GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Dechlorosoma suillum PS

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate Dsui_0989 Dsui_0989 amidohydrolase

Query= curated2:Q836H7
         (378 letters)



>FitnessBrowser__PS:Dsui_0989
          Length = 387

 Score =  226 bits (575), Expect = 1e-63
 Identities = 130/369 (35%), Positives = 201/369 (54%), Gaps = 16/369 (4%)

Query: 8   ELIAIRRQLHQIPEIGLEEKETQAFLLNEIDKMKQPYLQVRTW--QTGILVFIEGKNPQK 65
           EL A+RR +H  PE+  +E  T   +  E+++     ++V     +TG++  +   + ++
Sbjct: 11  ELTALRRDIHAHPELAFDESRTADIVARELERYG---IEVHRGIARTGVVGVLRNGSSKR 67

Query: 66  TIGWRADIDGLPIQEEVVSAFQSKRPGFMHACGHDFHMTIGLGVLKELSQQQP-DNNFLF 124
            IG RAD+D LP++E+     +S+  G MHACGHD H  + LG  + L++Q+  D   +F
Sbjct: 68  AIGLRADMDALPLEEKNEFPHRSRHEGKMHACGHDGHTALLLGAARWLAEQRNFDGTVVF 127

Query: 125 LFQPAEENEAGGMLMYEDHAFGEWLPDEFYALHVNPDLPVGTISTRVGTLFAATCEVNIT 184
           +FQPAEE+E G  +M ED  F ++  D  Y LH  P +P+G ++   G + A TC   I 
Sbjct: 128 IFQPAEESEGGAAVMIEDGLFEKFPVDAVYGLHNWPGIPLGEMAIMPGPVMAGTCAFEIA 187

Query: 185 LKGKGGHAAFPHQANDMVLAATNLIQQAQTIVSRNVDPVVGAVVTFGTFHAGTACNVIAE 244
           ++G G HAA PHQ  D ++A + L+Q  QT+VSR + P   AVV+   FHAG+A N+I +
Sbjct: 188 IRGHGCHAAMPHQGVDPIVAGSQLVQALQTVVSRTLHPCESAVVSVTQFHAGSAWNIIPD 247

Query: 245 EATLSGTIRTLTAETNEQTQRRIREISEGIAQSFQCEVTVHLDQKGYLPVVNE----PAC 300
           +A L GTIRT   E  E  +R I  +  G+A +   ++ V  D + Y P VN       C
Sbjct: 248 DAILRGTIRTFKPEVQETVERAIERLVSGVAAATGAQIGVTFDHR-YPPTVNSGPETEVC 306

Query: 301 TTNFIEYMSKQATVQFQQAPVAMTGEDFGYLLSKVPGTMFWLG---VASPYSLHSAKFEP 357
                  +  +  +    A  +M  EDF Y+L + PG   WLG        +LH+  ++ 
Sbjct: 307 RHAARAVLGHERVI--TDALPSMGAEDFAYMLREKPGCYVWLGNGPGTGGCTLHNPHYDF 364

Query: 358 NEEALLFGV 366
           N+EAL  G+
Sbjct: 365 NDEALAVGI 373


Lambda     K      H
   0.319    0.135    0.398 

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: 383
Number of extensions: 15
Number of successful extensions: 5
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: 378
Length of database: 387
Length adjustment: 30
Effective length of query: 348
Effective length of database: 357
Effective search space:   124236
Effective search space used:   124236
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 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