GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Synechococcus elongatus PCC 7942

Align candidate Synpcc7942_1372 Synpcc7942_1372 (methionine synthase (B12-dependent))
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.12002.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
    3.7e-44  137.3   0.0    6.1e-44  136.5   0.0    1.4  1  lcl|FitnessBrowser__SynE:Synpcc7942_1372  Synpcc7942_1372 methionine synth


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__SynE:Synpcc7942_1372  Synpcc7942_1372 methionine synthase (B12-dependent)
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  136.5   0.0   6.1e-44   6.1e-44       3     256 ..     943    1189 ..     941    1190 .] 0.92

  Alignments for each domain:
  == domain 1  score: 136.5 bits;  conditional E-value: 6.1e-44
                              Met_synt_B12    3 eelveyidWtpff.qaWelkgkypkiledekvgeeakklfkdAqamLkkiieekllkakavvglfpA 68  
                                                +e+ +y+d +  f   W++++  ++  ++e  +  a+k+    q+  ++i +e+ll+ + v+g fp+
  lcl|FitnessBrowser__SynE:Synpcc7942_1372  943 AEVFSYLDRQALFvGQWQFRKP-KEQSREEYDAFIAEKVEPILQQWTTRILAEDLLEPQVVYGYFPC 1008
                                                6788899988765258999877.455555666678999999999999******************** PP

                              Met_synt_B12   69 nsegddievyadesrseelatlhtLrqqaekeegkpnlclaDfvapkesgvkDyiGlFavtaglgie 135 
                                                 ++g+ +++++ ++r++ +a++ + rq + +      lc+aDf ap+e g++D++ + avt+g+++ 
  lcl|FitnessBrowser__SynE:Synpcc7942_1372 1009 VAVGNSLQLFDPNDRDRPTARFDFPRQRSLR-----RLCIADFFAPEELGIQDVFPMQAVTVGHKAT 1070
                                                **********9999************99665.....7****************************** PP

                              Met_synt_B12  136 elakefeaekddYsa.ilvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRpA 201 
                                                e+a+++ a  d+Ys+ +  + la +LaeA+ae+ h+++r+e  gy + e  s +++++++Yqg R++
  lcl|FitnessBrowser__SynE:Synpcc7942_1372 1071 EFAAQLFAG-DQYSDyLYFHGLAVQLAEALAEWTHARIRRE-LGYGSLEPESLRDILAQRYQGSRYS 1135
                                                ****99887.99997255799*******************9.6************************ PP

                              Met_synt_B12  202 pGYpacpdhtekktlfelldaeekigieLteslamtPaasvsGlyfahpearyFa 256 
                                                +GYpacp+   ++   ell+a++ ig+++ es  ++P++s  +++  hp+a+yF+
  lcl|FitnessBrowser__SynE:Synpcc7942_1372 1136 FGYPACPNVADSRIQLELLEADR-IGMSMDESEQLYPEQSTTAIVAYHPAAKYFS 1189
                                                **********************9.******************************7 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (1190 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: 27.12
//
[ok]

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

Links

Downloads

Related tools

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