Aligments for a candidate for nbaC in Dyella japonica UNC79MFTsu3.2

GapMind for catabolism of small carbon sources

Aligments for a candidate for nbaC in Dyella japonica UNC79MFTsu3.2

Align 3-hydroxyanthranilate 3,4-dioxygenase; 3-hydroxyanthranilate oxygenase; 3-HAO; 3-hydroxyanthranilic acid dioxygenase; HAD; EC 1.13.11.6 (characterized)
to candidate N515DRAFT_2922 N515DRAFT_2922 3-hydroxyanthranilate 3,4-dioxygenase

Query= SwissProt::Q1LCS4
         (174 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2922
          Length = 173

 Score =  171 bits (433), Expect = 6e-48
 Identities = 87/167 (52%), Positives = 101/167 (60%), Gaps = 2/167 (1%)

Query: 7   PFNFPRWIDEHAHLLKPPVGNRQVWQDSDFIVTVVGGPNHRTDYHDDPLEEFFYQLRGNA 66
           P +  RWIDEH HLLKPPVGN+ +  D DFIV +VGGPN RTDYH D   EFFYQL G  
Sbjct: 6   PLDLQRWIDEHRHLLKPPVGNKCI-VDGDFIVMIVGGPNARTDYHYDEGPEFFYQLEGEM 64

Query: 67  YLNLWVDGRRERADLKEGDIFLLPPHVRHSPQRPEAGSACLVIERQRPAGMLDGFEWYCD 126
            L +  DG      ++ G +F LPP V HSPQR    S  LVIER+R AG  DG  W+C 
Sbjct: 65  VLKVQDDGAARDIPIRAGQMFYLPPRVPHSPQR-MPDSIGLVIERRRLAGEQDGLMWFCQ 123

Query: 127 ACGHLVHRVEVQLKSIVTDLPPLFESFYASEDKRRCPHCGQVHPGRA 173
            C H ++     L SI  D PP+FE FY S + R C  CG VHP  A
Sbjct: 124 QCNHKLYEEYFTLDSIERDFPPVFERFYRSLEARTCTQCGTVHPAPA 170


Lambda     K      H
   0.324    0.143    0.481 

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: 159
Number of extensions: 6
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: 174
Length of database: 173
Length adjustment: 19
Effective length of query: 155
Effective length of database: 154
Effective search space:    23870
Effective search space used:    23870
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 bits)
S2: 44 (21.6 bits)

Align candidate N515DRAFT_2922 N515DRAFT_2922 (3-hydroxyanthranilate 3,4-dioxygenase)
to HMM TIGR03037 (nbaC: 3-hydroxyanthranilate 3,4-dioxygenase (EC 1.13.11.6))

# 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/TIGR03037.hmm
# target sequence database:        /tmp/gapView.30844.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       TIGR03037  [M=159]
Accession:   TIGR03037
Description: anthran_nbaC: 3-hydroxyanthranilate 3,4-dioxygenase
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-81  256.3   0.0    6.3e-81  256.1   0.0    1.0  1  lcl|FitnessBrowser__Dyella79:N515DRAFT_2922  N515DRAFT_2922 3-hydroxyanthrani


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__Dyella79:N515DRAFT_2922  N515DRAFT_2922 3-hydroxyanthranilate 3,4-dioxygenase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  256.1   0.0   6.3e-81   6.3e-81       1     159 []       7     164 ..       7     164 .. 0.99

  Alignments for each domain:
  == domain 1  score: 256.1 bits;  conditional E-value: 6.3e-81
                                    TIGR03037   1 lnlkkwidehkellkppvgnkqiwqdselivtvvGGpnkrtdfhvdeseeffyqlkGemvlkvlee 66 
                                                  l+l++wideh++llkppvgnk+i  d ++iv++vGGpn+rtd+h+de++effyql+Gemvlkv+++
  lcl|FitnessBrowser__Dyella79:N515DRAFT_2922   7 LDLQRWIDEHRHLLKPPVGNKCI-VDGDFIVMIVGGPNARTDYHYDEGPEFFYQLEGEMVLKVQDD 71 
                                                  579********************.899*************************************** PP

                                    TIGR03037  67 GkvedvpireGdifllppkvphspqraagsiglvierkrkegeldalqwfcaecgeklyraevkle 132
                                                  G ++d+pir+G++f lpp+vphspqr  +siglvier+r  ge+d+l+wfc++c++kly++ ++l+
  lcl|FitnessBrowser__Dyella79:N515DRAFT_2922  72 GAARDIPIRAGQMFYLPPRVPHSPQRMPDSIGLVIERRRLAGEQDGLMWFCQQCNHKLYEEYFTLD 137
                                                  ****************************************************************** PP

                                    TIGR03037 133 sivkdlppvfekfyssedartckkcGe 159
                                                  si++d+ppvfe+fy+s +artc++cG+
  lcl|FitnessBrowser__Dyella79:N515DRAFT_2922 138 SIERDFPPVFERFYRSLEARTCTQCGT 164
                                                  *************************96 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (159 nodes)
Target sequences:                          1  (173 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: 5.92
//
[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, or view the source code.

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