GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Bacteroides thetaiotaomicron VPI-5482

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate 353461 BT3935 aminotransferase (NCBI ptt file)

Query= BRENDA::O66630
         (387 letters)



>FitnessBrowser__Btheta:353461
          Length = 393

 Score =  297 bits (761), Expect = 3e-85
 Identities = 160/382 (41%), Positives = 223/382 (58%), Gaps = 3/382 (0%)

Query: 5   SDRLKVLPPYLFAELDRKKQEKIEQGVDVIDLGVGDPDMPTPKPIVEAAKKALENPENHK 64
           ++RL  +  Y F++  ++  +   +G DVI LG+G PDMP  K  +E       +P  H 
Sbjct: 13  AERLASVSEYYFSKKLKEVAQMNAEGKDVISLGIGSPDMPPSKVTIETLCNNAHDPNGHG 72

Query: 65  YPSYVGKYEFRKAVADWYKRRFDVDLDPNTEVITLIGSKEGIAHFPLAFVNPGDIVLCPD 124
           Y  YVG  E RK  A WY+R + V+L+PNTE+  LIGSKEGI H  LAFVNPG+ VL P+
Sbjct: 73  YQPYVGIPELRKGFAAWYQRWYGVELNPNTEIQPLIGSKEGILHVTLAFVNPGEQVLVPN 132

Query: 125 PAYPVYRIGAIFAGGTPYTVPLKEENNFLPDLDSIPEDVAKKAKIIWINYPNNPTSAPPT 184
           P YP Y   +   G    +  LKEE+ ++PD +++ +    + K++W NYPN PT A  T
Sbjct: 133 PGYPTYTSLSKILGAEVISYDLKEEDGWMPDFEALEKMDLNRVKLMWTNYPNMPTGANAT 192

Query: 185 LEFYKKLVDWAKEYNVIIASDNAYSEIYTGQEKPPSILQVPGAKDVAIEFHSLSKTYNMT 244
            E Y++LVD+A+  N++I +DN YS I    EKP SIL VPGAK+  IEF+S+SK++NM 
Sbjct: 193 PELYERLVDFARRKNIVIVNDNPYSFIL--NEKPISILSVPGAKECCIEFNSMSKSHNMP 250

Query: 245 GWRIGMAVGNKELVAGLGKVKTNVDSGQFGAVQDAGIVALNLPEEEVEKIRDVYRERKKI 304
           GWRIGM   N E V  + KVK+N+DSG F A+Q A   AL    +  E     YR R+ +
Sbjct: 251 GWRIGMLASNAEFVQWILKVKSNIDSGMFRAMQLAAATALEAEADWYEGNNHNYRGRRHL 310

Query: 305 MTEALEKIGLEIYRSDYTFYLWIKVPEGYTSA-EFVGRLIDEAGIVCTPGNGFGEYGEGY 363
             E ++ +G     +    +LW K+P       E   +++ +A +  TPG  FG  G  +
Sbjct: 311 AGEIMKTLGCTYDENQVGMFLWGKIPASCKDVEELTEKVLHQARVFITPGFIFGSNGARF 370

Query: 364 FRISLTVPTERLLEAAERIKNL 385
            RISL     +L EA ERIK L
Sbjct: 371 IRISLCCKDAKLAEALERIKKL 392


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: 462
Number of extensions: 17
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: 387
Length of database: 393
Length adjustment: 31
Effective length of query: 356
Effective length of database: 362
Effective search space:   128872
Effective search space used:   128872
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 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