GapMind for Amino acid biosynthesis

 

Alignments for a candidate for trpA in Stenotrophomonas chelatiphaga DSM 21508

Align Tryptophan synthase alpha chain; EC 4.2.1.20 (characterized, see rationale)
to candidate WP_057687221.1 ABB28_RS15195 tryptophan synthase subunit alpha

Query= uniprot:M4NLA4
         (266 letters)



>NCBI__GCF_001431535.1:WP_057687221.1
          Length = 269

 Score =  300 bits (769), Expect = 2e-86
 Identities = 164/267 (61%), Positives = 194/267 (72%), Gaps = 2/267 (0%)

Query: 1   MSRIDRRFAALKAANRTGLIPFVTAGDPSPEHMVALMHALVDAGADLIELGVPFSDPMAD 60
           +SR+D RF  L+ A R  LIPF+TAGDPS E  V +MHALV+AGAD++ELGVPFSDPMAD
Sbjct: 3   VSRLDARFQRLRDAQRKALIPFITAGDPSLEATVPVMHALVEAGADVLELGVPFSDPMAD 62

Query: 61  GPVIQHASERAIAKGVGLADVLGWVAAFRQHDADTPIVLMGYLNPIETHGYARFAGEAVQ 120
           GP IQ +SERA+A+G GL  VL  VA FR  D+DTP+VLMGYLNP+E HGYARFA EAV 
Sbjct: 63  GPTIQRSSERALARGAGLRYVLQAVAEFRSRDSDTPVVLMGYLNPVEIHGYARFATEAVA 122

Query: 121 AGVDGVLLVDCPLEESAVLQPLRD-AGLQRILLAAPTTEPSRMAQLCGSAEGFLYYVSFA 179
           AGVDG+LLVD P EE+       D AGL  +LLA+PTT  +R   L G A G+LYYVSFA
Sbjct: 123 AGVDGILLVDLPPEEAHEANEAFDAAGLALVLLASPTTSDARADTLLGLARGYLYYVSFA 182

Query: 180 GITGAAHLSTGDIA-ARVADVRARAKAPVAVGFGIRDAASAKAIAGFADAVVIGSALVDR 238
           G+TGA+ L   D A AR+  +RARA  PV  GFGI+DA SA A+A  AD VV+GSALV  
Sbjct: 183 GVTGASDLLDHDAAGARLQALRARASVPVVAGFGIKDAGSAAAMARQADGVVVGSALVSV 242

Query: 239 LAGATDAGEITRRTQAFLAPIRAALDA 265
           LA AT   +  +   AFLAP+R ALDA
Sbjct: 243 LAQATTVEDAVQAAGAFLAPLRQALDA 269


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: 280
Number of extensions: 12
Number of successful extensions: 3
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: 269
Length adjustment: 25
Effective length of query: 241
Effective length of database: 244
Effective search space:    58804
Effective search space used:    58804
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_057687221.1 ABB28_RS15195 (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.17382.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
    2.5e-73  232.1   0.0    2.8e-73  231.9   0.0    1.0  1  lcl|NCBI__GCF_001431535.1:WP_057687221.1  ABB28_RS15195 tryptophan synthas


Domain annotation for each sequence (and alignments):
>> lcl|NCBI__GCF_001431535.1:WP_057687221.1  ABB28_RS15195 tryptophan synthase subunit alpha
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  231.9   0.0   2.8e-73   2.8e-73       1     252 [.      10     260 ..      10     264 .. 0.95

  Alignments for each domain:
  == domain 1  score: 231.9 bits;  conditional E-value: 2.8e-73
                                 TIGR00262   1 fetlkkkeekafvpFvtagdPdleksleiiktlvkaGadalElGvpfsDPlaDGptiqaaelRAlkagv 69 
                                               f+ l++++ ka++pF+tagdP+le ++ +++ lv+aGad+lElGvpfsDP+aDGptiq+++ RAl++g 
  lcl|NCBI__GCF_001431535.1:WP_057687221.1  10 FQRLRDAQRKALIPFITAGDPSLEATVPVMHALVEAGADVLELGVPFSDPMADGPTIQRSSERALARGA 78 
                                               78899**************************************************************** PP

                                 TIGR00262  70 kvekalellkkvrekasniPivlltyynlifkkgveeFyakakeagvdgvlvaDlPleeaddlleaakk 138
                                                ++ +l+ ++++r++ s+ P+vl+ y n++  +g   F ++a +agvdg+l++DlP eea+++ ea   
  lcl|NCBI__GCF_001431535.1:WP_057687221.1  79 GLRYVLQAVAEFRSRDSDTPVVLMGYLNPVEIHGYARFATEAVAAGVDGILLVDLPPEEAHEANEAFDA 147
                                               ********************************************************************* PP

                                 TIGR00262 139 hgvkqiflvaPtaeeerlkkiaekseGfvYlvsvaGvtgarerveee.vkelikkvkalskkPvlvGFG 206
                                                g++ ++l++Pt+++ r  ++   ++G+ Y vs aGvtga++ ++++ + + ++ ++a +++Pv+ GFG
  lcl|NCBI__GCF_001431535.1:WP_057687221.1 148 AGLALVLLASPTTSDARADTLLGLARGYLYYVSFAGVTGASDLLDHDaAGARLQALRARASVPVVAGFG 216
                                               ********************************************88746789***************** PP

                                 TIGR00262 207 iskkeqvkelkelgadgvivGsAlvkiieeklddeekaleeleefv 252
                                               i  +  + ++    adgv+vGsAlv ++++   + e a+++  +f 
  lcl|NCBI__GCF_001431535.1:WP_057687221.1 217 IKDAGSAAAMARQ-ADGVVVGSALVSVLAQA-TTVEDAVQAAGAFL 260
                                               ****999988887.9*************999.56777777766665 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (256 nodes)
Target sequences:                          1  (269 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: 7.34
//
[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