GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Methylomonas methanica MC09

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_013818752.1 METME_RS10575 branched-chain-amino-acid transaminase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_000214665.1:WP_013818752.1
          Length = 290

 Score =  113 bits (283), Expect = 5e-30
 Identities = 96/287 (33%), Positives = 137/287 (47%), Gaps = 16/287 (5%)

Query: 7   IAYFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKS 66
           + +     +P   A I V  H L YG   F G+R             FRL RH DRL  S
Sbjct: 6   LCWLNGTLLPLSAASIPVNDHGLLYGDGVFEGIRIYGRRA-------FRLQRHLDRLVLS 58

Query: 67  AKFLHYDI--SAEKIKEVIVDFVKKNQPDKSFYIRPLVYSS--GLGIAPRLHNLEKDFLV 122
           A+ +  +I    + +   I   +     + S YIR +V      LG+ P+        ++
Sbjct: 59  ARAIALNIPYGCDDLTAAIQQLIDAFDAE-SGYIRVMVTRGPGSLGLNPKGCEQPNMIII 117

Query: 123 YG-LEMGDYLAAD-GVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAI 180
              L M D  + + G    ISS  R        R K S  Y+   LAK EA  +G DEA+
Sbjct: 118 ADQLSMVDQTSREQGARLIISSVRRLPADGLDPRIK-SLNYLNHILAKIEANHAGVDEAV 176

Query: 181 LMNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPIDK 240
           L+N+QG+V E T  N+F+VR+  ++TP   +  LEGITR+ IL +A   GI    +P+  
Sbjct: 177 LLNAQGRVAEGTADNIFIVRDACLLTPPCTEGALEGITRELILDLAEAAGIEVRVQPLGV 236

Query: 241 SELMIADEVFLSGTAAKITPVKRIENFTLGG-DRPITEKLRSVLTAV 286
            +L  ADE FL+GT A++ PV  I+   +G    PI  KL+    AV
Sbjct: 237 YDLYAADECFLTGTGAELIPVASIDQRRIGQCPGPIFRKLQQDFAAV 283


Lambda     K      H
   0.320    0.138    0.406 

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: 204
Number of extensions: 10
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: 305
Length of database: 290
Length adjustment: 26
Effective length of query: 279
Effective length of database: 264
Effective search space:    73656
Effective search space used:    73656
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 Jul 25 2024. The underlying query database was built on Jul 25 2024.

Links

Downloads

Related tools

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