GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Bacteroides thetaiotaomicron VPI-5482

Align L-asparaginase (EC 3.5.1.1) (characterized)
to candidate 350054 BT0526 L-asparaginase I (NCBI ptt file)

Query= reanno::Pedo557:CA265_RS25090
         (339 letters)



>FitnessBrowser__Btheta:350054
          Length = 346

 Score =  355 bits (912), Expect = e-103
 Identities = 176/338 (52%), Positives = 243/338 (71%), Gaps = 3/338 (0%)

Query: 4   ILIIYTGGTIGMVNDPTNGMLIPFDFQQIKENVPELSRLDYDLDVHSFNPVLDSSNMDPE 63
           +L+IYTGGTIGM+ +P  G L  F+F  + ++VPEL R +Y +  + F+P LDSS+M+P 
Sbjct: 8   VLLIYTGGTIGMIENPETGALENFNFDHLLKHVPELKRFNYRISSYQFDPPLDSSDMEPA 67

Query: 64  IWKTLAELVYHKYDAYDGFVILHGSDTMAFTASALSFMLENLAKPVVLTGSQLPIGEIRT 123
            W  L +++ + YD +DGFVILHG+DTMA+TASALSFMLENL+KPV+LTGSQLPIG +RT
Sbjct: 68  YWAKLVKIINYNYDYFDGFVILHGTDTMAYTASALSFMLENLSKPVILTGSQLPIGTLRT 127

Query: 124 DAKENLITALEIAATKE-DGKALFPEVCIYFDAQLFRGNRSIKYNSEKFEAFRSPNYPIL 182
           D KENLITA+EIAA K  DG A+ PEVCI+F+  L RGNR+ K N+E F AFRS NYP L
Sbjct: 128 DGKENLITAIEIAAAKNPDGTAIVPEVCIFFENHLMRGNRTTKINAENFNAFRSFNYPPL 187

Query: 183 AEAGVHLQFHRNYILKA-TEGELKLHTNFNSNIGVLKLYPGITPQAVQAITD-SKVDAII 240
           A  G+H+++  N I K   +  LK H  F++N+ +L L+PGI  + + ++     + A++
Sbjct: 188 ARVGIHIKYEPNLIRKPDPDKPLKPHYLFDTNVVILTLFPGIQEEIIHSLLHVPGLKAVV 247

Query: 241 LETFGSGNTTTAQWFLDSLRQAILNGKIIIDISQCKKGSVQLGRYETSRELLKMGILSGY 300
           ++TFGSGN    +WF+  L++A   G II++I+QC  G+V++GRYET   LL+ G++SGY
Sbjct: 248 MKTFGSGNAPQKEWFIRELKEATDRGIIIVNITQCASGAVEMGRYETGMHLLEAGVISGY 307

Query: 301 DLTFEATVTKLMFVMGLGLSIEESRKLMEESLRGELTK 338
           D T E  VTKLMF++G GLS ++ R  M   L GE+TK
Sbjct: 308 DSTPECAVTKLMFLLGHGLSNKDIRYKMNSCLIGEITK 345


Lambda     K      H
   0.319    0.137    0.389 

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: 370
Number of extensions: 17
Number of successful extensions: 3
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: 339
Length of database: 346
Length adjustment: 29
Effective length of query: 310
Effective length of database: 317
Effective search space:    98270
Effective search space used:    98270
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 (21.7 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