GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Caulobacter crescentus NA1000

Align candidate CCNA_02221 CCNA_02221 (methionine synthase I metH)
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.2185.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                             -----------
   1.5e-124  400.9   0.0   2.6e-124  400.1   0.0    1.4  1  lcl|FitnessBrowser__Caulo:CCNA_02221  CCNA_02221 methionine synthase I


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__Caulo:CCNA_02221  CCNA_02221 methionine synthase I metH
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  400.1   0.0  2.6e-124  2.6e-124       2     273 .]     597     872 ..     596     872 .. 0.98

  Alignments for each domain:
  == domain 1  score: 400.1 bits;  conditional E-value: 2.6e-124
                          Met_synt_B12   2 leelveyidWtpffqaWelkgkypkiledekvgeeakklfkdAqamLkkiieekllkakavvglfpAnsegdd 74 
                                           l+elv++idW+pff++Wel g++p+iled++vg++a++l++dA+amL+k++eek++ ak+v+g++pA+++gdd
  lcl|FitnessBrowser__Caulo:CCNA_02221 597 LAELVPFIDWSPFFASWELIGRFPQILEDDVVGQAATDLYRDARAMLDKVVEEKWFGAKGVIGFWPAQAQGDD 669
                                           89*********************************************************************** PP

                          Met_synt_B12  75 ievyadesrseelatlhtLrqqaeke.....egkpnlclaDfvapkesgvkDyiGlFavtaglgieelakefe 142
                                           i++y+de+r +e  +lhtLrqq++k      e k+n++l+Dfvap  +g +Dy+G+Favtag+g +e++++f+
  lcl|FitnessBrowser__Caulo:CCNA_02221 670 IVLYTDETRVAEFSRLHTLRQQMDKGadksgEAKANVALSDFVAPIGQG-ADYVGGFAVTAGHGEDEIVAKFK 741
                                           **********************99886666777899*********9998.7********************** PP

                          Met_synt_B12 143 aekddYsailvkaladrLaeAfaellhekvrkelWgyakdeklsneelikekYqgiRpApGYpacpdhtekkt 215
                                           a+ ddY+ai++ aladrLaeAfae+lh k r elWgya+de+ ++e+li+ekYqgiRpApGYpa+pdhtek t
  lcl|FitnessBrowser__Caulo:CCNA_02221 742 AAGDDYNAIMASALADRLAEAFAEWLHYKARVELWGYAADEDADVERLIAEKYQGIRPAPGYPAQPDHTEKGT 814
                                           ************************************************************************* PP

                          Met_synt_B12 216 lfelldaeekigieLteslamtPaasvsGlyfahpearyFavgkiekdqvedyakrkg 273
                                           lf+lldae+++g++Ltes+amtP a+vsGl+f+h +a+yF+vgki+ dqvedya+rkg
  lcl|FitnessBrowser__Caulo:CCNA_02221 815 LFKLLDAEAATGLQLTESYAMTPGAAVSGLFFSHRQAHYFGVGKIDADQVEDYARRKG 872
                                           ********************************************************97 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (899 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: 00:00:00.00
# Mc/sec: 27.50
//
[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