GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruF in Burkholderia phytofirmans PsJN

Align arginine N-succinyltransferase; EC 2.3.1.109 (characterized)
to candidate BPHYT_RS07700 BPHYT_RS07700 arginine N-succinyltransferase

Query= CharProtDB::CH_107315
         (338 letters)



>FitnessBrowser__BFirm:BPHYT_RS07700
          Length = 352

 Score =  287 bits (734), Expect = 3e-82
 Identities = 155/339 (45%), Positives = 214/339 (63%), Gaps = 5/339 (1%)

Query: 1   MLVMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYF 60
           ML +RP + ADL  ++ +A  +   + SLP D   L  ++  SE SF AEV + GEE Y 
Sbjct: 1   MLFVRPGRLADLDALEHMARTAQPVLHSLPHDRRALEARVALSEDSFRAEVDFPGEEFYL 60

Query: 61  FVLEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGN 120
           FVLEDS SG+L+G ++IVA+AG+S+PFY+FRN+  +HASR L ++ KIH L++ H+LTG 
Sbjct: 61  FVLEDSESGKLMGTASIVAAAGYSDPFYAFRNDALIHASRELHVNRKIHALTMSHELTGK 120

Query: 121 SLLTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAV 180
           S L  +Y+   L     A L SR R++++A++ +RF   V   ++G +DE G SPFW AV
Sbjct: 121 SRLAGYYIDPSLRGDAAAHLMSRARMMYIAANRKRFTPEVFSLLLGVTDENGVSPFWEAV 180

Query: 181 GRNFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDIL 240
           GR FF  N+ + E  SG +SRTF+AE+MP YPIYVPLLP+AAQ  +G+   +A + +DI 
Sbjct: 181 GRKFFGRNFADIEIESGGRSRTFIAEVMPTYPIYVPLLPEAAQRVLGEPDSKALLAYDIH 240

Query: 241 MREGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAPKSGRPYLVT-NGQLQD 299
           + EGFETD YIDIFD GP L A+      + ++    V    A   G  YL+  NG   +
Sbjct: 241 LEEGFETDRYIDIFDAGPVLTAQVDRSACVTRNETRVVHENNASADGSTYLIAHNGADGE 300

Query: 300 FRAVVLDLDWAPGKPVALSV--EAAEALGVGEGASVRLV 336
           FR V+ +L  A GK    S+   A  ALGV EG +VR V
Sbjct: 301 FRCVLGEL--AAGKEAGASLPHAAGAALGVEEGDTVRCV 337


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: 344
Number of extensions: 10
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: 338
Length of database: 352
Length adjustment: 29
Effective length of query: 309
Effective length of database: 323
Effective search space:    99807
Effective search space used:    99807
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