GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Bacteroides thetaiotaomicron VPI-5482

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 352607 BT3080 cysteine synthase A (NCBI ptt file)

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__Btheta:352607
          Length = 315

 Score =  211 bits (538), Expect = 1e-59
 Identities = 127/309 (41%), Positives = 174/309 (56%), Gaps = 15/309 (4%)

Query: 7   LLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQAEADG 66
           L   +GNTPL+ L   +       +G   RL  K+E  NP GS+KDR A+ MIE AE  G
Sbjct: 8   LTDLVGNTPLLELSNYNKS-----NGLKARLIVKIESFNPAGSVKDRVALAMIEDAEMKG 62

Query: 67  LLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIFSAAE 126
           +L PGATI+EPTSGNTG+ LA  A  KGY+LI  MP+  SVERR LL+  GA+++ +   
Sbjct: 63  VLTPGATIIEPTSGNTGVGLAFVAAAKGYKLILTMPDTMSVERRNLLKALGAELVLTPGA 122

Query: 127 GGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLP-EITHFVAGLGT 185
            G   A+A A+EL A  P  V+L Q+ NPAN   H   TG E+  D   ++  FVAG+GT
Sbjct: 123 DGMKGAIAKAEELKAATPGSVILQQFENPANPAMHLRTTGLEIWRDTEGKVDIFVAGVGT 182

Query: 186 TGTLMGTGRFLREHVANVKIVAAEPRYG-------EGVYALRNMDEGFVPELYDPEILTA 238
            GT+ G G  L+    +VK VA EP           G + ++ +  GFVP+ Y+  ++  
Sbjct: 183 GGTISGVGEALKMRDPSVKAVAVEPADSPVLSGGKPGPHKIQGIGAGFVPKTYNASVVDE 242

Query: 239 RYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVADAGW 298
              V   DA+R +R L   EG+  GIS+GA ++AA  +       G+   I  ++ D G 
Sbjct: 243 IIQVQNDDAIRTSRALAEEEGLLVGISSGAAVYAATELAKRPENEGKM--IVALLPDTGE 300

Query: 299 KYLSTGAYA 307
           +YLST  YA
Sbjct: 301 RYLSTILYA 309


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: 280
Number of extensions: 13
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: 323
Length of database: 315
Length adjustment: 28
Effective length of query: 295
Effective length of database: 287
Effective search space:    84665
Effective search space used:    84665
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.

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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