GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Acidovorax sp. GW101-3H11

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate Ac3H11_214 Ferredoxin reductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_214
          Length = 431

 Score =  292 bits (747), Expect = 1e-83
 Identities = 174/403 (43%), Positives = 227/403 (56%), Gaps = 8/403 (1%)

Query: 2   SADPFVIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRA 61
           SA   VIVGAG A    A+ALR+      +V+IG E   P++RP LSK  L      +  
Sbjct: 22  SAHTIVIVGAGQAGGWAAQALRSEGFAGRVVLIGDEAHPPHERPPLSKAVLSGAAAPEST 81

Query: 62  FVRDAAWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPID 121
            +     +DA  +  R G +V  I+R A++V L DGT  PY KL+L TG R R    P  
Sbjct: 82  RLMKPEAFDALAVQWRPGMQVHRIDRAAKQVLLSDGTAQPYDKLILCTGGRARRLAVPGA 141

Query: 122 AGVVAHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLL 181
             V  H +RT+ DA+AL   L  GR V V+GGG+IGLEVAA ARQ G  V V++  +RL 
Sbjct: 142 DQVPLHTLRTIEDAQALAPALRPGRSVVVVGGGWIGLEVAATARQQGAEVVVVETQSRLC 201

Query: 182 QRALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGG-------GAIVETDRGDVHADV 234
           +R++P  V AY   LH  +GV   +    R    AA G         ++  D   +  D 
Sbjct: 202 ERSVPAEVSAYLLALHRAQGVRVLLGAGVRGFARAADGADGADSRSEVLLADGSALACDT 261

Query: 235 VVVGIGVLPNVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIES 294
           +V+G+G++PN ELA+AAGL  D G+RVDA CRT+D  I AAG+V +  NP +GR +R+ES
Sbjct: 262 IVLGVGLVPNDELARAAGLACDGGVRVDAQCRTSDPHILAAGDVAVAPNPWVGRSLRLES 321

Query: 295 WQVAENQPAVAAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAGQTTVVRGDPARGPF 354
           WQ A+ Q   AA + LG    Y  LPW WSDQY  NLQ+ G+       V RGDPA G F
Sbjct: 322 WQNAQEQGMAAARSALGQAVDYQPLPWFWSDQYGTNLQIYGMPTPAHLVVPRGDPASGSF 381

Query: 355 TVFGLGGDGRIVAAAAVNLGRDIGAARRLIAAGAMPDPQQLAD 397
            +F L GD  + AA   N  RD+  ARRLI      D ++LAD
Sbjct: 382 VLFYLAGD-VVQAAVGANAARDLRFARRLIDQRKPVDAERLAD 423


Lambda     K      H
   0.322    0.138    0.410 

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: 406
Number of extensions: 19
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: 406
Length of database: 431
Length adjustment: 32
Effective length of query: 374
Effective length of database: 399
Effective search space:   149226
Effective search space used:   149226
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: 50 (23.9 bits)

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:

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