GapMind for Amino acid biosynthesis

 

Alignments for a candidate for B12-reactivation-domain in Nitratifractor salsuginis DSM 16511

Align candidate WP_013553448.1 NITSA_RS02460 (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.24836.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
    1.6e-36  112.2   0.0    3.2e-36  111.2   0.0    1.5  1  lcl|NCBI__GCF_000186245.1:WP_013553448.1  NITSA_RS02460 methionine synthas


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_000186245.1:WP_013553448.1  NITSA_RS02460 methionine synthase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  111.2   0.0   3.2e-36   3.2e-36       5     257 ..     907    1168 .]     905    1168 .] 0.82

  Alignments for each domain:
  == domain 1  score: 111.2 bits;  conditional E-value: 3.2e-36
                              Met_synt_B12    5 lveyidWtpffqaWelkgky.pkiledekvge.eakklfkdAqamLkkiieekllkakavvglfpAn 69  
                                                l  ++dW    + ++++  y  k +++e++++   k+++   +++ +++ +ekl++   ++g +p++
  lcl|NCBI__GCF_000186245.1:WP_013553448.1  907 LSMIFDWVNKRTLFKMHWGYkSKGMSKEEYQKlLDKTVYPAWERLKDTFLKEKLFEPTILYGYYPCR 973 
                                                56678999988999999888534455555555155566666667777899***************** PP

                              Met_synt_B12   70 segddievyades....rse............elatlhtLrqqaekeegkpnlclaDfvapkesgvk 120 
                                                s+++++ +++ ++    +se             + ++++ rq     ++kp+++l+Df +++   ++
  lcl|NCBI__GCF_000186245.1:WP_013553448.1  974 SDDQELFLFSPDEgwfsESEvnrepleeivgrAVGVFNFPRQ-----RRKPYRALSDFFRHE---RH 1032
                                                **9999999555545431112222333222212333444444.....5789*********95...57 PP

                              Met_synt_B12  121 DyiGlFavtaglgieelakefeaekddYsailvkaladrLaeAfaellhekvrkelWgyakdeklsn 187 
                                                D+++l +v+ag +i e+ +++ ++ +  +  lv+ l   LaeA+ae+ h+++r +l   ++de  + 
  lcl|NCBI__GCF_000186245.1:WP_013553448.1 1033 DVVALTCVSAGPKITEYERALYEKGEYLEYNLVHGLGVELAEALAEVAHKQIRLDLGIASEDEGHTL 1099
                                                *********************9999999999************************999999****** PP

                              Met_synt_B12  188 eelikekYqgiRpApGYpacpdhtekktlfelldaeekigieLteslamtPaasvsGlyfahpeary 254 
                                                +++  ++Y+g R+++GY+acpd ++++ +f+ll+ ee  gieL+e++ ++P++s  ++++ hpea+y
  lcl|NCBI__GCF_000186245.1:WP_013553448.1 1100 RDVRMNRYRGARYSFGYAACPDLEQSRVIFDLLEPEE-FGIELSETFQIHPEQSTTAIVVHHPEATY 1165
                                                *************************************.***************************** PP

                              Met_synt_B12  255 Fav 257 
                                                +av
  lcl|NCBI__GCF_000186245.1:WP_013553448.1 1166 YAV 1168
                                                *97 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (273 nodes)
Target sequences:                          1  (1168 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: 0.02u 0.00s 00:00:00.02 Elapsed: 00:00:00.01
# Mc/sec: 21.04
//
[ok]

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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