GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cmutase in Geotalea uraniireducens Rf4

Align Chorismate mutase; CM; Monofunctional chorismate mutase AroQ(f); EC 5.4.99.5 (characterized)
to candidate WP_011939353.1 GURA_RS12670 chorismate mutase

Query= SwissProt::Q57696
         (99 letters)



>NCBI__GCF_000016745.1:WP_011939353.1
          Length = 91

 Score = 56.2 bits (134), Expect = 9e-14
 Identities = 27/83 (32%), Positives = 55/83 (66%), Gaps = 7/83 (8%)

Query: 8  IRKKIDEIDNKILKLIAERNSLAKDVAEIKNQLGIPINDPEREKYIYDRIRKLCKEHN-- 65
          +R++ID +D+++L++  ER +LA  + EIK  L +P+ DP REK I+ R+    +E N  
Sbjct: 6  LREQIDNLDSELLRIFNERANLALKIGEIKKGLALPVYDPSREKKIFKRM----QEENPG 61

Query: 66 -VDENIGIKIFQILIEHNKALQK 87
           +D+   +++F+ +I+ ++ L++
Sbjct: 62 PLDDQAIVRLFERVIDESRRLER 84


Lambda     K      H
   0.315    0.136    0.363 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 34
Number of extensions: 3
Number of successful extensions: 1
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 99
Length of database: 91
Length adjustment: 10
Effective length of query: 89
Effective length of database: 81
Effective search space:     7209
Effective search space used:     7209
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 39 (20.6 bits)
S2: 39 (19.6 bits)

Align candidate WP_011939353.1 GURA_RS12670 (chorismate mutase)
to HMM PF01817 (CM_2)

# 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/PF01817.25.hmm
# target sequence database:        /tmp/gapView.2321183.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       CM_2  [M=79]
Accession:   PF01817.25
Description: Chorismate mutase type II
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
    ------- ------ -----    ------- ------ -----   ---- --  --------                             -----------
    2.9e-27   81.2   1.2    3.4e-27   81.0   1.2    1.0  1  NCBI__GCF_000016745.1:WP_011939353.1  


Domain annotation for each sequence (and alignments):
>> NCBI__GCF_000016745.1:WP_011939353.1  
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !   81.0   1.2   3.4e-27   3.4e-27       1      78 [.       7      83 ..       7      84 .. 0.97

  Alignments for each domain:
  == domain 1  score: 81.0 bits;  conditional E-value: 3.4e-27
                                  CM_2  1 RkeIdeiDrelleLlaeRmelakeiaeyKkenglpvldpeReeevlerlre...gaeelgldpeavekifreiis 72
                                          R++Id++D+ell++++eR++la +i+e+Kk   lpv+dp+Re+++++r++e   g+    ld++a+ ++f+++i+
  NCBI__GCF_000016745.1:WP_011939353.1  7 REQIDNLDSELLRIFNERANLALKIGEIKKGLALPVYDPSREKKIFKRMQEenpGP----LDDQAIVRLFERVID 77
                                          9**************************************************87777....*************** PP

                                  CM_2 73 esralQ 78
                                          esr+l+
  NCBI__GCF_000016745.1:WP_011939353.1 78 ESRRLE 83
                                          ****99 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (79 nodes)
Target sequences:                          1  (91 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: 0.00u 0.00s 00:00:00.00 Elapsed: 00:00:00.00
# Mc/sec: 7.52
//
[ok]

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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