GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Magnetospirillum magneticum AMB-1

Align Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; EC 3.5.1.18; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase (uncharacterized)
to candidate WP_011384771.1 AMB_RS11990 acetylornithine deacetylase

Query= curated2:B2FIC0
         (375 letters)



>NCBI__GCF_000009985.1:WP_011384771.1
          Length = 404

 Score =  103 bits (257), Expect = 8e-27
 Identities = 104/346 (30%), Positives = 152/346 (43%), Gaps = 38/346 (10%)

Query: 49  NLWATHGLG-APVLVLLGHTDVVPTGPRESWTSDPFTPHIRDGVLYGRGAADMKGSVAAF 107
           N++AT G    P +VL GHTDVVP   ++ W+ DPF     DG LYGRG ADMK  +A  
Sbjct: 75  NIFATIGPSDVPGIVLSGHTDVVPVDGQD-WSRDPFHLVQADGKLYGRGTADMKSFIAIC 133

Query: 108 VVAAEQFVADHPDHPGTLAVLLTSDEEGDAIDGVRHVARLFAARGQRIDWCITGEPSSTA 167
           +  A QF A     P   A   + DEE   + GVR +    A    R   CI GEP+   
Sbjct: 134 LAMAPQFAAAPLRMPVHFA--FSYDEEVGCV-GVRRLIDDLAHLPVRPALCIVGEPTDMK 190

Query: 168 TLGDLLRVGRRGSLSAKLRVQGVQGHVAYPEKARNPIHQAAPALAELCARR--------W 219
            +     +G +G  S +  V+G + H A   +  N I  AA  +  L A +        +
Sbjct: 191 AV-----IGHKGKKSVRCHVEGHECHSALNHQGVNAIEIAAEMVTRLRALQRRIREQGPF 245

Query: 220 DDGYESFPPTSLQISNIHAGTGANNVIPGELDVDFNIRYNPHWDAPKLEAEI-------- 271
           D GY+  P T++    +  GT A N++P     +F IR  P  D   L AE+        
Sbjct: 246 DLGYQP-PYTTVHTGTMQGGT-ALNIVPKSCSFEFEIRNLPDHDPETLMAEVRGWAQDLV 303

Query: 272 ---TALLERHGLQYTLKWHRSGEPFYTPEGTLRAIARAVLAEHIGRAPEESTGGGTSDAR 328
               A+ E  G+  TL  H S       E  + A  R V A  +  A + S    T++A 
Sbjct: 304 PEMLAVSEASGI--TLDEHNSTPGLGMDE--MDAAVRLVCA--LSGANQTSKVAFTTEAG 357

Query: 329 FIAPLGAQCIEVGPVN-ASIHQVDENVRVDDLEALPGLYQRLVERL 373
                G   + +GP +    H+ DE + ++ +       +RL+  +
Sbjct: 358 LFQQAGIPAVVIGPGSITQAHRPDEFITLEQVAQCEDFLRRLLAHM 403


Lambda     K      H
   0.319    0.137    0.421 

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: 359
Number of extensions: 20
Number of successful extensions: 3
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: 375
Length of database: 404
Length adjustment: 30
Effective length of query: 345
Effective length of database: 374
Effective search space:   129030
Effective search space used:   129030
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 (21.7 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