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 SMc00914 SMc00914 oxidoreductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__Smeli:SMc00914
          Length = 405

 Score =  243 bits (621), Expect = 6e-69
 Identities = 161/403 (39%), Positives = 209/403 (51%), Gaps = 7/403 (1%)

Query: 7   VIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRAFVRDA 66
           V+VG G AA      LRA     PI ++ AE  LPY RP LSK  LL +    R   R  
Sbjct: 6   VVVGGGQAAFALVAKLRALKDMRPITVVAAEASLPYQRPPLSKKYLLREMTLDRLLYRPE 65

Query: 67  AWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGGPIDAGVVA 126
           AWY    I +RL T V  ++R A++V L DG+ L Y  L  ATG+  R     +   +  
Sbjct: 66  AWYAEHEIDIRLSTTVTRVDRLAKQVALSDGSMLTYETLAFATGATPRRLPAAVGGDLAG 125

Query: 127 HY-VRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLLQRAL 185
            + VR   DA  L  ++  GRRV V+GGG+IGLE AA AR  G  VTVI+ A R+LQR  
Sbjct: 126 VFVVRDFRDADRLAEEMQPGRRVLVVGGGYIGLEAAAVARTSGLEVTVIEMADRILQRVA 185

Query: 186 PEVVGAYAHRLHDERGVGFQMAT-LPRAIRAAAGGGAIVETDRGDVHADVVVVGIGVLPN 244
                A    +H   GV  +  T L R I       A   +D   +  D+V+VGIGV  N
Sbjct: 186 SAATSAIVREIHRSHGVDIRERTGLHRLIGDNGRVTAAELSDGSVIPVDIVIVGIGVAAN 245

Query: 245 VELAQAAGLDVDNGIRVDAGCRTADRAIFAAGEVTMHFNPLLGRHVRIESWQVAENQPAV 304
             LA  AG++  NGI VD+  RT+D  I A G+  +   P  G  +R+ES Q A +Q   
Sbjct: 246 DALAHEAGIETANGIVVDSHGRTSDPTIVAMGDCAV--LPWDGMRIRLESVQNAVDQAEA 303

Query: 305 AAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAG-QTTVVRGDPARGPFTVFGLGGDG 363
            AA L G  D Y   PW WSDQYD  LQ+ G FG G   T+VR    +G  +V+     G
Sbjct: 304 VAAVLAGGTDPYDPKPWFWSDQYDVKLQIAG-FGLGHDETLVRQGQRQGSVSVWYF-RQG 361

Query: 364 RIVAAAAVNLGRDIGAARRLIAAGAMPDPQQLADPTVGLKTFL 406
           +++A  A+N  +     ++L+ AGA PD   LADP V LK  L
Sbjct: 362 KLIAVDAINDAKAYVTGKKLLEAGATPDRLLLADPQVDLKALL 404


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: 379
Number of extensions: 19
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: 405
Length adjustment: 31
Effective length of query: 375
Effective length of database: 374
Effective search space:   140250
Effective search space used:   140250
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