GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruF in Marinobacter adhaerens HP15

Align arginine N-succinyltransferase; EC 2.3.1.109 (characterized)
to candidate GFF3097 HP15_3040 arginine N-succinyltransferase subunit beta

Query= CharProtDB::CH_107315
         (338 letters)



>FitnessBrowser__Marino:GFF3097
          Length = 366

 Score =  205 bits (522), Expect = 1e-57
 Identities = 118/340 (34%), Positives = 181/340 (53%), Gaps = 6/340 (1%)

Query: 1   MLVMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYF 60
           MLV+RP Q  DL  +  +A  +  G+T+LP D E L+ KI  +  +F   ++      Y 
Sbjct: 1   MLVIRPLQENDLDDLYAMAQSAGKGLTTLPADRELLQKKINHARETFNQRIAPEAG-LYL 59

Query: 61  FVLEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGN 120
           F LED+   + VG S I A  G  E FY++R    V+AS+ L +H +   L L +D+T  
Sbjct: 60  FALEDTERKKTVGISGIQARVGLDEVFYNYRLSVTVNASKELGVHVRTPTLHLSNDMTDT 119

Query: 121 SLLTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAV 180
           S + S  +  +        L SR R +++    + F++ +  E+ G SD  G SP W+A+
Sbjct: 120 SEICSLLLSDEYKGGGSGLLLSRCRFMYLDEFRKHFSEKIFAEMRGVSDANGRSPLWDAL 179

Query: 181 GRNFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDIL 240
           G  FFD+ + EA+ LSGL +++F+AELMP YPIY+ +LPD+A+  +G+VH        +L
Sbjct: 180 GTKFFDMEFSEADMLSGLGNKSFIAELMPKYPIYLSMLPDSARAVIGRVHDNTAPALRML 239

Query: 241 MREGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAP-----KSGRPYLVTNG 295
             EGF  +  +DIFDGGP + A    +R++ +       +   P      S    +V+N 
Sbjct: 240 QSEGFNFNGLVDIFDGGPVVEAFVHNVRTVREGMNRHAMVTRKPVNLDVPSEERVMVSNR 299

Query: 296 QLQDFRAVVLDLDWAPGKPVALSVEAAEALGVGEGASVRL 335
             +DFR   + +D      V+L  E AEAL +  G  VRL
Sbjct: 300 SFRDFRVTTVPIDCIGPDTVSLPPEVAEALQIESGDPVRL 339


Lambda     K      H
   0.319    0.135    0.387 

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: 284
Number of extensions: 9
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: 338
Length of database: 366
Length adjustment: 29
Effective length of query: 309
Effective length of database: 337
Effective search space:   104133
Effective search space used:   104133
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 (21.8 bits)
S2: 49 (23.5 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