GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Pedobacter sp. GW460-11-11-14-LB5

Align Isoaspartyl peptidase/L-asparaginase; Asparaginase-like protein 1; Asparaginase-like sperm autoantigen; Beta-aspartyl-peptidase; Glial asparaginase; Isoaspartyl dipeptidase; L-asparagine amidohydrolase; EC 3.4.19.5; EC 3.5.1.1 (characterized)
to candidate CA265_RS08130 CA265_RS08130 glycosylasparaginase

Query= SwissProt::Q8VI04
         (333 letters)



>FitnessBrowser__Pedo557:CA265_RS08130
          Length = 325

 Score =  144 bits (362), Expect = 4e-39
 Identities = 101/271 (37%), Positives = 148/271 (54%), Gaps = 22/271 (8%)

Query: 49  GIAKAATEGYNILKAGGSAVDAVEGAVTMLENDPEFNA-GYGSVLNADGDIEMDASIMDG 107
           GIA A  + + +L  GGSA+DAVE  V + E D    + GYG + + DG + +DA IMD 
Sbjct: 30  GIA-ANADAWKVLSTGGSALDAVEQGVWVPEADEHNQSVGYGGLPDRDGHVTLDACIMDE 88

Query: 108 KDLSAGAVSAVRCIANPVKLARLVMEKTPHCFLTGRGAEKFAADMGIPQ----TPA-EKL 162
              + GAV A+  I +P+ +AR VMEKTPH  L G GA +FA + G  +    TPA EK 
Sbjct: 89  LG-NCGAVLALEHIKHPISVARKVMEKTPHVMLAGDGALQFALEQGFKKENLLTPASEKA 147

Query: 163 ITE--RTKKHLEKEKLEKGAQKADCPK-------NSGTVGAVALDCKGNLAYATSTGGIV 213
             E  +T K+     +E    +   P+       N  T+G +A+D KGN++ A +T G+ 
Sbjct: 148 WKEWLKTAKYAPVMNIENQLYQKAAPQKLPGNQYNHDTIGMLAIDAKGNISGACTTSGMA 207

Query: 214 NKMVGRVGDSPCIGAGGYADNNLGAVSTTGHGESILKVNLARLALFHVEQGKTVDEAATL 273
            K+ GR+GDSP IGAG Y DN +G  ++TG GE +++   + L +  + QG T + A   
Sbjct: 208 YKLHGRIGDSPIIGAGLYVDNEVGGATSTGVGEEVVRNVGSFLVVELMRQGYTPEAACKE 267

Query: 274 ALDYMKSKLKGLG-----GLILINKTGDWVA 299
           A+  +  K          G + INK G++ A
Sbjct: 268 AVMRIIKKKPETAKNIQVGFLAINKKGEYGA 298


Lambda     K      H
   0.313    0.131    0.379 

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: 269
Number of extensions: 18
Number of successful extensions: 4
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: 333
Length of database: 325
Length adjustment: 28
Effective length of query: 305
Effective length of database: 297
Effective search space:    90585
Effective search space used:    90585
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