GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Bacteroides thetaiotaomicron VPI-5482

Align candidate 349777 BT0249 (5-methyltetrahydrofolate--homocysteine methyltransferase or methionine synthase (NCBI ptt file))
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.27873.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                          -----------
   1.8e-103  331.8   0.0     2e-103  331.6   0.0    1.0  1  lcl|FitnessBrowser__Btheta:349777  BT0249 5-methyltetrahydrofolate-


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__Btheta:349777  BT0249 5-methyltetrahydrofolate--homocysteine methyltransferase or methionine synt
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  331.6   0.0    2e-103    2e-103       2     273 .]       7     285 ..       6     285 .. 0.98

  Alignments for each domain:
  == domain 1  score: 331.6 bits;  conditional E-value: 2e-103
                       Met_synt_B12   2 leelveyidWtpffqaWelkgkypkile..................dekvgeeakklfkdAqamLkkiieekllka 59 
                                        ++++++yi+W +ff+aW+++ ++++i++                  d+++++ea++lfk+A++mL+ + ++   ++
  lcl|FitnessBrowser__Btheta:349777   7 IHNVAPYINWIYFFHAWGFQPRFAAIANihgcdvcraswlttfpeeDRNKASEAMQLFKEANRMLDLLDKDY--EV 80 
                                        899****************************************************************98877..99 PP

                       Met_synt_B12  60 kavvglfpAnsegddievyadesrseelatlhtLrqqaekeegkpnlclaDfvapkesgvkDyiGlFavtaglgie 135
                                        + +++l++Ans+gd++++   e+++++  ++++Lrqq+ k++g+p +cl+Df++p +sg+ D+iG+Fa ++++++e
  lcl|FitnessBrowser__Btheta:349777  81 RTIFKLCKANSDGDNLVI---EKETDQFLVFPLLRQQTPKRDGSPFFCLSDFIRPLSSGIPDTIGAFASCIDADME 153
                                        ******************...56667899*********************************************** PP

                       Met_synt_B12 136 elakefeaekddYsailvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRpApGYpacpdht 211
                                         l++     +d Y+++lv++l+drLaeA++e++he vrke Wgyakde ls+ +l+ ekYqgiRpA+GYp++pd++
  lcl|FitnessBrowser__Btheta:349777 154 GLYE-----QDPYKHLLVQTLSDRLAEAATEKMHEYVRKEAWGYAKDEILSMPDLLVEKYQGIRPAVGYPSLPDQS 224
                                        **98.....7****************************************************************** PP

                       Met_synt_B12 212 ekktlfelldaeekigieLteslamtPaasvsGlyfahpearyFavgkiekdqvedyakrkg 273
                                         ++ l elld+++ igi+Lte+ am+P+asv+Gl+fahp+a+yF+vgki++dq+edya+r+g
  lcl|FitnessBrowser__Btheta:349777 225 INFLLDELLDMKQ-IGITLTENGAMYPHASVCGLMFAHPAAEYFSVGKIGEDQLEDYARRRG 285
                                        *************.**********************************************97 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (300 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 0.01s 00:00:00.02 Elapsed: 00:00:00.00
# Mc/sec: 8.21
//
[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