GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Pseudomonas fluorescens FW300-N2E3

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate AO353_28160 AO353_28160 amidohydrolase

Query= curated2:B1YJ90
         (370 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_28160
          Length = 391

 Score =  218 bits (556), Expect = 2e-61
 Identities = 126/338 (37%), Positives = 192/338 (56%), Gaps = 12/338 (3%)

Query: 6   EMRRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGLTGNRTIGYR 65
           E+R  LH  PE G++E +T   + +++  +    V+    ET V   +K  T  R +G R
Sbjct: 17  ELRHHLHANPELGYQEVETSELVAERLTRWGY-AVTRGYAETAVIATLKKGTSPRVLGIR 75

Query: 66  ADIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVELPVMDDVVFL-FQPA 124
           AD+D LPI E TGLP+ S  PG MHACGHD H  + L     +      D  V L FQPA
Sbjct: 76  ADMDALPILEKTGLPYASRIPGKMHACGHDGHTVMLLAAAYALAHGHPFDGTVHLIFQPA 135

Query: 125 EEGPGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVHITIYGQS 184
           EEG  GA  MI+  + +K+    ++  H  P YPVG +  R G   ASA +V++TI+G+ 
Sbjct: 136 EEGLAGARRMIQEGVLQKFPCDAVFAAHNMPGYPVGKLGFRAGPFMASADQVNVTIHGKG 195

Query: 185 GHAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDAGIRENVIAGRALLD 244
           GH A PHL++D VV  A++IM LQTIVSR+++P + SVIT+G ++AG   NVI   A + 
Sbjct: 196 GHGAMPHLSVDPVVVCASIIMALQTIVSRNVSPQDMSVITVGAINAGKASNVIPDSAHML 255

Query: 245 GTMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVNDQRVVDKFSSFVKM 304
            ++R+LN    ++LE +++ +I     +FG   ++ +   Y  +VND+ +  +F+S V +
Sbjct: 256 MSVRSLNNAVRDRLESQIKRLIHAQAEAFGATAEIHYSADYPLLVNDEEMT-RFASQVAI 314

Query: 305 NANYIECDAAMT-------GEDFGFMLKEIPGMMFWLG 335
             +++  D  M         EDF + L++ PG    +G
Sbjct: 315 --DWLGEDEVMRDIVPFNGSEDFAYFLQQCPGCYLIIG 350


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: 355
Number of extensions: 18
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: 391
Length adjustment: 30
Effective length of query: 340
Effective length of database: 361
Effective search space:   122740
Effective search space used:   122740
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