GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Shewanella oneidensis MR-1

Align [CysO sulfur-carrier protein]-thiocarboxylate-dependent cysteine synthase (EC 2.5.1.113); O-phosphoserine sulfhydrylase (EC 2.5.1.65) (characterized)
to candidate 202695 SO3598 cysteine synthase B (NCBI ptt file)

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__MR1:202695
          Length = 288

 Score =  186 bits (471), Expect = 8e-52
 Identities = 108/299 (36%), Positives = 167/299 (55%), Gaps = 19/299 (6%)

Query: 11  LGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEADGLLRP 70
           +G TPLV LQRL        D     +  KLE  NP GS+KDR A+ MI QAE    + P
Sbjct: 7   IGQTPLVRLQRL--------DCGSSTVLLKLEGNNPAGSVKDRAALNMINQAELRQEIAP 58

Query: 71  GATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIF-SAAEGGS 129
           G T++E TSGNTGI+LAMAA +KGY++I +MP N++ ER+  ++ YGA+++     E   
Sbjct: 59  GDTLIEATSGNTGIALAMAAAIKGYKMILIMPSNSTQERKDAMQAYGAELLLVDNMEAAR 118

Query: 130 NTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGLGTTGT 188
           + A+A   E         +L Q+ N  N ++H+  TGPE+      +ITHFV+ +GTTGT
Sbjct: 119 DLALALQAE-----GKGKVLDQFNNQDNANAHFLTTGPEIWQQSQGKITHFVSSMGTTGT 173

Query: 189 LMGTGRFLREHVANVKIVAAEPRYGEGVYALRNMDEGFVPELYDPEILTARYSVGAVDAV 248
           +MG  ++L+    ++ IV  +P  G  +  +R   + ++P ++D   +     +   DA 
Sbjct: 174 IMGVSKYLKSRNPDITIVGLQPADGSSIPGIRRWPQEYLPGIFDAARVDLMMDIEEQDAK 233

Query: 249 RRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVADAGWKYLSTGAYA 307
              R L   EGI AG+S+G  ++AAL +          + +  +V D G +YLS+G ++
Sbjct: 234 AMARALAREEGICAGVSSGGAVYAALELA----RQYPGSVVVAIVCDRGDRYLSSGLFS 288


Lambda     K      H
   0.317    0.134    0.398 

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: 248
Number of extensions: 14
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: 323
Length of database: 288
Length adjustment: 27
Effective length of query: 296
Effective length of database: 261
Effective search space:    77256
Effective search space used:    77256
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: 41 (21.6 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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