Alignments for a candidate for B12-reactivation-domain in Teredinibacter turnerae T7901

GapMind for Amino acid biosynthesis

Alignments for a candidate for B12-reactivation-domain in Teredinibacter turnerae T7901

Align candidate WP_015817782.1 TERTU_RS09440 (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.4072.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
   8.2e-124  398.5   0.0   1.4e-123  397.7   0.0    1.4  1  lcl|NCBI__GCF_000023025.1:WP_015817782.1  TERTU_RS09440 methionine synthas


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_000023025.1:WP_015817782.1  TERTU_RS09440 methionine synthase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  397.7   0.0  1.4e-123  1.4e-123       2     273 .]     942    1211 ..     941    1211 .. 0.97

  Alignments for each domain:
  == domain 1  score: 397.7 bits;  conditional E-value: 1.4e-123
                              Met_synt_B12    2 leelveyidWtpffqaWelkgkypkiledekvgeeakklfkdAqamLkkiieekllkakavvglfpA 68  
                                                l+elveyidWtpff +W+l gk+p+il+d++vge+a++l++dA+a+L++i++ kll+aka++g+++A
  lcl|NCBI__GCF_000023025.1:WP_015817782.1  942 LTELVEYIDWTPFFITWDLVGKFPAILTDKVVGEAATSLYQDARALLQDIVDGKLLQAKAILGFWEA 1008
                                                89***************************************************************** PP

                              Met_synt_B12   69 nse.gddievyadesrseelatlhtLrqqaeke.egkpnlclaDfvapkesgvkDyiGlFavtaglg 133 
                                                n++ +ddi+++   +++e +atlh++rqq  k+ ++k+ l+laDf+ap+esgv+D +G+F vtag+g
  lcl|NCBI__GCF_000023025.1:WP_015817782.1 1009 NTVdHDDIVLT---HNAEPIATLHHIRQQVIKNdNDKHLLSLADFIAPQESGVTDFVGGFSVTAGIG 1072
                                                **95699**95...556799*********98884666779*************************** PP

                              Met_synt_B12  134 ieelakefeaekddYsailvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRp 200 
                                                ++ela++++a+ ddY+ai+vkaladrLaeAfae+lhe+vrke+Wgy + e+l+++eli+ekY+giRp
  lcl|NCBI__GCF_000023025.1:WP_015817782.1 1073 ADELAASYQAKGDDYNAIMVKALADRLAEAFAEHLHERVRKEFWGYDSAEALDKDELIREKYRGIRP 1139
                                                ******************************************************************* PP

                              Met_synt_B12  201 ApGYpacpdhtekktlfelldaeekigieLteslamtPaasvsGlyfahpearyFavgkiekdqved 267 
                                                ApGYpacpdhtek+tlf+ll+a++ ig++Lte++am PaasvsG+yf+hpe++yF+vgki++dqve+
  lcl|NCBI__GCF_000023025.1:WP_015817782.1 1140 APGYPACPDHTEKATLFKLLQADR-IGVSLTEHYAMFPAASVSGWYFSHPESQYFNVGKISRDQVES 1205
                                                ***********************9.****************************************** PP

                              Met_synt_B12  268 yakrkg 273 
                                                 a+rkg
  lcl|NCBI__GCF_000023025.1:WP_015817782.1 1206 LAERKG 1211
                                                ****97 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (1229 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: 00:00:00.10
# Mc/sec: 3.12
//
[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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer
changes to Amino acid biosynthesis since the publication.

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

GapMind for Amino acid biosynthesis