GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hisF in Beijerinckia mobilis UQM 1969

Align imidazole glycerol-phosphate synthase (subunit 2/2) (EC 4.3.2.10) (characterized)
to candidate WP_051955467.1 DL88_RS01890 imidazole glycerol phosphate synthase subunit HisF

Query= BRENDA::Q5NMD6
         (255 letters)



>NCBI__GCF_000745425.1:WP_051955467.1
          Length = 265

 Score =  335 bits (859), Expect = 6e-97
 Identities = 166/250 (66%), Positives = 201/250 (80%), Gaps = 1/250 (0%)

Query: 3   LCTRIIPCLDVADGRVVKGVNFTDLMDAGDPVEQAKVYDAAGADELCFLDISASHEGRGT 62
           L  R+IPCLDV DGRVVKGVNF DL DAGDPV+ A  YDAAGADELCFLDI+ASHE R  
Sbjct: 2   LKARVIPCLDVKDGRVVKGVNFVDLRDAGDPVQCAMAYDAAGADELCFLDITASHEDRSI 61

Query: 63  MLDVVARTAEVCFMPLTVGGGVRQVEDARALLLAGADKVAVNSAAVARPELVAEIADRFG 122
           + DVV RTAE CFMPLTVGGGVR  +D R LLLAGADKV++ SAAV   + V   A++FG
Sbjct: 62  LFDVVERTAEACFMPLTVGGGVRTEDDIRKLLLAGADKVSIMSAAVTDRDFVRRAAEKFG 121

Query: 123 AQCVVAAIDARRNG-DHWEVYTHGGRRPTGINALDHALNLTRLGAGEILLTSMDKDGTRD 181
           +QCVV AIDA+  G   WEV+THGGR+PTGI+A+ +A ++   GAGEILLTSMD+DGT+ 
Sbjct: 122 SQCVVVAIDAKATGPGRWEVFTHGGRKPTGIDAIAYARDVAERGAGEILLTSMDRDGTKA 181

Query: 182 GYDLELTRLVADSVPVPVIASGGVGNLDHMVEGVTKGHASALLAASIFHFGQYSLAEAHE 241
           G+DL LTR VA+SVP+PVIASGGVG LDH+VEG+ +G A A+LAASIFHFG +++AEA +
Sbjct: 182 GFDLALTRAVAESVPIPVIASGGVGTLDHLVEGIAQGGADAVLAASIFHFGTFTIAEAKD 241

Query: 242 ALAKAGLTVR 251
            +A+ GL +R
Sbjct: 242 YMARHGLPMR 251


Lambda     K      H
   0.320    0.136    0.400 

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: 273
Number of extensions: 9
Number of successful extensions: 2
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: 255
Length of database: 265
Length adjustment: 24
Effective length of query: 231
Effective length of database: 241
Effective search space:    55671
Effective search space used:    55671
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 47 (22.7 bits)

Align candidate WP_051955467.1 DL88_RS01890 (imidazole glycerol phosphate synthase subunit HisF)
to HMM TIGR00735 (hisF: imidazoleglycerol phosphate synthase, cyclase subunit)

# 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/TIGR00735.hmm
# target sequence database:        /tmp/gapView.27346.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       TIGR00735  [M=254]
Accession:   TIGR00735
Description: hisF: imidazoleglycerol phosphate synthase, cyclase subunit
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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
   4.6e-110  352.8   0.9   5.1e-110  352.7   0.9    1.0  1  lcl|NCBI__GCF_000745425.1:WP_051955467.1  DL88_RS01890 imidazole glycerol 


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_000745425.1:WP_051955467.1  DL88_RS01890 imidazole glycerol phosphate synthase subunit HisF
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  352.7   0.9  5.1e-110  5.1e-110       1     254 []       1     251 [.       1     251 [. 0.99

  Alignments for each domain:
  == domain 1  score: 352.7 bits;  conditional E-value: 5.1e-110
                                 TIGR00735   1 mlakriipCLdvkdgrvvkGvqfknlrdaGdpvelakkydeeGadelvflditassekretmlevverv 69 
                                               ml  r+ipCLdvkdgrvvkGv+f +lrdaGdpv+ a +yd+ Gadel flditas+e+r+++ +vver+
  lcl|NCBI__GCF_000745425.1:WP_051955467.1   1 MLKARVIPCLDVKDGRVVKGVNFVDLRDAGDPVQCAMAYDAAGADELCFLDITASHEDRSILFDVVERT 69 
                                               7899***************************************************************** PP

                                 TIGR00735  70 aekvfiPltvgGGiksiedvkkllraGadkvsintaavkapelikeladrfGsqaivvaidakreaene 138
                                               ae  f+PltvgGG+++ +d++kll aGadkvsi +aav++ ++++++a++fGsq++vvaidak +    
  lcl|NCBI__GCF_000745425.1:WP_051955467.1  70 AEACFMPLTVGGGVRTEDDIRKLLLAGADKVSIMSAAVTDRDFVRRAAEKFGSQCVVVAIDAKATGP-- 136
                                               ***************************************************************9886.. PP

                                 TIGR00735 139 eakyevtikgGrestdldvvewakeveelGaGeilltsmdkdGtksGydlellkkvkeavkiPviasgG 207
                                                + +ev ++gGr+ t++d++++a++v+e+GaGeilltsmd+dGtk+G+dl+l+++v+e+v iPviasgG
  lcl|NCBI__GCF_000745425.1:WP_051955467.1 137 -GRWEVFTHGGRKPTGIDAIAYARDVAERGAGEILLTSMDRDGTKAGFDLALTRAVAESVPIPVIASGG 204
                                               .69****************************************************************** PP

                                 TIGR00735 208 aGkaehleeaflkgkadaaLaasvfhkreltieevkeylaergvkvr 254
                                               +G+ +hl e++++g ada+Laas+fh++ +ti e k+y+a +g+++r
  lcl|NCBI__GCF_000745425.1:WP_051955467.1 205 VGTLDHLVEGIAQGGADAVLAASIFHFGTFTIAEAKDYMARHGLPMR 251
                                               ********************************************998 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (254 nodes)
Target sequences:                          1  (265 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 0.01s 00:00:00.01 Elapsed: 00:00:00.00
# Mc/sec: 6.85
//
[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:

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