GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruG 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= BRENDA::P80358
         (340 letters)



>FitnessBrowser__Caulo:CCNA_01678
          Length = 334

 Score =  223 bits (568), Expect = 5e-63
 Identities = 128/333 (38%), Positives = 192/333 (57%), Gaps = 6/333 (1%)

Query: 1   MIVRPVTSADLPALIELARSTGTGLTTLPANEQRLQHRVSWAEKAFRGEAERGDADYLFV 60
           ++VRP  SAD  AL+ELA  +G G T+LP +E  L+ R++ +E +F+      +A Y  +
Sbjct: 2   LVVRPAGSADFEALMELAVLSGRGFTSLPEDEPTLRSRLALSEASFQAGVAPPEAWYTLM 61

Query: 61  LED-DAGKVVGISAIAGAVGLREPWYNYRVGLTVSASQELNIHREIPTLFLANDLTGNSE 119
           LED + G V G++ +   VGL+ P++++RV     +S  L +  +   L L N+  G SE
Sbjct: 62  LEDLETGTVEGVAGVKAGVGLKRPFFSFRVVTLAQSSPTLEMRFDHKALVLVNECAGWSE 121

Query: 120 LCSLFLHADHRSGLNGKLLSRARFLFIAEFRHLFGDKLIAEMRGMSDEEGRSPFWESLGR 179
           + SLFL  + R G  G+LL+++R++ I      F + ++AE+RG  DE+GR PFWE +  
Sbjct: 122 VGSLFLRPEKRKGGAGRLLAQSRYMLIGIEPQRFAEMVLAELRGWFDEDGRCPFWEHVSH 181

Query: 180 HFFKMEFSQADYLTGVGNKAFIAELMPKFPLYTCFLSEEARGVIGRVHPNTEPALAMLKA 239
            FF+++F QAD ++   +  FI +L P+ P+YT  L EEAR VIGRVH + E A AML+ 
Sbjct: 182 KFFRLDFDQADLMSASTDGQFILDLAPRHPIYTELLPEEARDVIGRVHRDGEAARAMLER 241

Query: 240 EGFSYQGYVDIFDAGPAIEAETDKIRAIAESQNLVLAVGTPGDDA--EPYLIHNRKREDC 297
           EGF YQG VD+FDAGP +    D IR + +++ L + V   G+DA  E  LI   +    
Sbjct: 242 EGFRYQGLVDLFDAGPTVACPRDDIRTVRDARRLRVKV---GEDAYGEEALISTGEVSRF 298

Query: 298 RITAAPARAAAGTLVVDPLTAKRLRLSAGASVR 330
           R   AP      T ++       L +  G  VR
Sbjct: 299 RAVRAPVLIDGETAILGRDAMDALGVGEGEVVR 331


Lambda     K      H
   0.320    0.136    0.398 

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: 262
Number of extensions: 8
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: 340
Length of database: 334
Length adjustment: 28
Effective length of query: 312
Effective length of database: 306
Effective search space:    95472
Effective search space used:    95472
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