GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Thermovibrio ammonificans HB-1

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate WP_013537347.1 THEAM_RS02990 succinyldiaminopimelate transaminase

Query= BRENDA::O66630
         (387 letters)



>NCBI__GCF_000185805.1:WP_013537347.1
          Length = 387

 Score =  271 bits (693), Expect = 2e-77
 Identities = 152/376 (40%), Positives = 220/376 (58%), Gaps = 10/376 (2%)

Query: 8   LKVLPPYLFAELDRKKQEKIEQGVDVIDLGVGDPDMPTPKPIVEAAKKALENPENHKYPS 67
           ++ L  Y    L+R K+E   +G+ + D G GDP  PTP  I EA  +A+  PE  +YP+
Sbjct: 5   IRELKSYPMDRLNRAKEEIKRKGLKLFDFGTGDPKEPTPSFIREALIRAV--PEVSQYPT 62

Query: 68  YVGKYEFRKAVADWYKRRFDVDLDPNTEVITLIGSKEGIAHFPLAFVNPGDI---VLCPD 124
             G+ E R+A A W KRRF V+L+P  EVI   GSKE I H PL F+        V+   
Sbjct: 63  VKGRKELREAAAGWVKRRFGVELNPEAEVIPTAGSKEAIFHLPLVFIEAESDKRKVVFGT 122

Query: 125 PAYPVYRIGAIFAGGTPYTVPLKEENNFLPDLDSIPEDVAKKAKIIWINYPNNPTSAPPT 184
           PAYPVY  G +FAGG P+ V LK E NFL  LD +P  + ++ +I+WINYP+NPT A   
Sbjct: 123 PAYPVYLRGTLFAGGEPHPVELKFEENFLLRLDKLPRSLLEETRIVWINYPHNPTGASAP 182

Query: 185 LEFYKKLVDWAKEYNVIIASDNAYSEIYTGQEKPPSILQVPGAKDVAIEFHSLSKTYNMT 244
           L +++++    +E+ +I+ SD  Y +IY   E PPS+LQV   K+  + FHSLSK   MT
Sbjct: 183 LSYFEEVYGICREHGIILCSDECYVDIYF-TEPPPSVLQV--GKEGVLAFHSLSKRSGMT 239

Query: 245 GWRIGMAVGNKELVAGLGKVKTNVDSGQFGAVQDAGIVALNLPEEEVEKIRDVYRERKKI 304
           G+R G   G+ +LV    K +++        VQ A   A +  +  VE+ R +++E+ K+
Sbjct: 240 GYRSGFVAGDGKLVQEYLKYRSSFGVASQDFVQAAATAAWS-DDGHVEERRRIFKEKAKV 298

Query: 305 MTEALEKIGLEIYRSDYTFYLWIKVPEGYTSAEFVGRLIDEAGIVCTPGNGFGEYGEGYF 364
            +E  ++IGLE   ++ TFYLW+K P+G +  ++   L+ + GIV +PG  FG  GEG+F
Sbjct: 299 FSEFFKEIGLEFLPAEATFYLWVKTPKGVSGEKYALHLL-KYGIVVSPGEFFGRGGEGFF 357

Query: 365 RISLTVPTERLLEAAE 380
           RI+L        EA E
Sbjct: 358 RIALVPTLSECKEAVE 373


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: 405
Number of extensions: 27
Number of successful extensions: 6
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 Jul 25 2024. The underlying query database was built on Jul 25 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