GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Haloechinothrix alba DSM 45207

Align Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; EC 3.5.1.18; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase (uncharacterized)
to candidate WP_281251783.1 CHB84_RS20220 M20 family metallopeptidase

Query= curated2:Q0BUB7
         (383 letters)



>NCBI__GCF_900188115.1:WP_281251783.1
          Length = 379

 Score = 88.6 bits (218), Expect = 3e-22
 Identities = 102/324 (31%), Positives = 137/324 (42%), Gaps = 39/324 (12%)

Query: 56  GPRSG--PHLCFAGHTDVVPPGDAPWSVDAFAGEVHDGVLIGRGACDMKGAIASFV---A 110
           G R G  P L   GH DVVP     WSV  FAG V DG +IGRGACDMKG IA+ +    
Sbjct: 60  GDRDGSRPVLLINGHIDVVPARPQEWSVPPFAGVVKDGRVIGRGACDMKGGIAAAIEGLR 119

Query: 111 ACAARPDHPGT-ISLLITGDEEGVATDGTVRVLDWMRQAGEI-PDFCVVGEPTNPGRLGE 168
           AC      P   I   +  DEE     GT  +L    +AG I  D CVV EP        
Sbjct: 120 ACRDAGVRPAADIVFHLVADEETGGQHGTAALL----RAGRIQADACVVPEPNELS---- 171

Query: 169 VIKIGRRGSLNATLTVRGRQGHVAYPHRADNPLPRLVAALHALTTTRLDDGMEGFEPSSL 228
            I +  RG+L A + V GR GH + P    + +    A   AL      D     E   L
Sbjct: 172 -IGVAERGALLAEIEVFGRAGHGSDPAAVRSAVYDAAAITRALHCADFGDP----EHPML 226

Query: 229 QLTTVDV----GNPATNVIPEQAQARLNIRFNPLHRGDDLARWLRGIVQDHAPDAVIDIA 284
              T +V    G  A N++  Q    ++ R  P      +   +R ++ D   D  ID  
Sbjct: 227 GRPTCNVGVIRGGTAPNIVASQCDLSIDRRTLPGQTSSQVLDSVRDVI-DSLGD--IDYR 283

Query: 285 ISGEAFVTDPD-RDPRPGASHGIAAL-RMAIQRITGLSPRLDTGGGTSDARFITH--LCP 340
           ++   FV+  +     P  S+ + A  R A   + G          ++DARF+ +    P
Sbjct: 284 MTPTVFVSGSEIATDHPFVSYLLDACGRAAATEVRGSML-------STDARFMRNDLRIP 336

Query: 341 VVEFGLVGAT-MHQRDEAVAVRDL 363
            V +G       H  DE+V V +L
Sbjct: 337 TVVYGPGSMRHAHTADESVGVDEL 360


Lambda     K      H
   0.320    0.138    0.422 

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: 432
Number of extensions: 25
Number of successful extensions: 2
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: 383
Length of database: 379
Length adjustment: 30
Effective length of query: 353
Effective length of database: 349
Effective search space:   123197
Effective search space used:   123197
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 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