GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruF in Sphingomonas koreensis DSMZ 15582

Align arginine N-succinyltransferase; EC 2.3.1.109 (characterized)
to candidate Ga0059261_3996 Ga0059261_3996 arginine and ornithine succinyltransferase subunits

Query= CharProtDB::CH_107315
         (338 letters)



>FitnessBrowser__Korea:Ga0059261_3996
          Length = 336

 Score =  185 bits (470), Expect = 1e-51
 Identities = 113/332 (34%), Positives = 173/332 (52%), Gaps = 3/332 (0%)

Query: 3   VMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYFFV 62
           ++RPA+  DL  +  +A  +  G T+LP +   LR K+  S  +F+       +E +  V
Sbjct: 4   LIRPAREDDLQALYEMAKLTGGGFTNLPPEKPALRAKLERSALAFSRTDDALKDELFVLV 63

Query: 63  LEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGNSL 122
           LE+S + E+ G   I    G   PFYS+R       S +L+   +  +LSL +DL G S 
Sbjct: 64  LENSETHEVRGTCQIFTQVGQRWPFYSYRLGIETKHSEALARTFRAEILSLTNDLEGCSE 123

Query: 123 LTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAVGR 182
           +   ++           L +R R LF+A H  RF D V+ E+ G  DE G SPFW+ V  
Sbjct: 124 VGGLFLHPGERAGGLGMLLARSRYLFIAMHRARFGDRVLAELRGVIDEAGGSPFWDGVAG 183

Query: 183 NFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDILMR 242
            FF +N+ +A++ + +    F+A+LMP +PIY  +L + A+  +G  HP  +    +L +
Sbjct: 184 RFFGMNFQQADEFNAIHGNQFIADLMPKHPIYTAMLTEGARSVIGLPHPSGRAAMRMLEQ 243

Query: 243 EGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAPKSGRPYLVTNGQLQDFRA 302
           EGF  +NYIDIFDGGPT+ ART  + ++  SR    K+ +    G   ++  G L DFRA
Sbjct: 244 EGFAFENYIDIFDGGPTMTARTDQVMTVRDSRT--DKVVDIADGGSASIIARGTLSDFRA 301

Query: 303 VVLDLDWAPGKPVALSVEAAEALGVGEGASVR 334
               +  + G  V +   +A  LGV  G  VR
Sbjct: 302 CHGRIGLSDG-GVTVDAMSASILGVEAGQEVR 332


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: 244
Number of extensions: 12
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: 336
Length adjustment: 28
Effective length of query: 310
Effective length of database: 308
Effective search space:    95480
Effective search space used:    95480
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