GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Pseudomonas simiae WCS417

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate GFF1476 PS417_07505 cysteine synthase

Query= metacyc::MONOMER-20568
         (299 letters)



>FitnessBrowser__WCS417:GFF1476
          Length = 324

 Score =  226 bits (575), Expect = 7e-64
 Identities = 137/314 (43%), Positives = 178/314 (56%), Gaps = 23/314 (7%)

Query: 2   IYDNILETIGNTPLVRINHLNPNPKVQMYAKLEGFNPTGSVKDRIALKMIEQAEAEGKLH 61
           I+ +   +IGNTPLV+IN + P   V + AK+EG NP  SVK RI   MI  AE+ GKL 
Sbjct: 4   IFADNAHSIGNTPLVQINRIAPRG-VTILAKIEGRNPGYSVKCRIGANMIWDAESTGKLK 62

Query: 62  PGSTIIEATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILTDKKLGT 121
           PG TI+E TSGNTGIGLA +   +GY +++ M   +SIERRK++KA GAE++LT+   G 
Sbjct: 63  PGMTIVEPTSGNTGIGLAFVAAARGYKLLLTMPASMSIERRKVLKALGAELVLTEPAKGM 122

Query: 122 DGAIRKVAELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVAAVGTSG 181
            GAI K  E+V  +P  YF P QF N  N   H KTT  EIW  T G V   VA VGT G
Sbjct: 123 KGAIEKAGEIVASDPATYFMPAQFENPANPAIHEKTTGPEIWNDTDGAVDVLVAGVGTGG 182

Query: 182 TLMGVG---KNLREK-------NPEIKIIEAQPTKG-------HYIQGLKSMEEAIVPAI 224
           T+ GV    KN+  K        P +  +  Q   G       H IQG+ +     VP  
Sbjct: 183 TITGVSRYIKNIAGKPILSVAVEPIVSPVITQALAGEEIKPSPHKIQGIGA---GFVPKN 239

Query: 225 YQADKIDEHILIESEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEK--IDSGVIVVL 282
                +D   L+  +E+ A A  ++ +EGI  G+S GAAM  A +LAEK  +    IVV+
Sbjct: 240 LDLSMVDRVELVTDDESKAMALRLMQEEGILCGISCGAAMAVAVRLAEKPEMQGKTIVVI 299

Query: 283 FADRGEKYLSTKLF 296
             D GE+YLS+ LF
Sbjct: 300 LPDSGERYLSSMLF 313


Lambda     K      H
   0.315    0.133    0.367 

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: 278
Number of extensions: 10
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: 299
Length of database: 324
Length adjustment: 27
Effective length of query: 272
Effective length of database: 297
Effective search space:    80784
Effective search space used:    80784
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 48 (23.1 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