GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Xenophilus azovorans DSM 13620

Align candidate WP_084217489.1 Q392_RS29470 (methionine synthase)
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.8821.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
   1.3e-122  394.6   0.0   2.1e-122  393.8   0.0    1.4  1  lcl|NCBI__GCF_000745855.1:WP_084217489.1  Q392_RS29470 methionine synthase


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_000745855.1:WP_084217489.1  Q392_RS29470 methionine synthase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  393.8   0.0  2.1e-122  2.1e-122       1     273 []     624     900 ..     624     900 .. 0.98

  Alignments for each domain:
  == domain 1  score: 393.8 bits;  conditional E-value: 2.1e-122
                              Met_synt_B12   1 dleelveyidWtpffqaWelkgkypkiledekvgeeakklfkdAqamLkkiieekllkakavvglfpAn 69 
                                               dl+el+  idW pffq+W+l+g +p+il+de vg+ea+++f+d+++mL+++ie ++l+a++vvg++pAn
  lcl|NCBI__GCF_000745855.1:WP_084217489.1 624 DLSELAAAIDWGPFFQTWDLAGPFPQILKDEIVGSEAQRVFSDGKRMLQRLIEGRWLTANGVVGFWPAN 692
                                               689****************************************************************** PP

                              Met_synt_B12  70 se.gddievyadesrseelatlhtLrqqaeke....egkpnlclaDfvapkesgvkDyiGlFavtaglg 133
                                               +e +ddi++yade r++++ t++ +rqq+ek+      +pn+claDfvap+++g++Dy+G+Favtag+g
  lcl|NCBI__GCF_000745855.1:WP_084217489.1 693 TEhDDDIVLYADEGRERKVLTWYGMRQQTEKQevngVMRPNRCLADFVAPRDAGIADYVGAFAVTAGIG 761
                                               *94588************************997776789****************************** PP

                              Met_synt_B12 134 ieelakefeaekddYsailvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRpAp 202
                                               +e++ k f ++ ddYsai+ kaladrLaeAfae+lh++vr +lWgya+de+l  e+like+Y+giRpAp
  lcl|NCBI__GCF_000745855.1:WP_084217489.1 762 AEKKEKYFLDDLDDYSAIMFKALADRLAEAFAEVLHRRVRMDLWGYAPDEQLGLEQLIKEQYRGIRPAP 830
                                               ********************************************************************* PP

                              Met_synt_B12 203 GYpacpdhtekktlfelldaeekigieLteslamtPaasvsGlyfahpearyFavgkiekdqvedyakr 271
                                               GYpacpdh+ k  lfell++ee ig+ LteslamtPaasvsG+y+ hpea+yF+vg+i+ dq++d a+r
  lcl|NCBI__GCF_000745855.1:WP_084217489.1 831 GYPACPDHSVKGPLFELLQCEE-IGMGLTESLAMTPAASVSGFYLGHPEAKYFSVGRIGPDQLADLAAR 898
                                               **********************.********************************************** PP

                              Met_synt_B12 272 kg 273
                                               ++
  lcl|NCBI__GCF_000745855.1:WP_084217489.1 899 RQ 900
                                               85 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (914 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: 22.60
//
[ok]

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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