GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Halomonas desiderata SP1

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_086509057.1 BZY95_RS05965 amidohydrolase

Query= curated2:Q836H7
         (378 letters)



>NCBI__GCF_002151265.1:WP_086509057.1
          Length = 386

 Score =  196 bits (497), Expect = 1e-54
 Identities = 137/381 (35%), Positives = 189/381 (49%), Gaps = 18/381 (4%)

Query: 7   EELIAIRRQLHQIPEIGLEEKETQAFLLNEIDKMKQPYLQVRTWQ---TGILVFIEGKN- 62
           E L A R   H+ PE   EE  T A +    + ++Q  L+V T     TG++  ++G+  
Sbjct: 10  ERLAAWRHDFHRHPETAFEEHRTGARIA---ELLRQAGLEVVTGLGGGTGVVAILDGRRG 66

Query: 63  PQKTIGWRADIDGLPIQEEVVSAFQSKRPGFMHACGHDFHMTIGLGVLKELSQQQPD--N 120
           P + IG RADID L ++E    A  S+ PG MHACGHD H T+ LG    L+   PD   
Sbjct: 67  PGRAIGLRADIDALDVEEANRFAHASQVPGKMHACGHDGHTTMLLGAAFALAAD-PDFAG 125

Query: 121 NFLFLFQPAEENEAGGMLMYEDHAFGEWLPDEFYALHVNPDLPVGTISTRVGTLFAATCE 180
              F+FQPAEE+E GG +M E+  F  +  +  Y LH  P L VG  +   G + AA   
Sbjct: 126 RVYFIFQPAEESEGGGRVMVEEGLFERFPMEAVYGLHNWPGLAVGEAAVHDGAVMAAFDV 185

Query: 181 VNITLKGKGGHAAFPHQANDMVLAATNLIQQAQTIVSRNVDPVVGAVVTFGTFHAGTACN 240
             + L G G HAA PH  +D +LAA  L+ Q Q +VSR   P   AV++   FHAG A N
Sbjct: 186 FTLRLSGHGCHAAMPHLGSDTLLAACQLVTQLQGLVSRETPPHQSAVLSVTQFHAGDAFN 245

Query: 241 VIAEEATLSGTIRTLTAETNEQTQRRIREISEGIAQSFQCEVTVHLD-QKGYLPVVNEP- 298
           VI E   L GT+R    E     +RR R+  E +A     ++ V LD Q  Y   +N P 
Sbjct: 246 VIPETVELRGTLRCFDGELRAYLERRFRQAVEALAGFH--DLRVELDYQSRYPATINAPE 303

Query: 299 --ACTTNFIEYMSKQATVQFQQAPVAMTGEDFGYLLSKVPGTMFWLG-VASPYSLHSAKF 355
             A     +E +     V  +  P +M  EDF ++L   PG   WLG      +LH+  +
Sbjct: 304 HAARCAGVLEALPGITRVH-RDLPPSMASEDFAFMLEACPGAYIWLGNGVESAALHNPHY 362

Query: 356 EPNEEALLFGVEAVSGFLKSL 376
           + N+     GV      +K+L
Sbjct: 363 DFNDAIAPLGVAYWQALVKTL 383


Lambda     K      H
   0.319    0.135    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: 353
Number of extensions: 21
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: 378
Length of database: 386
Length adjustment: 30
Effective length of query: 348
Effective length of database: 356
Effective search space:   123888
Effective search space used:   123888
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 10 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