GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Desulfovibrio zosterae DSM 11974

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_027722706.1 H589_RS0114540 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000425265.1:WP_027722706.1
          Length = 388

 Score =  379 bits (972), Expect = e-109
 Identities = 182/381 (47%), Positives = 263/381 (69%), Gaps = 1/381 (0%)

Query: 9   ADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHG 68
           ADR+  LPPY+FA++D+LKA+   QG+D+I LG+G+PD  TP+ +++A  +A Q+P NH 
Sbjct: 7   ADRLATLPPYLFAQIDKLKAEVAAQGVDIISLGIGDPDLPTPEFIIEALYKAAQNPVNHQ 66

Query: 69  YPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPS 128
           YP + G  +FR+A+ +WY  R+ V LD  +E + L+GSKEG++H  +A+VNPGD+VLV S
Sbjct: 67  YPSYVGLLTFRQAVADWYKERFNVELDAKTEVVSLIGSKEGIAHFPLAFVNPGDLVLVAS 126

Query: 129 PAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAP 188
           P YP +      AGG V  + L  END+L DL+ I +    KAK+++ NYP+NPT A A 
Sbjct: 127 PNYPVYPVASNFAGGEVEFVPLLEENDFLPDLSLIDDAKWDKAKVIFVNYPNNPTSAVAT 186

Query: 189 REFFEEIVAFARKYEILLVHDLCYAELAFD-GYQPTSLLEIPGAKDIGVEFHTLSKTYNM 247
            EF+EE++A A+K+ +++V D  Y E+ +D   +P S+LE PGAKD+ +EFH+LSKTYNM
Sbjct: 187 PEFYEELIAKAKKHNVIVVSDAAYTEVYYDENKKPLSILETPGAKDVAIEFHSLSKTYNM 246

Query: 248 AGWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRD 307
            GWR G  VGN  ++ GL  +K N+D GIF A+Q A   AL+  + Y+ E ++ Y+ RRD
Sbjct: 247 TGWRCGMAVGNASLVAGLGKIKENVDSGIFQAVQEAGIVALKEGEPYVKEFRKIYKERRD 306

Query: 308 FLIQGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGY 367
           ++I+ L ++       +A++++W K P G  S++F   LL++TGVVVTPGN FG +GEGY
Sbjct: 307 YVIEALEKINISCKVPEASIFVWAKTPKGYTSSEFVSKLLKETGVVVTPGNGFGESGEGY 366

Query: 368 VRISLIADCDRLGEALDRIKQ 388
            RISL  D DRL EA+ RI Q
Sbjct: 367 FRISLTVDTDRLKEAVSRISQ 387


Lambda     K      H
   0.321    0.140    0.427 

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: 460
Number of extensions: 20
Number of successful extensions: 2
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: 403
Length of database: 388
Length adjustment: 31
Effective length of query: 372
Effective length of database: 357
Effective search space:   132804
Effective search space used:   132804
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 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