GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Pseudomonas fluorescens FW300-N2E3

Align asparaginase (EC 3.5.1.1) (characterized)
to candidate AO353_25970 AO353_25970 asparaginase

Query= BRENDA::Q9RFN5
         (371 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_25970
          Length = 346

 Score =  406 bits (1043), Expect = e-118
 Identities = 200/339 (58%), Positives = 255/339 (75%), Gaps = 8/339 (2%)

Query: 16  RGGIVENSHRVHAAVVDAKGRLLYALGNPTRMTLARSAAKPAQALAILETEGVAGYGFDD 75
           RG  +EN+H  H AVVDA+GRLL   G+P+RMTLARSAAKPAQALA++ET  +  +G DD
Sbjct: 13  RGNSIENTHIAHVAVVDAQGRLLSGFGDPSRMTLARSAAKPAQALAVMETGALEQFGLDD 72

Query: 76  ADIALMCASHSSEDRHIARTRAMLSKIKAEEADLRCGGHPSLSEMVNRSWIKQDFIPTAV 135
           AD+ALMC SHSSE RHI R   ML+K  A EAD+RCGGHP +S+ V R+WIK DF+P  V
Sbjct: 73  ADLALMCGSHSSETRHIQRALGMLAKAGASEADMRCGGHPPISDEVYRAWIKSDFVPGPV 132

Query: 136 CSNCSGKHVGMLAGARAIGAGTDGYHLPDHPMQGRVKRTVAELCDLDAGDVEWGTDGCNL 195
           CSNCSGKH GMLA A+A+GA  +GYHLP HP+Q RV +TVAE+C++    ++W TDGCNL
Sbjct: 133 CSNCSGKHAGMLAAAQALGATLEGYHLPAHPLQQRVMQTVAEVCEVSGDAIQWATDGCNL 192

Query: 196 PTPAFPLDRLGRIYAKLASAADGSDAGEGQSTRCAALAHIFRAMARHPEMVAGEGRYCTM 255
           PTPAF LDRL  ++AK+ASAAD  ++   +S R A LA I+RAMA +PE+VAG+GR+CT 
Sbjct: 193 PTPAFALDRLALLFAKIASAADTGES--ARSPREAELARIYRAMATYPELVAGKGRFCTA 250

Query: 256 LMRAFDGALVGKLGADASYAIGVRASDATRQLGTDGALGISVKIEDGNLEMLYAVVTELL 315
           LM+AF+G LVGK+GADASYAIG+R       +    A GI+VK+EDGN  +LYAVV E+L
Sbjct: 251 LMKAFNGQLVGKVGADASYAIGIRG------VTDQQARGIAVKVEDGNQTVLYAVVCEVL 304

Query: 316 ERLGIGSPDVRSQLASFHHPQRVNTMGVTTGGVSFPFKL 354
            +L IG+   R+QL+++HHP  +NT+ V TG +   F L
Sbjct: 305 TQLNIGTAAQRAQLSAWHHPPMLNTVKVQTGRIELTFSL 343


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: 433
Number of extensions: 13
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: 371
Length of database: 346
Length adjustment: 29
Effective length of query: 342
Effective length of database: 317
Effective search space:   108414
Effective search space used:   108414
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