GapMind for Amino acid biosynthesis

 

Alignments for a candidate for trpA in Methylohalobius crimeensis 10Ki

Align Tryptophan synthase alpha chain; EC 4.2.1.20 (characterized, see rationale)
to candidate WP_022949611.1 H035_RS0114095 tryptophan synthase subunit alpha

Query= uniprot:M4NLA4
         (266 letters)



>NCBI__GCF_000421465.1:WP_022949611.1
          Length = 273

 Score =  257 bits (656), Expect = 2e-73
 Identities = 139/267 (52%), Positives = 177/267 (66%), Gaps = 3/267 (1%)

Query: 1   MSRIDRRFAALKAANRTGLIPFVTAGDPSPEHMVALMHALVDAGADLIELGVPFSDPMAD 60
           MSRI   F  LK   R  LIPF+TAGDP PE  V ++HA+  AGAD++ELGVPFSDPMAD
Sbjct: 1   MSRIQTTFENLKREKRKALIPFITAGDPRPEFTVPMLHAMAAAGADILELGVPFSDPMAD 60

Query: 61  GPVIQHASERAIAKGVGLADVLGWVAAFRQHDADTPIVLMGYLNPIETHGYARFAGEAVQ 120
           GPVIQ ASERA+   V L  VL  VA FR+ D  TPIVLMGYLNP+E  GY  FA  A +
Sbjct: 61  GPVIQRASERALTHHVSLHQVLDMVAEFRRRDIQTPIVLMGYLNPLERMGYRAFAEAARK 120

Query: 121 AGVDGVLLVDCPLE--ESAVLQPLRDAGLQRILLAAPTTEPSRMAQLCGSAEGFLYYVSF 178
           AGVDGVL VD P E  E+ +L  L +AG+  I L APT+   R+ +   +  G+LYYVS 
Sbjct: 121 AGVDGVLTVDLPPEEAEAEMLPLLYEAGIDPIFLLAPTSTRGRIEKADAAGRGYLYYVSL 180

Query: 179 AGITGAAHLSTGDIAARVADVRARAKAPVAVGFGIRDAASAKAIAGFADAVVIGSALVDR 238
            G+TGA HL   ++A +V ++RA A+ P+ VGFG+++A +A  +A  ADAVV+GSALV +
Sbjct: 181 KGVTGAGHLDLEEVARKVEEIRAAARLPIGVGFGVKNAETAAKMAQLADAVVVGSALVQK 240

Query: 239 L-AGATDAGEITRRTQAFLAPIRAALD 264
           +   + D   I     A L  +RAA+D
Sbjct: 241 VEENSGDPERIETAIVALLKEMRAAMD 267


Lambda     K      H
   0.322    0.136    0.394 

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: 221
Number of extensions: 7
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: 266
Length of database: 273
Length adjustment: 25
Effective length of query: 241
Effective length of database: 248
Effective search space:    59768
Effective search space used:    59768
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 (21.9 bits)
S2: 47 (22.7 bits)

Align candidate WP_022949611.1 H035_RS0114095 (tryptophan synthase subunit alpha)
to HMM TIGR00262 (trpA: tryptophan synthase, alpha subunit (EC 4.2.1.20))

# 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/TIGR00262.hmm
# target sequence database:        /tmp/gapView.20972.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       TIGR00262  [M=256]
Accession:   TIGR00262
Description: trpA: tryptophan synthase, alpha 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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
    5.6e-79  250.6   0.0    6.5e-79  250.4   0.0    1.0  1  lcl|NCBI__GCF_000421465.1:WP_022949611.1  H035_RS0114095 tryptophan syntha


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_000421465.1:WP_022949611.1  H035_RS0114095 tryptophan synthase subunit alpha
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  250.4   0.0   6.5e-79   6.5e-79       1     256 []       8     263 ..       8     263 .. 0.98

  Alignments for each domain:
  == domain 1  score: 250.4 bits;  conditional E-value: 6.5e-79
                                 TIGR00262   1 fetlkkkeekafvpFvtagdPdleksleiiktlvkaGadalElGvpfsDPlaDGptiqaaelRAlkagv 69 
                                               fe+lk+++ ka++pF+tagdP  e ++ +++ ++ aGad+lElGvpfsDP+aDGp+iq+a+ RAl++ v
  lcl|NCBI__GCF_000421465.1:WP_022949611.1   8 FENLKREKRKALIPFITAGDPRPEFTVPMLHAMAAAGADILELGVPFSDPMADGPVIQRASERALTHHV 76 
                                               899****************************************************************** PP

                                 TIGR00262  70 kvekalellkkvrekasniPivlltyynlifkkgveeFyakakeagvdgvlvaDlPleead.dlleaak 137
                                               +++++l++++++r++ ++ Pivl+ y n++ ++g  +F + a++agvdgvl +DlP eea+ ++l    
  lcl|NCBI__GCF_000421465.1:WP_022949611.1  77 SLHQVLDMVAEFRRRDIQTPIVLMGYLNPLERMGYRAFAEAARKAGVDGVLTVDLPPEEAEaEMLPLLY 145
                                               **********************************************************98736889999 PP

                                 TIGR00262 138 khgvkqiflvaPtaeeerlkkiaekseGfvYlvsvaGvtgarerveeevkelikkvkalskkPvlvGFG 206
                                               + g+++ifl aPt+   r++k +  ++G+ Y vs  Gvtga +   eev + +++++a ++ P+ vGFG
  lcl|NCBI__GCF_000421465.1:WP_022949611.1 146 EAGIDPIFLLAPTSTRGRIEKADAAGRGYLYYVSLKGVTGAGHLDLEEVARKVEEIRAAARLPIGVGFG 214
                                               *******************************************99999********************* PP

                                 TIGR00262 207 iskkeqvkelkelgadgvivGsAlvkiieeklddeekaleeleefvkelk 256
                                               + ++e + ++ +l ad+v+vGsAlv+++ee+ +d+e++  ++ ++ ke++
  lcl|NCBI__GCF_000421465.1:WP_022949611.1 215 VKNAETAAKMAQL-ADAVVVGSALVQKVEENSGDPERIETAIVALLKEMR 263
                                               *************.899***********************9999999885 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (256 nodes)
Target sequences:                          1  (273 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 0.01s 00:00:00.02 Elapsed: 00:00:00.01
# Mc/sec: 6.96
//
[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