GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Phaeobacter inhibens BS107

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (characterized)
to candidate GFF999 PGA1_c10160 amidohydrolase

Query= SwissProt::D5E0A1
         (375 letters)



>FitnessBrowser__Phaeo:GFF999
          Length = 388

 Score =  220 bits (561), Expect = 4e-62
 Identities = 131/372 (35%), Positives = 197/372 (52%), Gaps = 5/372 (1%)

Query: 5   EFVKIRRELHKIPELGFQEVKTQRFLLDYINTLPQERLEVKTWKTGLFVKVHGTNPT--K 62
           E    RR++H+ PE+ ++  +T   + + + T   + +     +TG+   + G + T  +
Sbjct: 13  EITAWRRDIHQNPEILYETHRTSASVAEKLRTFGCDEVVTGIGRTGVVGVIRGRSDTQNR 72

Query: 63  TIGYRADIDGLPITEETNYSFQSQHEGLMHACGHDMHMAIGLGVLTYFAQHEIKDNV-LF 121
            IG RAD+D LP+ E+T     SQ EG MHACGHD H A+ LG   Y A+    D   + 
Sbjct: 73  AIGLRADMDALPMAEDTGLPHASQIEGAMHACGHDGHTAMLLGAAKYLAETRNFDGTAVV 132

Query: 122 IFQPAEEGPGGAQPMLQSDIMKEWLPDFIFALHVAPEYPVGSIALKEGLLFANTSELFID 181
           IFQPAEEG  GA+ M +  +M  +  D ++A+H +P   +G  AL+ G + A+  E  I 
Sbjct: 133 IFQPAEEGGNGAEAMCKDGLMDRFGIDEVYAIHNSPGLELGKFALRPGPILASVDEFIIR 192

Query: 182 LKGKGGHAAYPHTTNDMVVAACQLVSQLQTIVARNVDPLDSAVITVGKIQ-GGTVQNIIA 240
           L+G+GGHAA P  T D  V  CQL++ LQ+IV+RNVDP+  AV++V   +      N+I 
Sbjct: 193 LQGRGGHAAKPQETVDTTVMMCQLITALQSIVSRNVDPVMQAVLSVTSAETSSKAYNVIP 252

Query: 241 ERARIEGTIRTLSPESMTRVKERIEAIVKGVEVGYQCETAIDYGCMYHQVYNHHEVTREF 300
           +RA ++GTIRT SP+    + ER+ A+  G+ + +     +++        N  E T   
Sbjct: 253 DRAEVKGTIRTHSPDVRAHIPERLRAVTAGIALTFGGSAEVEFVNGVPVTINDAEATGH- 311

Query: 301 MEFAKEQTDVDVIECKEAMTGEDFGYMLKDIPGFMFWLGVQSEYGLHHAKLQPHEGAIDI 360
              A      D  E   AM GEDF +ML++ PG M  +G  S  GLHH     ++ AI  
Sbjct: 312 AHAAALAVAGDCEEVALAMGGEDFSFMLEERPGAMIRVGNGSSAGLHHPAYDFNDDAIPA 371

Query: 361 AISLITKYFEHK 372
             S      E +
Sbjct: 372 GCSWFVTLIEQR 383


Lambda     K      H
   0.320    0.137    0.410 

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: 15
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: 375
Length of database: 388
Length adjustment: 30
Effective length of query: 345
Effective length of database: 358
Effective search space:   123510
Effective search space used:   123510
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: 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