Alignments for a candidate for tpi in Pseudomonas stutzeri RCH2

GapMind for catabolism of small carbon sources

Alignments for a candidate for tpi in Pseudomonas stutzeri RCH2

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate GFF946 Psest_0975 triosephosphate isomerase

Query= BRENDA::P0A858
         (255 letters)



>FitnessBrowser__psRCH2:GFF946
          Length = 251

 Score =  235 bits (600), Expect = 6e-67
 Identities = 123/250 (49%), Positives = 165/250 (66%), Gaps = 2/250 (0%)

Query: 1   MRHPLVMGNWKLNGSRHMVHELVSNLRKELAGVAGCAVAIAPPEMYIDMAKREAEGSHIM 60
           MR P+V GNWK+NG+R  V ELV +LR +   V+   +A+ P  +++       +  H+ 
Sbjct: 1   MRRPMVAGNWKMNGTRASVAELVESLRMQALPVS-VEIAVFPSCLHVAQVLGGVDSKHVA 59

Query: 61  LGAQNVDL-NLSGAFTGETSAAMLKDIGAQYIIIGHSERRTYHKESDELIAKKFAVLKEQ 119
           +GAQ+    N  GA TGE SA    ++G +++++GHSERR    E+DE++++KF   +  
Sbjct: 60  VGAQDCAAQNGFGALTGEVSAEQFAEVGCEWVLVGHSERRLVLGETDEVVSRKFLAAQVG 119

Query: 120 GLTPVLCIGETEAENEAGKTEEVCARQIDAVLKTQGAAAFEGAVIAYEPVWAIGTGKSAT 179
           GL PVLC+GET  E EAG+T EV  RQ+  VL   G A FE AVIAYEPVWAIG+G +AT
Sbjct: 120 GLKPVLCLGETLEEREAGRTLEVVGRQLAQVLDDHGIAVFESAVIAYEPVWAIGSGLTAT 179

Query: 180 PAQAQAVHKFIRDHIAKVDANIAEQVIIQYGGSVNASNAAELFAQPDIDGALVGGASLKA 239
           P QAQ VH  IR+ +++ D  +A  V + YGGSV A NAAELF+  DIDG LVGGASLKA
Sbjct: 180 PEQAQEVHAAIREQLSRQDRQVAAGVRLLYGGSVKADNAAELFSMADIDGGLVGGASLKA 239

Query: 240 DAFAVIVKAA 249
           + F  I +AA
Sbjct: 240 NEFGAICRAA 249


Lambda     K      H
   0.316    0.130    0.366 

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: 180
Number of extensions: 8
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: 251
Length adjustment: 24
Effective length of query: 231
Effective length of database: 227
Effective search space:    52437
Effective search space used:    52437
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: 41 (21.6 bits)
S2: 46 (22.3 bits)

Align candidate GFF946 Psest_0975 (triosephosphate isomerase)
to HMM TIGR00419 (tpiA: triose-phosphate isomerase (EC 5.3.1.1))

# 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.carbon/TIGR00419.hmm
# target sequence database:        /tmp/gapView.27483.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       TIGR00419  [M=228]
Accession:   TIGR00419
Description: tim: triose-phosphate isomerase
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-68  216.6   2.3    2.4e-68  216.4   2.3    1.0  1  lcl|FitnessBrowser__psRCH2:GFF946  Psest_0975 triosephosphate isome


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__psRCH2:GFF946  Psest_0975 triosephosphate isomerase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  216.4   2.3   2.4e-68   2.4e-68       1     228 []       5     240 ..       5     240 .. 0.92

  Alignments for each domain:
  == domain 1  score: 216.4 bits;  conditional E-value: 2.4e-68
                          TIGR00419   1 lviinfKlnesvgkvelevaklaeevaseagvevavappfvdldvvkdeve.seiqvaAqnvdavk.sGaftGeis 74 
                                        +v +n+K+n+++ +v+++v +l+ + a +  ve+av p+ +++  v   v+  ++ v+Aq++ a++ +Ga tGe+s
  lcl|FitnessBrowser__psRCH2:GFF946   5 MVAGNWKMNGTRASVAELVESLRMQ-ALPVSVEIAVFPSCLHVAQVLGGVDsKHVAVGAQDCAAQNgFGALTGEVS 79 
                                        699********************98.778899******************9789********986537******** PP

                          TIGR00419  75 AemlkdlGakgvligHsErRsllkeadeliekkvarlkelglksvvCvgetleereaartinnvattaaaaA.... 146
                                        Ae  +++G+++vl+gHsErR +l e+de++  k+  ++  glk+v+C+getleerea+rt+++v ++ a +     
  lcl|FitnessBrowser__psRCH2:GFF946  80 AEQFAEVGCEWVLVGHSERRLVLGETDEVVSRKFLAAQVGGLKPVLCLGETLEEREAGRTLEVVGRQLAQVLddhg 155
                                        ********************************************************66666666555443333333 PP

                          TIGR00419 147 ...lepdvvAvEPveliGtGkpvskAeaevveksvrdhlkkvskevaesvrvlyGasvtaaedaelaaqldvdGvL 219
                                           +e++v+A+EPv++iG+G ++++ +a++v++ +r+ l++ +++va  vr+lyG+sv+a ++ael+   d+dG L
  lcl|FitnessBrowser__psRCH2:GFF946 156 iavFESAVIAYEPVWAIGSGLTATPEQAQEVHAAIREQLSRQDRQVAAGVRLLYGGSVKADNAAELFSMADIDGGL 231
                                        334************************************************************************* PP

                          TIGR00419 220 lasavlkae 228
                                        +++a+lka+
  lcl|FitnessBrowser__psRCH2:GFF946 232 VGGASLKAN 240
                                        *******95 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (228 nodes)
Target sequences:                          1  (251 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: 5.88
//
[ok]

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources