GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Cereibacter sphaeroides ATCC 17029

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_002720066.1 RSPH17029_RS07865 M20 family metallopeptidase

Query= curated2:B1YJ90
         (370 letters)



>NCBI__GCF_000015985.1:WP_002720066.1
          Length = 388

 Score =  214 bits (544), Expect = 4e-60
 Identities = 124/366 (33%), Positives = 194/366 (53%), Gaps = 15/366 (4%)

Query: 2   EYAIEM---RRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGLTG 58
           +YA EM   RR LH+ PE  F    T AFI +++R++  D +      +G+   ++G   
Sbjct: 9   DYAEEMTAWRRHLHRHPELRFDCQNTAAFIAERLRAFGVDEIHEGIATSGLVAIIEGQGE 68

Query: 59  NRTIGYRADIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVELP-VMDDV 117
             TIG RAD+D LPIEE TG  + S  PG MHACGHD H ++ LG  R + E       V
Sbjct: 69  GPTIGLRADMDALPIEELTGADYASTVPGRMHACGHDGHVTMLLGAARYLAETRRFAGRV 128

Query: 118 VFLFQPAEEGPGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVH 177
             LFQPAEE  GG E M++  + +++  S++YG+H AP  P+G   + PG L A+     
Sbjct: 129 ALLFQPAEEDGGGGEVMVREGVMDRFGISQVYGIHNAPNVPLGRFVTAPGPLMAAVDTAT 188

Query: 178 ITIYGQSGHAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDAGIRENVI 237
           + + G+ GH A PH T+D VVA   ++  LQTI+SR++  ++  V+++ ++  G   N+I
Sbjct: 189 VRVIGKGGHGATPHETVDPVVAIVGMVSALQTIISRNLYTLDDLVLSVTQIHTGSASNII 248

Query: 238 AGRALLDGTMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVND------ 291
                   T+R       + + +R  +I+ G  A++GV++++ +   Y   VND      
Sbjct: 249 PEDGWFCATIRTFTPEVRDLVRRRFHEIVEGHAAAYGVRVEIDYELGYPPTVNDPAKAGF 308

Query: 292 -QRVVDKFSSFVKMNANYIECDAAMTGEDFGFMLKEIPGMMFWLGVNNATSGLHQPTLNP 350
              V  + +    + AN    +  M  EDF +ML+  PG   +LG     +GLH P  + 
Sbjct: 309 AAEVAAEIAGEAGVEAN---ANREMGSEDFAYMLEARPGAYLFLGTGPG-AGLHHPAYDF 364

Query: 351 DEEAIP 356
           ++ A P
Sbjct: 365 NDAASP 370


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: 388
Number of extensions: 24
Number of successful extensions: 3
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: 388
Length adjustment: 30
Effective length of query: 340
Effective length of database: 358
Effective search space:   121720
Effective search space used:   121720
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 Jul 25 2024. The underlying query database was built on Jul 25 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