GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Azoarcus sp. BH72

Align candidate WP_011767448.1 AZO_RS18695 (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.17905.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
   3.3e-133  429.3   0.0   5.5e-133  428.6   0.0    1.4  1  lcl|NCBI__GCF_000061505.1:WP_011767448.1  AZO_RS18695 methionine synthase


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_000061505.1:WP_011767448.1  AZO_RS18695 methionine synthase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  428.6   0.0  5.5e-133  5.5e-133       1     273 []     947    1219 ..     947    1219 .. 0.99

  Alignments for each domain:
  == domain 1  score: 428.6 bits;  conditional E-value: 5.5e-133
                              Met_synt_B12    1 dleelveyidWtpffqaWelkgkypkiledekvgeeakklfkdAqamLkkiieekllkakavvglfp 67  
                                                dl+el++yidW pffq+W+l+g++pkil+de+vge+a+++f+dAqamL+++i+ ++++akav+glfp
  lcl|NCBI__GCF_000061505.1:WP_011767448.1  947 DLDELRDYIDWGPFFQTWDLAGSFPKILDDEVVGETARNVFNDAQAMLEDLIAGEWVQAKAVFGLFP 1013
                                                699**************************************************************** PP

                              Met_synt_B12   68 AnsegddievyadesrseelatlhtLrqqaekeegkpnlclaDfvapkesgvkDyiGlFavtaglgi 134 
                                                Ans+gddi  yadesr+e ++t+h Lrqq+e+++gkp+ claDfvapk+sgv+D++G+Favtaglgi
  lcl|NCBI__GCF_000061505.1:WP_011767448.1 1014 ANSVGDDIAFYADESRDEPMMTWHGLRQQHERPAGKPHWCLADFVAPKASGVRDWCGAFAVTAGLGI 1080
                                                ******************************************************************* PP

                              Met_synt_B12  135 eelakefeaekddYsailvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRpA 201 
                                                e++++efea++ddY+ai++k+ladrLaeA+ae+lhe+vrke+Wgya+de+l+n +like+Y+giRpA
  lcl|NCBI__GCF_000061505.1:WP_011767448.1 1081 EHKLAEFEAAHDDYRAIMLKSLADRLAEATAEWLHERVRKEYWGYAADEQLDNAALIKEQYKGIRPA 1147
                                                ******************************************************************* PP

                              Met_synt_B12  202 pGYpacpdhtekktlfelldaeekigieLteslamtPaasvsGlyfahpearyFavgkiekdqvedy 268 
                                                pGYpacpdht k+ lf+llda +++g+ Ltes+amtPaasvsG+yfahpe++yFa+ ki++dqv+d+
  lcl|NCBI__GCF_000061505.1:WP_011767448.1 1148 PGYPACPDHTVKAALFQLLDAPTNAGMGLTESMAMTPAASVSGFYFAHPESHYFAISKIGRDQVTDW 1214
                                                ******************************************************************* PP

                              Met_synt_B12  269 akrkg 273 
                                                a+r g
  lcl|NCBI__GCF_000061505.1:WP_011767448.1 1215 AQRTG 1219
                                                **975 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (1233 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: 20.42
//
[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