GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Echinicola vietnamensis KMM 6221, DSM 17526

Align candidate Echvi_3638 Echvi_3638 (5-methyltetrahydrofolate--homocysteine methyltransferase)
to HMM PF02965 (Met_synt_B12)

# hmmsearch :: search profile(s) against a sequence database
# HMMER 3.3.1 (Jul 2020); http://hmmer.org/
# Copyright (C) 2020 Howard Hughes Medical Institute.
# Freely distributed under the BSD open source license.
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# query HMM file:                  ../tmp/path.aa/PF02965.21.hmm
# target sequence database:        /tmp/gapView.14253.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       Met_synt_B12  [M=273]
Accession:   PF02965.21
Description: Vitamin B12 dependent methionine synthase, activation domain
Scores for complete sequences (score includes all domains):
   --- full sequence ---   --- best 1 domain ---    -#dom-
    E-value  score  bias    E-value  score  bias    exp  N  Sequence                            Description
    ------- ------ -----    ------- ------ -----   ---- --  --------                            -----------
   2.2e-123  397.1   0.0   4.2e-123  396.1   0.0    1.5  1  lcl|FitnessBrowser__Cola:Echvi_3638  Echvi_3638 5-methyltetrahydrofol


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__Cola:Echvi_3638  Echvi_3638 5-methyltetrahydrofolate--homocysteine methyltransferase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  396.1   0.0  4.2e-123  4.2e-123       1     273 []     609     877 ..     609     877 .. 0.98

  Alignments for each domain:
  == domain 1  score: 396.1 bits;  conditional E-value: 4.2e-123
                         Met_synt_B12   1 dleelveyidWtpffqaWelkgkypkiledekvgeeakklfkdAqamLkkiieekllkakavvglfpAnsegdd 74 
                                          d+++l++yidWtpff++W l+gkypkil+de+vg +a+klf++A+amL+k+i+e++l+akavvgl+p +++gdd
  lcl|FitnessBrowser__Cola:Echvi_3638 609 DIKTLRNYIDWTPFFSTWMLSGKYPKILKDEVVGVQAQKLFDEANAMLDKVIDENWLQAKAVVGLYPVKRSGDD 682
                                          6899********************************************************************** PP

                         Met_synt_B12  75 ievyadesrseelatlhtLrqqaekeegkpnlclaDfvapkesgvkDyiGlFavtaglgieelakefeaekddY 148
                                          + +  de+ +e+ +t+h+Lrqq +k +g pn++laD+++p+   + Dy+G+Favtagl++++++++f+ae ddY
  lcl|FitnessBrowser__Cola:Echvi_3638 683 LAIL-DENLHETGTTFHFLRQQGKKGKGVPNRSLADYLHPE---QVDYFGGFAVTAGLNMDKKVDAFKAEGDDY 752
                                          ***6.99999999***************************5...46**************************** PP

                         Met_synt_B12 149 sailvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRpApGYpacpdhtekktlfellda 222
                                          ++i+ ka+ drLaeA+ae++he vrkelWgya++ekl+n++like+Y giRpApGYpacp+h+ek tlfellda
  lcl|FitnessBrowser__Cola:Echvi_3638 753 NEIMFKAIGDRLAEAAAEYMHEVVRKELWGYAPKEKLENDDLIKESYAGIRPAPGYPACPEHSEKVTLFELLDA 826
                                          ************************************************************************** PP

                         Met_synt_B12 223 eekigieLteslamtPaasvsGlyfahpearyFavgkiekdqvedyakrkg 273
                                          +++i+++Lt+s+am P++svsG+yf hpe+ryF++gki++dqve+yakrkg
  lcl|FitnessBrowser__Cola:Echvi_3638 827 QNSIDVHLTDSFAMLPTSSVSGFYFGHPESRYFGLGKIGEDQVESYAKRKG 877
                                          *************************************************97 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (902 residues searched)
Passed MSV filter:                         1  (1); expected 0.0 (0.02)
Passed bias filter:                        1  (1); expected 0.0 (0.02)
Passed Vit filter:                         1  (1); expected 0.0 (0.001)
Passed Fwd filter:                         1  (1); expected 0.0 (1e-05)
Initial search space (Z):                  1  [actual number of targets]
Domain search space  (domZ):               1  [number of targets reported over threshold]
# CPU time: 0.01u 0.00s 00:00:00.01 Elapsed: 00:00:00.01
# Mc/sec: 21.56
//
[ok]

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