GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Methylomonas methanica MC09

Align Homoserine O-acetyltransferase; HAT; Homoserine transacetylase; HTA; EC 2.3.1.31 (characterized)
to candidate WP_013817591.1 METME_RS04475 homoserine O-succinyltransferase

Query= SwissProt::P54167
         (301 letters)



>NCBI__GCF_000214665.1:WP_013817591.1
          Length = 355

 Score =  165 bits (418), Expect = 1e-45
 Identities = 115/335 (34%), Positives = 162/335 (48%), Gaps = 42/335 (12%)

Query: 2   PINIPTHLPAKQVLESEHIFVMDESRAFHQDIRPQKIIILNLMPKKI--QTETQLLRLLG 59
           P+   T LP  Q L  E   ++   RA HQ IR   I +LN+MP      TE Q  RL+G
Sbjct: 3   PLVAHTDLPTFQRLHEEGEEILTPDRASHQCIRELHIGLLNIMPDAALEATERQFFRLVG 62

Query: 60  --NSPLQVHFTFLIPSTHTPKNTAREHLDEFYTTFSNIRHKRFDGMIITGAPIEHLAFEE 117
             N   Q H            + AR H+  +Y +F  I+    D +II+GA + H   ++
Sbjct: 63  ACNQIAQFHVHPFTIGGLERNSAARVHIQRYYESFEQIKQDGLDALIISGANVTHDHLQD 122

Query: 118 VSYWEELKEIMEWSKTNVTSTLHICWGAQAGLYYHYGVEKIQMPKKIFGVFEHTVLSKHE 177
            ++WE L E+ EW+K NVTS L  C    A +   YGVE+ ++P+K +GVF H V+ K  
Sbjct: 123 EAFWEPLTEVFEWAKQNVTSVLCSCLATHALIQSCYGVERTRLPEKRWGVFSHKVVDKQH 182

Query: 178 RLVRGFDELYYVPHSRHTDINMEQLQAVPELNILTASKEAGVCLIVSKDE-KQVFLTGHP 236
            L+   +  + VPHSR  ++    ++    L +L AS+EAGV L VS D  + VF  GHP
Sbjct: 183 PLMAEINTRFDVPHSRFNEVFQADMEK-HGLKVLVASEEAGVHLAVSPDGFRIVFFQGHP 241

Query: 237 EYDTNTLLQEYERDLERNLSTVEA-----PKHYF-----------------AKGSNEPVN 274
           EYD  +LL+EY+R++ R  +   A     P HYF                 AK   +P+ 
Sbjct: 242 EYDDISLLKEYKREVLRYYNDERADYPPFPDHYFDAGVQKMLADYAGRVILAKAKGKPLE 301

Query: 275 -------------RWKAHATLLFMNWLNYYVYQET 296
                         W+  A  +F NWL   VYQ T
Sbjct: 302 PLPEAEIIPHLDITWRDSAKAVFNNWLG-KVYQIT 335


Lambda     K      H
   0.320    0.135    0.415 

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: 309
Number of extensions: 17
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: 301
Length of database: 355
Length adjustment: 28
Effective length of query: 273
Effective length of database: 327
Effective search space:    89271
Effective search space used:    89271
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 (21.8 bits)
S2: 48 (23.1 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