GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruF in Caulobacter crescentus NA1000

Align arginine N-succinyltransferase; EC 2.3.1.109 (characterized)
to candidate CCNA_01678 CCNA_01678 arginine N-succinyltransferase, beta chain

Query= CharProtDB::CH_107315
         (338 letters)



>FitnessBrowser__Caulo:CCNA_01678
          Length = 334

 Score =  201 bits (512), Expect = 2e-56
 Identities = 120/337 (35%), Positives = 185/337 (54%), Gaps = 3/337 (0%)

Query: 1   MLVMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYF 60
           MLV+RPA +AD   +  LA  S  G TSLP+D   LR ++  SEASF A V+   E  Y 
Sbjct: 1   MLVVRPAGSADFEALMELAVLSGRGFTSLPEDEPTLRSRLALSEASFQAGVA-PPEAWYT 59

Query: 61  FVLEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGN 120
            +LED  +G + G + + A  G   PF+SFR  T   +S +L +      L L ++  G 
Sbjct: 60  LMLEDLETGTVEGVAGVKAGVGLKRPFFSFRVVTLAQSSPTLEMRFDHKALVLVNECAGW 119

Query: 121 SLLTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAV 180
           S + S +++ +  +     L ++ R + +   P+RFA+ V+ E+ G+ DE G  PFW  V
Sbjct: 120 SEVGSLFLRPEKRKGGAGRLLAQSRYMLIGIEPQRFAEMVLAELRGWFDEDGRCPFWEHV 179

Query: 181 GRNFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDIL 240
              FF L++ +A+ +S      F+ +L P +PIY  LLP+ A++ +G+VH   +    +L
Sbjct: 180 SHKFFRLDFDQADLMSASTDGQFILDLAPRHPIYTELLPEEARDVIGRVHRDGEAARAML 239

Query: 241 MREGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAPKSGRPYLVTNGQLQDF 300
            REGF     +D+FD GPT+      IR++  +R + VK+GE    G   L++ G++  F
Sbjct: 240 EREGFRYQGLVDLFDAGPTVACPRDDIRTVRDARRLRVKVGE-DAYGEEALISTGEVSRF 298

Query: 301 RAVVLDLDWAPGKPVALSVEAAEALGVGEGASVRLVA 337
           RAV   +    G+   L  +A +ALGVGEG  VR+ A
Sbjct: 299 RAVRAPV-LIDGETAILGRDAMDALGVGEGEVVRVKA 334


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: 265
Number of extensions: 11
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: 334
Length adjustment: 28
Effective length of query: 310
Effective length of database: 306
Effective search space:    94860
Effective search space used:    94860
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