GapMind for Amino acid biosynthesis

 

Alignments for a candidate for thrC in Desulfotomaculum ruminis DSM 2154

Align Threonine synthase; TS; EC 4.2.3.1 (uncharacterized)
to candidate WP_013840102.1 DESRU_RS00075 threonine synthase

Query= curated2:Q58860
         (405 letters)



>NCBI__GCF_000215085.1:WP_013840102.1
          Length = 402

 Score =  273 bits (699), Expect = 5e-78
 Identities = 143/377 (37%), Positives = 225/377 (59%), Gaps = 3/377 (0%)

Query: 5   CIKCGKTYDVDEIIYTCECGGLLEIIYDYEEIKDKVSEEKLRKREIGVWRYLEYLPVKDE 64
           C KC K Y+ +E+   CECG  L + YD   IK+   +E L+ RE  +WRY E LP+KD+
Sbjct: 9   CSKCNKQYNSEEVHQLCECGAPLIVKYDLARIKENFRKEDLKDREPSLWRYWELLPLKDK 68

Query: 65  SKIVSLCEGGTPLYRCNNLEKELGIKELYVKNEGANPTGSFKDRGMTVGVTRANELGVEV 124
             +VSL EG TP+ +      E+G+  LY+K+EG  P+G+FK RG TVGV+RA ELG++ 
Sbjct: 69  KNLVSLGEGMTPIIKMEVAGPEIGLNNLYLKDEGIIPSGTFKSRGATVGVSRAKELGIKT 128

Query: 125 VGCASTGNTSASLAAYSARSGKKCIVLLPEGKVALGKLAQAMFYGAKVIQVKGNFDDALD 184
           +   + GN  AS + Y AR+G K ++++P+    + +  +    GA +  V G   DA  
Sbjct: 129 LAMPTNGNAGASWSTYGARAGIKSVIVMPQDAPEITR-NECAITGADLYLVDGLISDAGK 187

Query: 185 MVKQLAKEKLIYLLNSI-NPFRLEGQKTIAFEICDQLNWQVPDRVIVPVGNAGNISAIWK 243
           +V +  ++   + ++++  P+R+EG+KT+  EI +Q NW+VPD ++ P G    I  I+K
Sbjct: 188 IVARAVQKYGWFDVSTLKEPYRIEGKKTMGLEIAEQFNWEVPDVILYPTGGGVGIIGIYK 247

Query: 244 GFKEFEITGIIDE-LPKMTGIQADGAKPIVEAFRKRAKDIIPYKNPETIATAIRIGNPVN 302
             +E +  G I E +P++  +QA+G  PIV+A+ ++  +   + N  T A  I +   + 
Sbjct: 248 ALRELQTIGWIGEKMPRLVAVQAEGCAPIVKAWEEKKTESEFWNNASTCAFGITVPKALG 307

Query: 303 APKALDAIYSSGGYAEAVTDEEIVEAQKLLARKEGIFVEPASASSIAGLKKLLEEGIIDR 362
               LDAIY + G A A+ D +++EAQ +LA KEG FV P  AS  +  +KL E+G I  
Sbjct: 308 DFLVLDAIYKTNGCAVAIADNDLLEAQAVLAAKEGTFVCPEGASLYSAARKLREQGWIKE 367

Query: 363 DERIVCITTGHGLKDPD 379
           +E++V + TG GLK P+
Sbjct: 368 NEKVVLLNTGTGLKYPE 384


Lambda     K      H
   0.317    0.137    0.395 

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: 486
Number of extensions: 30
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: 405
Length of database: 402
Length adjustment: 31
Effective length of query: 374
Effective length of database: 371
Effective search space:   138754
Effective search space used:   138754
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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