GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Sinorhizobium meliloti 1021

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate SMc02016 SMc02016 ferredoxin reductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__Smeli:SMc02016
          Length = 420

 Score =  224 bits (571), Expect = 4e-63
 Identities = 143/405 (35%), Positives = 209/405 (51%), Gaps = 12/405 (2%)

Query: 7   VIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRAFVRDA 66
           VIVG GHA  R A+ALR       I ++  E   PY+RP LSK  L  +   + A +  A
Sbjct: 14  VIVGCGHAGARAAQALRTNGWHGGITLVDGEGRTPYERPPLSKAVLKGESEAEDAPLFPA 73

Query: 67  AWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPIDAGVVA 126
            +     I +  G    AI+R  +++RL DG ++ Y +L+LATG+  R    P      +
Sbjct: 74  DFLAKNDIHVLKGVAAAAIDRPTRQLRLSDGGSIAYHRLLLATGAEPRNLIVPGADLPGS 133

Query: 127 HYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLLQRALP 186
           H +R+  DA  +   L  G  + ++GGG IGLE AA+A   GC VTV++   R + RA+P
Sbjct: 134 HTLRSADDAARIFPYLRPGAEIVIVGGGLIGLEAAASATVRGCKVTVVEAGPRPMMRAVP 193

Query: 187 EVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAI--VETDRGDV-HADVVVVGIGVLP 243
             +       H+ + V F    L R +    G G +  V  D G V     VV+ +GV P
Sbjct: 194 AELSHEVRLFHESKDVRF---VLGRQVSELEGDGRVRCVRLDDGTVLPCTAVVISVGVSP 250

Query: 244 NVELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIESWQVAENQPA 303
              LA+AAGL++DNGI VD   RT+D  I+AAG+    F  + G  +R+E W+ AE+Q  
Sbjct: 251 RTALAEAAGLEIDNGIAVDRFLRTSDPFIYAAGDACA-FEQVSGPRMRLECWKNAEDQGT 309

Query: 304 VAAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAGQTTVVRGDPARGPFTVFGLGGDG 363
           +A  N+LG+D+AY  LPW+WSDQ+D  +Q+ G  G     V R  P      ++ L  D 
Sbjct: 310 LAGRNMLGSDEAYVPLPWMWSDQFDRTMQIAGQAGGSAEDVRRRCP-DSTLLIYHLDKDQ 368

Query: 364 RIVAAAAVNLGRDIGAARR----LIAAGAMPDPQQLADPTVGLKT 404
            I+  +     R++    R    L+  G  P  + LADP   L++
Sbjct: 369 MILGISGFGSIREVSRGVRMGQLLMERGIRPGRKALADPEFDLRS 413


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: 385
Number of extensions: 23
Number of successful extensions: 5
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: 420
Length adjustment: 31
Effective length of query: 375
Effective length of database: 389
Effective search space:   145875
Effective search space used:   145875
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