GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Acidovorax sp. GW101-3H11

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate Ac3H11_3202 Metal-dependent amidase/aminoacylase/carboxypeptidase

Query= curated2:B1YJ90
         (370 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_3202
          Length = 397

 Score =  206 bits (523), Expect = 1e-57
 Identities = 125/345 (36%), Positives = 182/345 (52%), Gaps = 7/345 (2%)

Query: 7   MRRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGLTGNRTIGYRA 66
           +RR+LH+ PE  F+E +T A + +++  +    V+     TGV   ++   G++ +G RA
Sbjct: 30  LRRDLHEHPELSFQEHRTSAIVAERLAHWGYS-VTTGIAGTGVVGTLRKGQGSKALGIRA 88

Query: 67  DIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVELPVMDDVV-FLFQPAE 125
           D+D LPI EATGLP+ S + G MHACGHD H ++ L   R + E    D  +  +FQPAE
Sbjct: 89  DMDALPITEATGLPYASRNAGVMHACGHDGHTTVLLAAARFLAESGRFDGTLNLIFQPAE 148

Query: 126 EGPGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVHITIYGQSG 185
           E  GGA  MI   LFE++    ++GLH  P    G      G   AS  ++ IT+ G+ G
Sbjct: 149 EHGGGANRMIGEGLFERFPCDAVFGLHNWPCVGEGHFGCVTGPAMASVDQITITVRGKGG 208

Query: 186 HAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDAGIRENVIAGRALLDG 245
           H A PH T+D VVA A +I  LQT+VSR+++P++  V+T+G +  G   NV+     L  
Sbjct: 209 HGAAPHETVDPVVASAHIITALQTVVSRNVDPLDMGVVTVGSIHGGNAPNVVPESVELKL 268

Query: 246 TMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVNDQRVVDKFSSFVKMN 305
           T RA      E L+QR+  I R    SFG   ++ +   Y  V+N +   +   S  +  
Sbjct: 269 TARAFKPEVREILKQRIPAIARAQAESFGATAEVLYLPGYPAVLNHEAETELARSVARDT 328

Query: 306 ANYIECDAAM----TGEDFGFMLKEIPGMMFWLGVNNATSGLHQP 346
                 DA        EDF FML + PG   ++G N   + LH P
Sbjct: 329 FGDARVDAGFRPRTASEDFAFMLLKRPGSYVFVG-NGDGASLHSP 372


Lambda     K      H
   0.323    0.140    0.417 

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: 404
Number of extensions: 23
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: 370
Length of database: 397
Length adjustment: 30
Effective length of query: 340
Effective length of database: 367
Effective search space:   124780
Effective search space used:   124780
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 (21.9 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