    T++ + E+P+NP  +LVDIAA+ E        + VDN +CTP LQ+PL+LGAD
Sbjct: 144 KAAISSKTRMIYFETPANPNMQLVDIAAVVEAVRGHDVHVVVDNTYCTPYLQRPLELGAD 203

Query: 212 VVIHSATKYIDGQGRGMGGVVAGRGEQMKEV--VGFLRTAGPTLSPFNAWLFLKGLETLR 269
           +V+HSATKY+ G G    G+V GR   +  +   G     G  LSP +A L ++G++TL 
Sbjct: 204 LVVHSATKYLSGHGDITAGLVVGRKVLVDRIRLEGLKDMTGAVLSPHDAALLMRGIKTLA 263

Query: 270 IRMQAHSASALALAEWLERQPGIERVYYAGLPSHPQHELARRQQSGFGAVVSFDVKGGRD 329
           +RM  H A+A  +AE+L RQP +E ++Y GLPS  Q+ LA+RQ    G +++F++KGG +
Sbjct: 264 LRMDRHCANAQQVAEFLVRQPQVELIHYPGLPSFAQYALAQRQMRLPGGMIAFELKGGIE 323

Query: 330 AAWRFIDATRMVSITTNLGDTKTTIAHPATTSHGRLSPEDRARAGIGDSLIRVAVGLEDL 389
           A  RF++A ++ +   +LGD ++   HPA+ +H   +P++RA  GI + L+R++VGLED+
Sbjct: 324 AGRRFMNALQLFARAVSLGDAESLAQHPASMTHSSYTPQERAHHGISEGLVRLSVGLEDV 383

Query: 390 DDLKADMARGLAA 402
           +DL AD+ + L A
Sbjct: 384 EDLLADVEQALQA 396


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: 374
Number of extensions: 10
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: 403
Length of database: 398
Length adjustment: 31
Effective length of query: 372
Effective length of database: 367
Effective search space:   136524
Effective search space used:   136524
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