GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruG in Marinobacter adhaerens HP15

Align arginine N-succinyltransferase (EC 2.3.1.109) (characterized)
to candidate GFF3097 HP15_3040 arginine N-succinyltransferase subunit beta

Query= BRENDA::P80358
         (340 letters)



>FitnessBrowser__Marino:GFF3097
          Length = 366

 Score =  300 bits (768), Expect = 4e-86
 Identities = 158/341 (46%), Positives = 215/341 (63%), Gaps = 7/341 (2%)

Query: 1   MIVRPVTSADLPALIELARSTGTGLTTLPANEQRLQHRVSWAEKAFRGEAERGDADYLFV 60
           +++RP+   DL  L  +A+S G GLTTLPA+ + LQ +++ A + F          YLF 
Sbjct: 2   LVIRPLQENDLDDLYAMAQSAGKGLTTLPADRELLQKKINHARETFNQRIAPEAGLYLFA 61

Query: 61  LED-DAGKVVGISAIAGAVGLREPWYNYRVGLTVSASQELNIHREIPTLFLANDLTGNSE 119
           LED +  K VGIS I   VGL E +YNYR+ +TV+AS+EL +H   PTL L+ND+T  SE
Sbjct: 62  LEDTERKKTVGISGIQARVGLDEVFYNYRLSVTVNASKELGVHVRTPTLHLSNDMTDTSE 121

Query: 120 LCSLFLHADHRSGLNGKLLSRARFLFIAEFRHLFGDKLIAEMRGMSDEEGRSPFWESLGR 179
           +CSL L  +++ G +G LLSR RF+++ EFR  F +K+ AEMRG+SD  GRSP W++LG 
Sbjct: 122 ICSLLLSDEYKGGGSGLLLSRCRFMYLDEFRKHFSEKIFAEMRGVSDANGRSPLWDALGT 181

Query: 180 HFFKMEFSQADYLTGVGNKAFIAELMPKFPLYTCFLSEEARGVIGRVHPNTEPALAMLKA 239
            FF MEFS+AD L+G+GNK+FIAELMPK+P+Y   L + AR VIGRVH NT PAL ML++
Sbjct: 182 KFFDMEFSEADMLSGLGNKSFIAELMPKYPIYLSMLPDSARAVIGRVHDNTAPALRMLQS 241

Query: 240 EGFSYQGYVDIFDAGPAIEAETDKIRAIAESQN-----LVLAVGTPGDDAEPYLIHNRKR 294
           EGF++ G VDIFD GP +EA    +R + E  N         V       E  ++ NR  
Sbjct: 242 EGFNFNGLVDIFDGGPVVEAFVHNVRTVREGMNRHAMVTRKPVNLDVPSEERVMVSNRSF 301

Query: 295 EDCRITAAPARA-AAGTLVVDPLTAKRLRLSAGASVRAVPL 334
            D R+T  P       T+ + P  A+ L++ +G  VR  PL
Sbjct: 302 RDFRVTTVPIDCIGPDTVSLPPEVAEALQIESGDPVRLAPL 342


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: 322
Number of extensions: 17
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: 366
Length adjustment: 29
Effective length of query: 311
Effective length of database: 337
Effective search space:   104807
Effective search space used:   104807
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