GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Acidovorax sp. GW101-3H11

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 Ac3H11_1975 Cysteine synthase (EC 2.5.1.47)

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1975
          Length = 305

 Score =  204 bits (520), Expect = 2e-57
 Identities = 125/312 (40%), Positives = 170/312 (54%), Gaps = 19/312 (6%)

Query: 3   RYDSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIEQA 62
           + D++LQ +GNTP V + RL         GP   +W K E  NP GSIKDR A+ M+E A
Sbjct: 2   KVDNILQTIGNTPHVRINRLF--------GPGANVWVKSERSNPGGSIKDRIALSMVEDA 53

Query: 63  EADGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQIIF 122
           E  G L+PG TI+EPTSGNTGI LA+ A +KGY+LI VMP++ S+ERR+L+  YGAQ   
Sbjct: 54  EKSGALQPGGTIIEPTSGNTGIGLALVAAVKGYKLILVMPDSMSIERRRLMLAYGAQFDL 113

Query: 123 SAAEGGSNTAVATAKELAATNPSWVMLYQYGNPANTDSHYCGTGPELLADLPE-ITHFVA 181
           +  E G   A+A A+EL A  P   +  Q+ NPAN D H   T  E+LAD PE I   + 
Sbjct: 114 TPREKGMKGAIARAQELQAQTPGSWIPQQFENPANIDVHVRTTAQEILADFPEGIDVLIT 173

Query: 182 GLGTTGTLMGTGRFLREHVANVKIVAAEPRYGEGV-------YALRNMDEGFVPELYDPE 234
           G+GT G + G  + L+     +K+ A EP     +       + ++ +  GF+P+  D  
Sbjct: 174 GVGTGGHITGVAKVLKAKFPQLKVFAVEPTASPVISGGQPSPHPIQGIGAGFIPKNLDTS 233

Query: 235 ILTARYSVGAVDAVRRTRELVHTEGIFAGISTGAVLHAALGVGAGALAAGERADIALVVA 294
           +L     V A  A    R     EG+  GIS+GA L AA+      L AG  A +     
Sbjct: 234 LLDGVIQVDAEPAREFARRAAREEGLLVGISSGATL-AAIAQKLPELPAG--AKVLGFNY 290

Query: 295 DAGWKYLSTGAY 306
           D G +YLS   +
Sbjct: 291 DTGERYLSVEGF 302


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: 295
Number of extensions: 15
Number of successful extensions: 3
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: 305
Length adjustment: 27
Effective length of query: 296
Effective length of database: 278
Effective search space:    82288
Effective search space used:    82288
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