GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Burkholderia phytofirmans PsJN

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate BPHYT_RS21090 BPHYT_RS21090 FAD-dependent pyridine nucleotide-disulfide oxidoreductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__BFirm:BPHYT_RS21090
          Length = 409

 Score =  179 bits (455), Expect = 1e-49
 Identities = 130/388 (33%), Positives = 192/388 (49%), Gaps = 21/388 (5%)

Query: 8   IVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRAFVRDAA 67
           IVG G AA R  E LR    D  I ++ AE  LPYDRP LSKD LL          RD A
Sbjct: 14  IVGGGLAALRCTEELRRGGHDGRIAIVTAEPHLPYDRPPLSKDVLLGAKEFDEVQYRDDA 73

Query: 68  WYDAQRIALRLG---TRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPIDAGV 124
           +Y   ++ + L    T +  +ERE     + +G+ + +  L++ TG+  R+F  P+ +  
Sbjct: 74  FYRDHQVDMYLSHPATELRILEREV----VANGSAIAFDDLLICTGASPRSF--PLKSNC 127

Query: 125 VAHY-VRTVADARALRAQLVRGR-RVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLLQ 182
              Y +  + D   LRA L  G  RV +LG GFIG EVA+ AR LG   T+++ AA  L+
Sbjct: 128 DGIYTLGRIEDTLRLRAALRSGAPRVVILGAGFIGAEVASCARSLGLETTIVNLAATPLE 187

Query: 183 RALPEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVE---TDRGDVHADVVVVGI 239
           RA+   +G     LH + GV    +    +I    G G + E   T+   +  D++V+GI
Sbjct: 188 RAVGPEMGGMLSALHADHGVRLLCSV---SIAEIFGDGRVEELLLTNGERIACDILVIGI 244

Query: 240 GVLPNVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIESWQVAE 299
           G  PN+   + +GL++ NGI  DA        I+AAG+V    N L GR +R E W  A 
Sbjct: 245 GSTPNIGWLEGSGLELANGIVCDAALSAGPPGIYAAGDVAWWPNGLFGRGMRCEQWTNAA 304

Query: 300 NQPAVAAANLLGADDA---YAELPWLWSDQYDCNLQMLGLFGAGQTTVVRGDPARGPFTV 356
            Q    A N+L   +    +    + WSDQY   +Q  G   A +  +V+G    G F  
Sbjct: 305 EQGRHVARNILAGHEGRTPFVGSNYFWSDQYGKRIQFAGSEVADEVKIVKGSYGEGHFLA 364

Query: 357 FGLGGDGRIVAAAAVNLGRDIGAARRLI 384
           +   GD ++  A A+N  + +  A++ I
Sbjct: 365 YYRKGD-QLCGALALNEPKSLMLAKQQI 391


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: 322
Number of extensions: 17
Number of successful extensions: 4
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: 409
Length adjustment: 31
Effective length of query: 375
Effective length of database: 378
Effective search space:   141750
Effective search space used:   141750
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