GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Paraburkholderia bryophila 376MFSha3.1

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate H281DRAFT_06512 H281DRAFT_06512 hippurate hydrolase

Query= curated2:B1YJ90
         (370 letters)



>FitnessBrowser__Burk376:H281DRAFT_06512
          Length = 403

 Score =  202 bits (514), Expect = 1e-56
 Identities = 123/374 (32%), Positives = 194/374 (51%), Gaps = 13/374 (3%)

Query: 6   EMRRELHKIPEPGFKEFKTQAFILDQIRSYPEDRVSYDTFETGVFVRVKGLTGNRTIGYR 65
           ++RR+LH  PE  F+E +T   +  ++  +    VS     TGV   + G+  +  I  R
Sbjct: 20  KLRRDLHAYPELRFEEHRTADVVARELEEFGYT-VSRGLGGTGVVASLPGVNPHWGIVLR 78

Query: 66  ADIDGLPIEEATGLPFCSEHPGFMHACGHDVHASIALGLLRRIVELPVMDDVV-FLFQPA 124
           AD+D LPI+EA      S   G MHACGHD H  + LG  R +  +P +   V F+FQP 
Sbjct: 79  ADMDALPIQEANDFTHASCTHGIMHACGHDGHTVMLLGAARILRGMPQLPGSVHFVFQPG 138

Query: 125 EEGPGGAEPMIKSPLFEKYRPSEMYGLHVAPEYPVGTIASRPGVLFASAREVHITIYGQS 184
           EEG  GA  MI   LF +Y    ++G+H  P  P G    R G + A+     IT+ G+ 
Sbjct: 139 EEGGAGARKMIDDGLFVQYPTEAVFGMHNWPSLPGGHFGLRVGPIMAAGSRFRITVTGKG 198

Query: 185 GHAAFPHLTIDTVVAQAALIMQLQTIVSRSINPMNCSVITIGKVDAGIRENVIAGRALLD 244
            HAA PHL +D +    ++++  QTI +R  +P++ +VI++  + AG  +NVI   A L 
Sbjct: 199 AHAAQPHLGLDPIPLACSMVLHCQTIAARHKDPVDPAVISVCMIHAGDTDNVIPDSAELR 258

Query: 245 GTMRALNGTDMEKLEQRVRDIIRGIEASFGVKIDLQFGNRYYEVVNDQRVVDKFSSFVKM 304
           GT+R L+    +KL++ ++ +  G+ A+ G ++++ F   Y   +N +       + ++ 
Sbjct: 259 GTIRTLSSELQQKLQRDIQLMCEGLAAAHGAQVEVTFFQYYPATINTRAETQLCEAVIRE 318

Query: 305 ----NANYIECDAAMTGEDFGFMLKEIPGMMFWLG---VNNATSGLHQPTLNPDEEAIP- 356
                  + +  A MT EDFGFML+E PG    +G   V     GLH P  + +++ IP 
Sbjct: 319 TFGDERTHADVPANMTSEDFGFMLEERPGTYVLIGNAHVGETAPGLHNPKYDFNDDIIPA 378

Query: 357 ---FVINLLDHYFR 367
              + I L   YF+
Sbjct: 379 GVQYWITLAQQYFQ 392


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: 448
Number of extensions: 31
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: 403
Length adjustment: 30
Effective length of query: 340
Effective length of database: 373
Effective search space:   126820
Effective search space used:   126820
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