GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Pedobacter sp. GW460-11-11-14-LB5

Align Homoserine O-succinyltransferase; HST; EC 2.3.1.46; Homoserine transsuccinylase; HTS (uncharacterized)
to candidate CA265_RS08175 CA265_RS08175 homoserine O-acetyltransferase

Query= curated2:A1SMU5
         (369 letters)



>FitnessBrowser__Pedo557:CA265_RS08175
          Length = 352

 Score =  186 bits (471), Expect = 1e-51
 Identities = 107/346 (30%), Positives = 179/346 (51%), Gaps = 24/346 (6%)

Query: 24  LRGGGRLDHVEVAYETYGSLSPARDNAVFICHALTGDAHAAGLHVGSKKRGWWDNLIGPG 83
           L  G ++ ++++AY+TYG L+  +DN +++CHALT +A             WW+ L G  
Sbjct: 15  LESGKKIRNLQIAYQTYGKLNANKDNVIWVCHALTANADVFE---------WWEGLFGQN 65

Query: 84  KPVDTDRFFVISANLLGGCSGSTGPLSTDPATGAPYCLDFPMLHMSDLVAAHRRLVAHLG 143
              + +  +++ AN+LG   GS+ PLST+P TG PY L FP   + DLV+AH+ L +HLG
Sbjct: 66  SLFNPEEHYIVCANVLGSHYGSSNPLSTNPVTGLPYYLSFPQFTIRDLVSAHQLLASHLG 125

Query: 144 IERLHAAVGGSLGGMQVLQWVIDEPDALERAVLVAASSRLSPENIAFSAIGREAIMSDPD 203
           I+ +   +GGSLGG Q ++W I EP+ +E  +L+A ++  SP  IAF+   R AI +D  
Sbjct: 126 IDYIKLLIGGSLGGQQAVEWSISEPNKIENLILIATNAAHSPWGIAFNESQRLAITTDRT 185

Query: 204 FCNGRYVEQGVFPWRGQKVARMMAHITYVSAQSLETKFGHRRRSRGDAWTLGPDYEVEHY 263
           F    Y  Q     +G K AR +A ++Y +  +  +        + D      ++    Y
Sbjct: 186 F----YANQPNGGSKGLKTARSIALLSYRTYSAYGSTQVESVNDKTD------NFRSSSY 235

Query: 264 LQHQGQVFLGRFDALSYLYLTRLLDYFDPFAD-PGTAAALRSTATRFQLTSFDSDWRFDS 322
             +QG+  + RF+A SY YLT+ +D  +   +    A AL+       +   ++D  F  
Sbjct: 236 QNYQGEKLINRFNAYSYYYLTKAMDSHNVGRNRKSIADALKLITANTLVIGIENDVLFPL 295

Query: 323 TQSARMTAELKALGVAVDWAELASPFGHDSFLLQPPGYHERIAEFL 368
           ++   +   +       +++ L S +GHD FL++       I  F+
Sbjct: 296 SEQKYLADHIP----GAEFSALHSDYGHDGFLIETDALTNVIGNFI 337


Lambda     K      H
   0.322    0.138    0.431 

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: 324
Number of extensions: 10
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: 369
Length of database: 352
Length adjustment: 29
Effective length of query: 340
Effective length of database: 323
Effective search space:   109820
Effective search space used:   109820
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 (21.9 bits)
S2: 49 (23.5 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