GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruF in Shewanella amazonensis SB2B

Align arginine N-succinyltransferase; EC 2.3.1.109 (characterized)
to candidate 6937471 Sama_1627 arginine N-succinyltransferase (RefSeq)

Query= CharProtDB::CH_107315
         (338 letters)



>FitnessBrowser__SB2B:6937471
          Length = 348

 Score =  234 bits (597), Expect = 2e-66
 Identities = 131/340 (38%), Positives = 193/340 (56%), Gaps = 7/340 (2%)

Query: 1   MLVMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYF 60
           ML++RP Q +D   +  +A +S  G TSLP    +L  KI  SE SFAA++   G++ Y 
Sbjct: 1   MLLIRPIQGSDFQALMTMARESGAGFTSLPLCERKLTHKIAHSEESFAADIDAPGDQGYL 60

Query: 61  FVLEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGN 120
           FVLED+ +GE++G S I AS G   P Y F   T VH  + L I N + VL+L +D TG 
Sbjct: 61  FVLEDTDTGEILGASGIEASVGLGSPLYHFHKSTVVHQCKELDIFNPVEVLTLGNDYTGV 120

Query: 121 SLLTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAV 180
           + + + +++      +     S+ R +FMA HP+RF+  V+ E+ G +DE G+ PFW  +
Sbjct: 121 TEICTLFLREPYRVGLNGRFLSKVRFMFMAEHPKRFSQLVIAEMRGAADENGQPPFWGWL 180

Query: 181 GRNFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDIL 240
              FF++ + +A+ L G+ ++ F+A+LMP YPIYV LLP+AA+ ++GQVH        +L
Sbjct: 181 RETFFNMEFSKADYLIGVGNKGFIADLMPRYPIYVDLLPEAARNTIGQVHENTVPALKLL 240

Query: 241 MREGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAP---KSGRPYLVTNGQL 297
             EGF    Y+D+FD GPT+ A+   I+S+ QS  V V I + P   K      V N   
Sbjct: 241 ENEGFMHRGYVDLFDAGPTVEAQLKQIKSVRQSHRVKVVISQNPAEHKGEFHLAVCNCDS 300

Query: 298 QDFRAVVLD---LDWAPGKPVALSVEAAEALGVGEGASVR 334
           + FRA V D   L+      + +S   A+ L V EG  VR
Sbjct: 301 KAFRATVSDECRLE-PETHSILMSPAMADVLNVAEGDLVR 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: 279
Number of extensions: 10
Number of successful extensions: 1
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: 348
Length adjustment: 29
Effective length of query: 309
Effective length of database: 319
Effective search space:    98571
Effective search space used:    98571
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.

Links

Downloads

Related tools

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