GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Burkholderia phytofirmans PsJN

Align asparaginase (EC 3.5.1.1) (characterized)
to candidate BPHYT_RS07040 BPHYT_RS07040 asparaginase

Query= BRENDA::Q9RFN5
         (371 letters)



>FitnessBrowser__BFirm:BPHYT_RS07040
          Length = 363

 Score =  444 bits (1143), Expect = e-129
 Identities = 217/341 (63%), Positives = 270/341 (79%), Gaps = 1/341 (0%)

Query: 16  RGGIVENSHRVHAAVVDAKGRLLYALGNPTRMTLARSAAKPAQALAILETEGVAGYGFDD 75
           RG  +EN+H  H AVVDA GRLL + G+P+RMTLARSAAKPAQALA+LET  +  +GFD+
Sbjct: 15  RGASIENTHVAHVAVVDASGRLLASFGDPSRMTLARSAAKPAQALAVLETGALERFGFDE 74

Query: 76  ADIALMCASHSSEDRHIARTRAMLSKIKAEEADLRCGGHPSLSEMVNRSWIKQDFIPTAV 135
           AD+ALMCASHSSE RHI RTR ML+K +A EADLRCGGHP LS+ V   W+K+DF P  V
Sbjct: 75  ADLALMCASHSSEARHIERTRQMLAKAQASEADLRCGGHPPLSDAVYIDWLKRDFKPDGV 134

Query: 136 CSNCSGKHVGMLAGARAIGAGTDGYHLPDHPMQGRVKRTVAELCDLDAGDVEWGTDGCNL 195
           CSNCSGKH GMLAGA++IGA  +GY  PDHP+Q RVK TVA++CDL    V+W TDGCNL
Sbjct: 135 CSNCSGKHAGMLAGAQSIGASMEGYERPDHPLQVRVKHTVADVCDLPDEAVQWATDGCNL 194

Query: 196 PTPAFPLDRLGRIYAKLASAADGSDAG-EGQSTRCAALAHIFRAMARHPEMVAGEGRYCT 254
           PTPAFPLDRL R++AKLA+A D   +G +  ++R +ALA I+RAM  +PE VAGEGR+CT
Sbjct: 195 PTPAFPLDRLARLFAKLAAAEDEVSSGAQSVTSRTSALARIYRAMTMYPEWVAGEGRFCT 254

Query: 255 MLMRAFDGALVGKLGADASYAIGVRASDATRQLGTDGALGISVKIEDGNLEMLYAVVTEL 314
            LM+AFDGALVGK+GAD SYAIGVRAS+ T++ G  GALG +VKIEDGN+ +LYAVV E+
Sbjct: 255 QLMQAFDGALVGKVGADGSYAIGVRASEQTKRAGAQGALGFAVKIEDGNVGILYAVVAEV 314

Query: 315 LERLGIGSPDVRSQLASFHHPQRVNTMGVTTGGVSFPFKLR 355
           L  L IG+P+ R++LA+FH P+ +NTMG+ T  ++F   L+
Sbjct: 315 LALLEIGTPEQRAKLAAFHAPKMLNTMGIQTSRITFSVALQ 355


Lambda     K      H
   0.319    0.134    0.397 

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: 469
Number of extensions: 14
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: 371
Length of database: 363
Length adjustment: 30
Effective length of query: 341
Effective length of database: 333
Effective search space:   113553
Effective search space used:   113553
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