GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Amycolatopsis halophila YIM 93223

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_157362617.1 AMYHA_RS25250 amidohydrolase

Query= curated2:B1YJ90
         (370 letters)



>NCBI__GCF_000504245.1:WP_157362617.1
          Length = 397

 Score =  173 bits (438), Expect = 8e-48
 Identities = 127/369 (34%), Positives = 178/369 (48%), Gaps = 15/369 (4%)

Query: 5   IEMRRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGLTGNRTIGY 64
           +  RR +H  PE   +E+ T   ++  +RS    +       TGV   V    G R +  
Sbjct: 28  VAWRRHIHANPELARREYGTTELVVRTLRSLGL-KPWVLPHGTGVVCDVG--EGERCVAL 84

Query: 65  RADIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVELPVMDDVV-FLFQP 123
           RAD+D LPI EATGLPF S   G  HACGHD H SI L     +V  P +   V  LFQP
Sbjct: 85  RADMDALPITEATGLPFASAVDGVAHACGHDAHTSILLATASALVAAPSLPGRVRLLFQP 144

Query: 124 AEEG-PGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVHITIYG 182
           AEE  PGGA   I +   E      ++GLH  P  PVG + +R G + ++A  V +++  
Sbjct: 145 AEEVMPGGALDSIAADALEGVE--RIFGLHCDPRLPVGKVGTRIGAITSAADLVELSLTS 202

Query: 183 QSGHAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDAGIRENVIAGRAL 242
             GH + PHLT D V A  ++I  L  ++SR ++P + +V+  G V AG   N +     
Sbjct: 203 PGGHTSRPHLTADLVHALGSVITGLPALISRRVDPRSGTVLVWGAVHAGEAANAVPEDGT 262

Query: 243 LDGTMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVNDQR----VVDKF 298
           L GT+R  +     +LE  V   I  + A  GV   L +      VV D      + D  
Sbjct: 263 LLGTLRTADIDVWRELEPLVGASIESLLAPTGVGYSLNYRRGVPPVVCDAESTGFLRDAV 322

Query: 299 SSFVKMNANYIECDAAMTGEDFGFMLKEIPGMMFWLGV---NNATSGLHQPTLNPDEEAI 355
           S+ +  +AN    + +  GEDFG+ L+ + G    LGV         LHQ T   DE A+
Sbjct: 323 SAALGQDAN-ASTEQSSGGEDFGWYLEHVDGAFARLGVWPGEGPQRDLHQGTFELDERAL 381

Query: 356 PFVINLLDH 364
           P  + L+ H
Sbjct: 382 PVGVRLMVH 390


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: 405
Number of extensions: 19
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 Jul 26 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