GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Stenotrophomonas chelatiphaga DSM 21508

Align candidate WP_057507948.1 ABB28_RS06945 (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.31293.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
   9.1e-131  421.3   0.0   1.8e-130  420.3   0.0    1.5  1  lcl|NCBI__GCF_001431535.1:WP_057507948.1  ABB28_RS06945 methionine synthas


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_001431535.1:WP_057507948.1  ABB28_RS06945 methionine synthase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  420.3   0.0  1.8e-130  1.8e-130       2     273 .]     608     875 ..     607     875 .. 0.98

  Alignments for each domain:
  == domain 1  score: 420.3 bits;  conditional E-value: 1.8e-130
                              Met_synt_B12   2 leelveyidWtpffqaWelkgkypkiledekvgeeakklfkdAqamLkkiieekllkakavvglfpAns 70 
                                               l+elv+yidWtpffqaWel+gkyp+il+de vg++a++l++dA++mL++i++e++l+a+av+gl+pAns
  lcl|NCBI__GCF_001431535.1:WP_057507948.1 608 LAELVDYIDWTPFFQAWELAGKYPAILTDEIVGSQASELYRDARQMLDRIVKERWLQARAVFGLWPANS 676
                                               89******************************************************************* PP

                              Met_synt_B12  71 egddievyadesrseelatlhtLrqqaekeegkpnlclaDfvapkesgvkDyiGlFavtaglgieelak 139
                                               +gdd+ v     + +  atlh+Lrqq +k++++p +claDf+ap++sg++D+iG+Favtag+gi+++++
  lcl|NCBI__GCF_001431535.1:WP_057507948.1 677 VGDDVRVQ----HPDGEATLHFLRQQVDKPAERPDFCLADFIAPADSGRQDWIGAFAVTAGIGIDAHVA 741
                                               *******5....3345789************************************************** PP

                              Met_synt_B12 140 efeaekddYsailvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRpApGYpacp 208
                                               +fea++ddY+ail+kaladr+aeA+ae+lh++vrke+Wg+a+de+l+n++li+ekY+giRpApGYpacp
  lcl|NCBI__GCF_001431535.1:WP_057507948.1 742 RFEAAHDDYNAILLKALADRFAEALAERLHQRVRKEFWGHANDETLDNDALIAEKYSGIRPAPGYPACP 810
                                               ********************************************************************* PP

                              Met_synt_B12 209 dhtekktlfelldaeekigieLteslamtPaasvsGlyfahpearyFavgkiekdqvedyakrkg 273
                                               +h+ek tlf+llda+ ++g++Ltes+am P+a+vsG+yf+hp+++yF vg+++++qv+dyakrkg
  lcl|NCBI__GCF_001431535.1:WP_057507948.1 811 EHSEKDTLFRLLDAQGNAGMQLTESFAMLPTAAVSGYYFSHPQSQYFVVGRVSREQVTDYAKRKG 875
                                               ***************************************************************97 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (894 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: 17.70
//
[ok]

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