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_00617 CCNA_00617 arginine N-succinyltransferase, beta chain

Query= CharProtDB::CH_107315
         (338 letters)



>FitnessBrowser__Caulo:CCNA_00617
          Length = 347

 Score =  184 bits (466), Expect = 4e-51
 Identities = 111/331 (33%), Positives = 171/331 (51%), Gaps = 4/331 (1%)

Query: 3   VMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYFFV 62
           ++RPA+  DL  +  LA  +  G+T+LP D   L D++ ASE +     + N   + + V
Sbjct: 16  LVRPARRGDLDGLLALARAADAGMTNLPADRAALDDRLAASEQALIDPETRNAGAAVYLV 75

Query: 63  LEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGNSL 122
           LE    G ++G + + A  G ++PFYS+R       S  L    ++ VL+L +DLT  + 
Sbjct: 76  LE--RQGRVIGAACVFARIGVAQPFYSYRVTRLTQLSPDLGKRVEMSVLTLVNDLTDQAE 133

Query: 123 LTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAVGR 182
           +   +V  D  +     L +R R LFMA H + F + V+ ++ G  D  G SP W+A+G 
Sbjct: 134 VGGLFVAPDARKGQAGRLMARSRYLFMARHRDWFGEQVIADLRGVQDADGRSPVWDALGA 193

Query: 183 NFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDILMR 242
           +F+ +++  A++   L    F+++L P YPIYV LLP AAQ ++G+ H        +L  
Sbjct: 194 HFYAMDFAAADRACALSGTRFISDLGPKYPIYVGLLPPAAQAALGKPHQDGVGAERLLRE 253

Query: 243 EGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAPKSGRPYLVTNGQLQDFRA 302
           EGF +D Y+DIFDGGPTL AR   +++I ++R  P+  G         LV  G    FR 
Sbjct: 254 EGFVSDGYVDIFDGGPTLRARIDDLKAIREARRAPL-AGLTDTPTDDALVCAGAGAAFRV 312

Query: 303 VVLDLDWAPGKPVALSVEAAEALGVGEGASV 333
           V   L  A    V        ALG+  G  +
Sbjct: 313 VRGGLS-AGDDGVRAEASLINALGLAPGQEI 342


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: 239
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: 347
Length adjustment: 29
Effective length of query: 309
Effective length of database: 318
Effective search space:    98262
Effective search space used:    98262
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