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_0659 PP_0659 Cystathionine gamma-synthase

Query= SwissProt::P55218
         (403 letters)



>FitnessBrowser__Putida:PP_0659
          Length = 423

 Score =  276 bits (705), Expect = 1e-78
 Identities = 143/344 (41%), Positives = 210/344 (61%)

Query: 60  GEVPGNVYSRYTNPTVRTFEERIAALEGAEQAVATASGMSAILALVMSLCSSGDHVLVSR 119
           G+ PG +YSR +NPTV T E ++A LE AE AVA +SGM+AI A++ +  S+G  V+ +R
Sbjct: 57  GKQPGFIYSRMSNPTVATLEAKLAELEQAESAVAFSSGMAAISAVLHTFLSNGKRVVSTR 116

Query: 120 SVFGSTISLFDKYFKRFGIQVDYPPLSDLAAWEAACKPNTKLFFVESPSNPLAELVDIAA 179
             +G T  +F+++  R G+QV      D  A E        L ++E+P+NP  +++DI  
Sbjct: 117 DSYGGTNKIFEEFLPRMGVQVCLCDTLDTEALEREIAAGCDLLYLETPTNPTLKVLDIRR 176

Query: 180 LAEIAHAKGALLAVDNCFCTPALQQPLKLGADVVIHSATKYIDGQGRGMGGVVAGRGEQM 239
           L+  AH  GAL+  DN F TP  Q PL LG DVV+HSATK++ G G  +GGVV G    M
Sbjct: 177 LSAAAHKVGALVVADNTFATPLNQNPLALGVDVVVHSATKFLSGHGDVLGGVVCGAEALM 236

Query: 240 KEVVGFLRTAGPTLSPFNAWLFLKGLETLRIRMQAHSASALALAEWLERQPGIERVYYAG 299
            +V  +    G  L PF+A+L ++G++TL +R++   ASA+ALA +L  +P +E V Y G
Sbjct: 237 AQVRHYREINGAALDPFSAYLIIRGIKTLAVRLRQQQASAMALAHYLSTEPLVEAVNYPG 296

Query: 300 LPSHPQHELARRQQSGFGAVVSFDVKGGRDAAWRFIDATRMVSITTNLGDTKTTIAHPAT 359
           LP+H  H +A+ Q  GFGA+VSF +KGG     R +   +      NLG  +T      T
Sbjct: 297 LPAHAGHAIAKAQMRGFGAIVSFVLKGGMPTVARLLPRLKYAHRAGNLGAVETIYGPART 356

Query: 360 TSHGRLSPEDRARAGIGDSLIRVAVGLEDLDDLKADMARGLAAL 403
           TSH   + E+R   GI + L+R++VG+E+ DDL AD+A+  A++
Sbjct: 357 TSHVENTLEERLALGISEGLVRISVGIEETDDLLADLAQACASV 400


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: 380
Number of extensions: 11
Number of successful extensions: 1
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: 423
Length adjustment: 31
Effective length of query: 372
Effective length of database: 392
Effective search space:   145824
Effective search space used:   145824
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