GapMind for Amino acid biosynthesis

 

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

Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (uncharacterized)
to candidate AO353_16445 AO353_16445 succinyldiaminopimelate transaminase

Query= curated2:C6BUK3
         (388 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_16445
          Length = 399

 Score =  184 bits (468), Expect = 3e-51
 Identities = 132/395 (33%), Positives = 196/395 (49%), Gaps = 27/395 (6%)

Query: 10  LATLPPYLFAEIDRLKAEVAAQ-GVDIISLGIGDPDLPTPDFIIEALHKAAKNPVNHQYP 68
           L  L PY F ++  L   V        I+L IG+P   +P F+ EAL  A+       YP
Sbjct: 5   LNQLQPYPFEKLRALLGAVTPNPDKRPIALSIGEPKHRSPSFVAEAL--ASNLDQMAVYP 62

Query: 69  SYVGLLTFRQAVADWYKERFDVE---LDATKEVVSLIGSKEGIAHFPLAFVNPGDLVLVA 125
           + +G+   R+A+A W + RF V    +D  + V+ + G++E +  F    VN GD  L+ 
Sbjct: 63  TTLGIPALREAIAGWCERRFGVPSGWIDPARNVLPVNGTREALFAFTQTVVNRGDDALIV 122

Query: 126 SPN--YPVYPVASGFAGGEVEIVPLLEENDFLPNLDAISDEKWDKCKIFFVNYPNNPTSA 183
           SPN  Y +Y  A+  AG +   +P L+EN F P+ DA+SD+ W +C+I F+  P NPT A
Sbjct: 123 SPNPFYQIYEGAAFLAGAKPHYLPCLDENGFNPDFDAVSDDIWKRCQILFLCSPGNPTGA 182

Query: 184 TATPEFYAELVAKAKKHNVIIAADAAYTEVYYDEDKKPISILET---PGAKDV--AIEFH 238
               E   +L+A A +H+ +IAAD  Y+E+Y++E   P  +L      G KD    + FH
Sbjct: 183 LIPVETLKKLIALADEHDFVIAADECYSELYFNEQTPPPGLLSACVELGRKDFKRCVVFH 242

Query: 239 SLSKTYNMTGWRCGMAVGNASLVAGLGKIKENVDSGIFQAVQ-EAGIVALKEGEPYVKEF 297
           SLSK  N+ G R G   G+A ++ G   +      G    VQ +   VA    E +V+  
Sbjct: 243 SLSKRSNLPGLRSGFVAGDAEILKGF--LLYRTYHGCAMPVQTQLASVAAWNDEVHVRAN 300

Query: 298 RKIYKERRDCVIEALEKINISCKVPDASIFVWAKTPEGYTSSEFVSKLLKETGVVVTPG- 356
           R +Y+E+ D V+E L  + +  + PD   ++W    EG   + F   L  E  V V PG 
Sbjct: 301 RALYREKYDAVLEILSPV-MDVQRPDGGFYLWPNV-EG-DDAAFCRDLFVEEHVTVVPGS 357

Query: 357 ------NGFGESGEGYFRISLTVDTDRLKEAVSRI 385
                 +GF   G G  R++L        EA  RI
Sbjct: 358 YLSREVDGF-NPGAGRVRLALVAPLAECVEAAERI 391


Lambda     K      H
   0.317    0.136    0.398 

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: 440
Number of extensions: 30
Number of successful extensions: 5
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: 388
Length of database: 399
Length adjustment: 31
Effective length of query: 357
Effective length of database: 368
Effective search space:   131376
Effective search space used:   131376
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 (21.6 bits)
S2: 50 (23.9 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