GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Phaeobacter inhibens BS107

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate GFF1000 PGA1_c10170 putative hippurate hydrolase

Query= curated2:B1YJ90
         (370 letters)



>FitnessBrowser__Phaeo:GFF1000
          Length = 387

 Score =  227 bits (579), Expect = 4e-64
 Identities = 136/358 (37%), Positives = 202/358 (56%), Gaps = 14/358 (3%)

Query: 8   RRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGLTGN--RTIGYR 65
           RR++H+ PE  F+  +T A + ++++ +  D +      TGV   +KG + +  + IG R
Sbjct: 18  RRDIHENPEILFETHRTSALVAEKLKEFGCDEIVTGIGRTGVVGVIKGKSDSSGKVIGLR 77

Query: 66  ADIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVELPVMDD-VVFLFQPA 124
           AD+D LPI E TGL + S+  G MHACGHD H ++ LG  + + E    D  VV +FQPA
Sbjct: 78  ADMDALPIHEQTGLEYASKTDGAMHACGHDGHTAMLLGAAKYLSETRNFDGTVVVIFQPA 137

Query: 125 EEGPGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVHITIYGQS 184
           EEG GG + M    + +++   E+YG+H  P  PVG+ A RPG  FA+  +  IT  G+ 
Sbjct: 138 EEGGGGGKEMCDDGMMDRWNIQEVYGMHNWPGRPVGSFAIRPGAFFAATDQFDITFEGRG 197

Query: 185 GHAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDAGIRE-NVIAGRALL 243
           GHAA P  TIDT V  A  ++ LQTI SR+ +P++  V+++   +   +  NVI     +
Sbjct: 198 GHAAKPQETIDTTVMSAQAVLALQTIASRNADPVHQIVVSVTSFETSSKAFNVIPQSVHI 257

Query: 244 DGTMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVNDQRVVDKFSSFVK 303
            GT+R ++G   +  E+R+ +I  GI A+FG   D+ +   Y  +VN     D+ + F  
Sbjct: 258 KGTVRTMSGEMRDLAEKRINEICDGIAATFGGTADVTYHRGYPVMVNH----DEQTEFAA 313

Query: 304 MNANYIE--CDAA---MTGEDFGFMLKEIPGMMFWLGVNNATSGLHQPTLNPDEEAIP 356
             A  I   CD A   M GEDF FML+E PG    +G N  T+ +H P  N ++EAIP
Sbjct: 314 KVARDISGGCDDAPLVMGGEDFAFMLEERPGAYILVG-NGDTAAVHHPEYNFNDEAIP 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: 381
Number of extensions: 22
Number of successful extensions: 6
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: 387
Length adjustment: 30
Effective length of query: 340
Effective length of database: 357
Effective search space:   121380
Effective search space used:   121380
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 09 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