GapMind for catabolism of small carbon sources

 

Alignments for a candidate for amaD in Pseudomonas simiae WCS417

Align D-amino-acid oxidase (EC 1.4.3.3) (characterized)
to candidate GFF749 PS417_03805 D-amino acid oxidase

Query= BRENDA::A0PFJ3
         (386 letters)



>FitnessBrowser__WCS417:GFF749
          Length = 369

 Score = 80.5 bits (197), Expect = 7e-20
 Identities = 111/391 (28%), Positives = 161/391 (41%), Gaps = 50/391 (12%)

Query: 4   APPRRVVICGGGVVGACTAYFLATHAASPTVPTLVERCALACAASGKAGGFLA--LDWCD 61
           A  ++VVI GGGV+G  TA+ LAT   +     L+ER  L   +S   GG ++    W  
Sbjct: 2   AEQQQVVIVGGGVIGLLTAFNLATQGQAVV---LLERAGLGQESSWAGGGIVSPLYPWRY 58

Query: 62  STPALSRLARASFALHRRLADALGGADAYGFRP-VHTLSVL---LPPHPAA---SSSPPH 114
           S PA++ LA  S   + +LA  L      G  P VHT  +    L     A   ++    
Sbjct: 59  S-PAVTALAHWSQDFYPQLAQRLFAQT--GVDPEVHTTGLYWLDLDDEAEALAWAAREGR 115

Query: 115 PLLPPWVDPSASAAPPRELGTPDTTAQVH------PGLFT--KAVLAASGAEVVIGEVER 166
           PL    V  +  A P    G  +     +      P L    KA L       +  + E 
Sbjct: 116 PLSKVDVSAAHDAVPVLGGGYANAIYMANVANVRNPRLVKSLKAALLTLPGVTIHEQCEV 175

Query: 167 VAVAWD-GRVAGVVVKGRDGVLDADAVVLALGPWSGRLEVVSEVLDVSGLKAHSIVFRPR 225
                D G V GV     DG +  D VVLA G WSG      E+L   GL   S+   P 
Sbjct: 176 TGFLLDAGNVVGVSTA--DGAIFGDQVVLAAGAWSG------ELLGTLGL---SLPVEPV 224

Query: 226 EPEKVTPHCL--FLSYQPEPGAKMLDPEVYPRPTGEVYICGMSKDENPPDDPATITGEPD 283
           + + +   C   FLS       +       PR  G + I G + +    D   T T    
Sbjct: 225 KGQMILYKCASDFLSSMVLAKGRY----AIPRRDGHILI-GSTLEHEGFDKTPTETA--- 276

Query: 284 SIAMLHKIAGKVSSQLKKEEGAEVVAEQACYLPCTADGLPVIGEIPGVKGCYVATGHSCW 343
               L  +       +     AEVV   A   P + +G+P IG++PG KG ++  GH   
Sbjct: 277 ----LESLKASAVELIPALADAEVVGHWAGLRPGSPEGIPYIGQVPGFKGLWLNCGHYRN 332

Query: 344 GILNGPATGAALAELILDGKAKIVDLEPFSP 374
           G++  PA+     +L+L+ +A I+D  P++P
Sbjct: 333 GLVLAPASCQLFTDLLLE-RAPIIDPAPYAP 362


Lambda     K      H
   0.318    0.136    0.423 

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: 363
Number of extensions: 23
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 386
Length of database: 369
Length adjustment: 30
Effective length of query: 356
Effective length of database: 339
Effective search space:   120684
Effective search space used:   120684
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 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