GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Leptospirillum ferrooxidans C2-3

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_014448518.1 LFE_RS01525 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000284315.1:WP_014448518.1
          Length = 395

 Score =  407 bits (1045), Expect = e-118
 Identities = 191/383 (49%), Positives = 264/383 (68%)

Query: 9   ADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHG 68
           + RI+ LPPY+FAR+DE K +A  +G+D+I+LG+G+PD  T  P+V+AA  AL  P++H 
Sbjct: 8   SQRIKSLPPYLFARIDEKKREAMAKGMDIINLGIGDPDTPTLPPIVEAARIALGRPEHHQ 67

Query: 69  YPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPS 128
           YP +EG  SFR +I +WY +R+ V LDP +E L L+GSKEG+ H+ +A+++PGD VLVP 
Sbjct: 68  YPSYEGMLSFRESIAHWYKKRFLVDLDPHTEVLGLIGSKEGIGHMPLAFIDPGDTVLVPE 127

Query: 129 PAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAP 188
           P YP +  G + AGG  + + +   N +L DL+AIP+ V R+ KI++ NYP+NPTGA AP
Sbjct: 128 PGYPVYHAGTLFAGGETYYMPILESNGFLPDLSAIPDSVYRRTKIMFINYPNNPTGAVAP 187

Query: 189 REFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMA 248
             FF E++  A KY  ++ HD  Y+E+ FDG  P S L  PGAK++G+EFH+LSKT+NM 
Sbjct: 188 DSFFAEVIEKATKYGFIVAHDAAYSEIYFDGNAPKSFLSFPGAKEVGIEFHSLSKTFNMT 247

Query: 249 GWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDF 308
           GWRVGF VGN  V+ GL  +K+N+D GIF ALQ A+  A+ LPD ++  ++  Y+ RRD 
Sbjct: 248 GWRVGFAVGNASVLAGLGKIKSNMDSGIFQALQEASIAAMALPDFWMENLRSMYQERRDV 307

Query: 309 LIQGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGYV 368
           L+ GL   G  V    A+ YLW   P GM S + +L LL +TG+V TPGN FG++GEGYV
Sbjct: 308 LVSGLRTAGLRVIPPGASFYLWAGIPAGMKSEEASLALLSRTGIVATPGNGFGISGEGYV 367

Query: 369 RISLIADCDRLGEALDRIKQAGI 391
           R +L  D  RL EA+DRI   G+
Sbjct: 368 RFALTVDTPRLKEAIDRIVNEGL 390


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: 507
Number of extensions: 25
Number of successful extensions: 1
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: 395
Length adjustment: 31
Effective length of query: 372
Effective length of database: 364
Effective search space:   135408
Effective search space used:   135408
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