GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Pseudomonas simiae WCS417

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate GFF2657 PS417_13545 arginine aminotransferase

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__WCS417:GFF2657
          Length = 664

 Score =  204 bits (518), Expect = 8e-57
 Identities = 125/361 (34%), Positives = 193/361 (53%), Gaps = 5/361 (1%)

Query: 25  AQHEDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKADF 84
           +Q ED+I L++G PDF TP  +  AA  A+ E  T YT   G   LR+A+     K    
Sbjct: 29  SQGEDIIILSVGDPDFATPSFITDAAVSALREGDTHYTEIPGRPALREAIAARYSKTLAR 88

Query: 85  NYDAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIVDTTS 144
              AE+ +I   GA  A+      +L  GDEV++  P+Y  YE  +   GA  V V  + 
Sbjct: 89  ALSAEN-VITVAGAQNALFVTSLCLLQAGDEVLVLDPMYVTYEATLKASGATLVRVPCSP 147

Query: 145 H-GFKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSDEIY 203
             GF+L A+L+  A+TP T+ +    P+NPTGV L+ +EL++IA L   R+++V+ DE+Y
Sbjct: 148 ESGFRLDAQLLGAAITPRTRAIFFSNPNNPTGVVLNLQELQAIADLAIARDLWVVVDEVY 207

Query: 204 SELTYDRPHYSIATY--LRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQYNV 261
             L +D  ++S+A    + ++ +VI  LSKSH+MTGWRIG++ A   +  H   +    +
Sbjct: 208 ESLVFDGEYHSLAALPGMAERCVVIGSLSKSHAMTGWRIGWIIATPQMVAHAETLVLSML 267

Query: 262 SCASSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSM-GLDVVKPSGAFYIFPS 320
                   +AA  AV    D    MRE Y++R D V   L +  G+ V  P    ++   
Sbjct: 268 YGLPGFVMEAATAAVLAHDDVTQGMREIYRRRRDLVMAGLSACPGIKVQAPQAGMFVLVD 327

Query: 321 IKSFGMTSFDFSMALLEDAGVALVPGSSFSTYGEGYVRLSFACSMDTLREGLDRLELFVL 380
           ++  G+ S DF+  L  +AGV+++  ++F    +G+VRLSF    + L E   R+  FV 
Sbjct: 328 VRGTGLGSLDFAWRLFREAGVSVLDAAAFGAPAQGFVRLSFTLGEERLSEACQRIAHFVA 387

Query: 381 K 381
           K
Sbjct: 388 K 388


Lambda     K      H
   0.319    0.135    0.388 

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: 451
Number of extensions: 16
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: 393
Length of database: 664
Length adjustment: 34
Effective length of query: 359
Effective length of database: 630
Effective search space:   226170
Effective search space used:   226170
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: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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