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_086508853.1 BZY95_RS04885 amidohydrolase

Query= curated2:B1YJ90
         (370 letters)



>NCBI__GCF_002151265.1:WP_086508853.1
          Length = 392

 Score =  235 bits (600), Expect = 1e-66
 Identities = 139/356 (39%), Positives = 199/356 (55%), Gaps = 6/356 (1%)

Query: 6   EMRRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGLTGNRTIGYR 65
           E+R ++H  PE GF+E +T A + +++R++  D V  D   TGV   +KG    R IG R
Sbjct: 16  EIRHDIHAHPELGFEETRTAALVAEKLRAWDIDEVHTDIAGTGVVGVIKGREEGRCIGLR 75

Query: 66  ADIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVEL-PVMDDVVFLFQPA 124
           AD+D LPI+EAT LP+ S H G MHACGHD H +I LG  R + E       VV +FQPA
Sbjct: 76  ADMDALPIQEATDLPYASRHAGKMHACGHDGHTTILLGAARYLAETRDFAGTVVLIFQPA 135

Query: 125 EEGPGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVHITIYGQS 184
           EEG GGA  M+   LFE++   E+YG+H  P    G ++  PG   A A    I I G+ 
Sbjct: 136 EEGLGGARRMLADRLFERFPCDEIYGIHNDPTSDPGKVSVTPGPAMAGATFFDIVIEGKG 195

Query: 185 GHAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDAGIRENVIAGRALLD 244
            HAA PH + D V+  A LI QLQT+VSR+ +P +  V+++ +V AG   NVI   A L 
Sbjct: 196 AHAAMPHQSNDPVIVAAELIHQLQTVVSRNTSPTSPLVLSVTQVHAGSAYNVIPNEATLA 255

Query: 245 GTMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVNDQRVVDKF---SSF 301
           GT+R  +    E+  +R+R + +G+E +  VKI +   N +  +VN+      +   ++ 
Sbjct: 256 GTIRYFDDEVCERTHERIRLLCKGLELAHEVKIRVDLRNIFNVLVNEPGCAGAYVAAAAE 315

Query: 302 VKMNANYIECDAAMTG-EDFGFMLKEIPGMMFWLGVNNATSGLHQPTLNPDEEAIP 356
           V    N    D  +TG EDF  ML+ +PG   W+G +  +  LH P    D+  +P
Sbjct: 316 VVGEENAALVDRLVTGSEDFADMLQVVPGAYCWVG-HAGSVPLHNPGYVLDDGILP 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: 368
Number of extensions: 16
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: 392
Length adjustment: 30
Effective length of query: 340
Effective length of database: 362
Effective search space:   123080
Effective search space used:   123080
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 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