GapMind for Amino acid biosynthesis

 

Alignments for a candidate for trpA in Halomonas desiderata SP1

Align Tryptophan synthase alpha chain; EC 4.2.1.20 (characterized, see rationale)
to candidate WP_086508781.1 BZY95_RS04480 tryptophan synthase subunit alpha

Query= uniprot:M4NLA4
         (266 letters)



>NCBI__GCF_002151265.1:WP_086508781.1
          Length = 271

 Score =  277 bits (709), Expect = 1e-79
 Identities = 146/267 (54%), Positives = 180/267 (67%), Gaps = 2/267 (0%)

Query: 1   MSRIDRRFAALKAANRTGLIPFVTAGDPSPEHMVALMHALVDAGADLIELGVPFSDPMAD 60
           M+RID+RFA LKA  R  LIPF+TAGDP+P++ V  MHALV+AGAD+IELGVPFSDPMAD
Sbjct: 1   MNRIDKRFAELKAQGRRALIPFITAGDPAPQYTVGFMHALVEAGADVIELGVPFSDPMAD 60

Query: 61  GPVIQHASERAIAKGVGLADVLGWVAAFRQHDADTPIVLMGYLNPIETHGYARFAGEAVQ 120
           GPVIQ A ERA+   V L  +   V  FRQ D+DTP+VLMGYLNP+E  G   FA +A  
Sbjct: 61  GPVIQKACERALKHNVRLTHLFEMVREFRQRDSDTPVVLMGYLNPVERIGLEAFADQAAA 120

Query: 121 AGVDGVLLVDCPLEESAVLQP-LRDAGLQRILLAAPTTEPSRMAQLCGSAEGFLYYVSFA 179
           AG+DGVL VD P EE+    P L+  GL  I L APTT   R A +C   EG+LYYV+  
Sbjct: 121 AGIDGVLTVDMPPEEADEFGPILKQRGLASIFLVAPTTSSERAATICAHGEGYLYYVALK 180

Query: 180 GITGAAHLSTGDIAARVADVRARAKAPVAVGFGIRDAASAKAIAGFADAVVIGSALVDRL 239
           G+TGAA L+  D+A  +A +R   + P+ VGFGIRD ASA  +   AD V++GSALV R+
Sbjct: 181 GVTGAATLNAADVAEHLAPLRGLTELPLCVGFGIRDGASAAEVGKVADGVIVGSALVSRI 240

Query: 240 AGATDAGE-ITRRTQAFLAPIRAALDA 265
           A   +  E I    +A L  +R ALDA
Sbjct: 241 ADNAERPEAIADELKAVLGEMRQALDA 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: 255
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: 266
Length of database: 271
Length adjustment: 25
Effective length of query: 241
Effective length of database: 246
Effective search space:    59286
Effective search space used:    59286
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_086508781.1 BZY95_RS04480 (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.32325.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
      2e-82  261.9   0.0    2.3e-82  261.7   0.0    1.0  1  lcl|NCBI__GCF_002151265.1:WP_086508781.1  BZY95_RS04480 tryptophan synthas


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_002151265.1:WP_086508781.1  BZY95_RS04480 tryptophan synthase subunit alpha
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  261.7   0.0   2.3e-82   2.3e-82       1     256 []       8     262 ..       8     262 .. 0.99

  Alignments for each domain:
  == domain 1  score: 261.7 bits;  conditional E-value: 2.3e-82
                                 TIGR00262   1 fetlkkkeekafvpFvtagdPdleksleiiktlvkaGadalElGvpfsDPlaDGptiqaaelRAlkagv 69 
                                               f++lk+++ +a++pF+tagdP  + ++ +++ lv+aGad++ElGvpfsDP+aDGp+iq+a  RAlk+ v
  lcl|NCBI__GCF_002151265.1:WP_086508781.1   8 FAELKAQGRRALIPFITAGDPAPQYTVGFMHALVEAGADVIELGVPFSDPMADGPVIQKACERALKHNV 76 
                                               7899***************************************************************** PP

                                 TIGR00262  70 kvekalellkkvrekasniPivlltyynlifkkgveeFyakakeagvdgvlvaDlPleeaddlleaakk 138
                                               ++++ +e+++++r++ s+ P+vl+ y n++ + g+e+F ++a++ag+dgvl +D+P eead++    k+
  lcl|NCBI__GCF_002151265.1:WP_086508781.1  77 RLTHLFEMVREFRQRDSDTPVVLMGYLNPVERIGLEAFADQAAAAGIDGVLTVDMPPEEADEFGPILKQ 145
                                               ********************************************************************* PP

                                 TIGR00262 139 hgvkqiflvaPtaeeerlkkiaekseGfvYlvsvaGvtgarerveeevkelikkvkalskkPvlvGFGi 207
                                               +g++ iflvaPt+++er  +i  ++eG+ Y v+  Gvtga +  +++v e ++ ++ l++ P +vGFGi
  lcl|NCBI__GCF_002151265.1:WP_086508781.1 146 RGLASIFLVAPTTSSERAATICAHGEGYLYYVALKGVTGAATLNAADVAEHLAPLRGLTELPLCVGFGI 214
                                               ********************************************************************* PP

                                 TIGR00262 208 skkeqvkelkelgadgvivGsAlvkiieeklddeekaleeleefvkelk 256
                                                    + e+ ++ adgvivGsAlv +i+++ + +e++ +el+++  e++
  lcl|NCBI__GCF_002151265.1:WP_086508781.1 215 RDGASAAEVGKV-ADGVIVGSALVSRIADNAERPEAIADELKAVLGEMR 262
                                               *********999.9****************************9999885 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (256 nodes)
Target sequences:                          1  (271 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: 9.50
//
[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