GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Pseudomonas putida KT2440

Align Probable L-asparaginase periplasmic; L-ASNase; EC 3.5.1.1; L-asparagine amidohydrolase (uncharacterized)
to candidate PP_1160 PP_1160 Asparaginase family protein

Query= curated2:P43843
         (349 letters)



>FitnessBrowser__Putida:PP_1160
          Length = 329

 Score =  153 bits (386), Expect = 7e-42
 Identities = 108/322 (33%), Positives = 166/322 (51%), Gaps = 21/322 (6%)

Query: 22  ADLPNITILATGGTI---AGSGQSSVNSAYKAGQLSIDTLIEAVPEMKNIANIKGEQIVK 78
           + LP ++I   GGT+   AG+    V  +     L  +  +  VP+++ +A +    +  
Sbjct: 5   SSLPRLSIATLGGTVSMRAGAVGDGVTPS-----LDCERQLLQVPQLREMAQLNVASLCL 59

Query: 79  IGSQDMNDEVWLK-LAKAINAQCKSTDGFVITHGTDTMEETAYFLDLTVKCEKPVVLVGA 137
           + S  +     L+ LA A     +     V++ GTD++EETAYFLDL    + P+V+ GA
Sbjct: 60  LPSASLGFATLLEVLAWARGEVERGAQALVLSQGTDSLEETAYFLDLLWPFDVPLVMTGA 119

Query: 138 MRPATEKSADGPLNLYNAVVVAADKKSSGRGVLVAMNNEVLGARDVTKTSTTAVQTFHSP 197
           MR A++   DGP NL  A  VA  + S GRGVLV MN++V  A  V KT++ A+  F SP
Sbjct: 120 MRSASQPGNDGPANLLAAAQVALAQDSRGRGVLVVMNDQVHCAARVRKTASLAMAAFESP 179

Query: 198 NYGSLGYIHNSKVDYERSPESKHTINTPFNVEKLDSLPKVGIIYAYSNAPVEPLNALLNA 257
             G LG +    V Y   P  +  +  P+  ++     +V ++ A  +A    L A+   
Sbjct: 180 GCGPLGDVVEGVVLYRHPPGRRKVLPLPYRTDQ-----RVALLEACLDADTALLQAVATL 234

Query: 258 GYQGIVSAGVGNGNVNAAHLDRLEKAAKDSVVVVRSSRVPTGYTTR------DAEVDDSK 311
           GY+G+V AG G G+V+A+  + LE  A    V+V ++R   G T R       AE+D  K
Sbjct: 235 GYEGLVIAGFGAGHVSASWSEVLEHLAPTLPVMV-ATRTGRGLTARATYGFAGAEIDLQK 293

Query: 312 YGFVASGTLNPQKARVLLQLAL 333
            G   +G L P+K R+LL L +
Sbjct: 294 KGVYMAGQLCPRKCRILLWLLI 315


Lambda     K      H
   0.313    0.130    0.361 

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: 223
Number of extensions: 12
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: 349
Length of database: 329
Length adjustment: 28
Effective length of query: 321
Effective length of database: 301
Effective search space:    96621
Effective search space used:    96621
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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