GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Desulfurobacterium atlanticum DSM 15668

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate WP_089323728.1 CHB58_RS08740 succinyldiaminopimelate transaminase

Query= BRENDA::O66630
         (387 letters)



>NCBI__GCF_900188395.1:WP_089323728.1
          Length = 387

 Score =  266 bits (680), Expect = 7e-76
 Identities = 148/374 (39%), Positives = 217/374 (58%), Gaps = 10/374 (2%)

Query: 8   LKVLPPYLFAELDRKKQEKIEQGVDVIDLGVGDPDMPTPKPIVEAAKKALENPENHKYPS 67
           L+ + PY   EL + K+   + G  + D G GDP  PT   I EA K A+  PE  +YP+
Sbjct: 5   LRNMKPYPMDELVKAKELLKKDGKKIYDFGTGDPKEPTAPFIREAVKTAI--PEVSQYPT 62

Query: 68  YVGKYEFRKAVADWYKRRFDVDLDPNTEVITLIGSKEGIAHFPLAFVNPGDI---VLCPD 124
             G+ + R+A++ W+KRRFDV+LD   E+I   GSKE I HFPL F++       V+   
Sbjct: 63  VKGRKDLREAISSWFKRRFDVELDSEKEIIPSAGSKEAIFHFPLVFIDADSDKKRVIFGT 122

Query: 125 PAYPVYRIGAIFAGGTPYTVPLKEENNFLPDLDSIPEDVAKKAKIIWINYPNNPTSAPPT 184
           PAYPVY  G +FA G P +  LK E  FL  LD +PE++ K+ KI+W+NYP+NPT A   
Sbjct: 123 PAYPVYERGTLFAQGIPTSYTLKYEEGFLLRLDKMPEEILKETKIVWLNYPHNPTGATAP 182

Query: 185 LEFYKKLVDWAKEYNVIIASDNAYSEIYTGQEKPPSILQVPGAKDVAIEFHSLSKTYNMT 244
           L +++ +    +EY++I+ SD  Y+EIY  +EKPPS LQV   K+  + FHSLSK   MT
Sbjct: 183 LSYFEDMYQICREYDIIMCSDECYTEIYF-EEKPPSALQV--GKENVVVFHSLSKRSGMT 239

Query: 245 GWRIGMAVGNKELVAGLGKVKTNVDSGQFGAVQDAGIVALNLPEEEVEKIRDVYRERKKI 304
           G+R G   G+  ++    + +++   G    +Q  G       E  VE+ R ++R++K+I
Sbjct: 240 GYRSGFVAGDSRIIQEYLRFRSSFGVGSPDFIQ-VGAREAWKDESHVEERRLIFRKKKEI 298

Query: 305 MTEALEKIGLEIYRSDYTFYLWIKVPEGYTSAEFVGRLIDEAGIVCTPGNGFGEYGEGYF 364
             +  ++ G E      +FY W+KVP G TS ++   L+ + GIV +PG  FG  GEG+F
Sbjct: 299 FEKFFKEEGFEFLDVKASFYFWVKVPFGLTSKDYAFHLL-KYGIVVSPGEFFGSGGEGFF 357

Query: 365 RISLTVPTERLLEA 378
           RI+L    +   EA
Sbjct: 358 RIALVPSVDECEEA 371


Lambda     K      H
   0.317    0.139    0.413 

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: 449
Number of extensions: 38
Number of successful extensions: 7
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: 387
Length of database: 387
Length adjustment: 30
Effective length of query: 357
Effective length of database: 357
Effective search space:   127449
Effective search space used:   127449
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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