GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Desulfotomaculum ruminis DSM 2154

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_013842324.1 DESRU_RS11730 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000215085.1:WP_013842324.1
          Length = 392

 Score =  389 bits (998), Expect = e-112
 Identities = 181/380 (47%), Positives = 262/380 (68%)

Query: 9   ADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHG 68
           A RI+ LPPY+FAR++++ A+ +E GID+I LG+G+PD  TPQ ++    +    P+NH 
Sbjct: 6   AQRIKNLPPYLFARIEKVIAEKKEAGIDVISLGIGDPDIPTPQHIITELQKQALVPENHQ 65

Query: 69  YPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPS 128
           YP   G  S+R+A+ ++YNRR+ V LDP SE + L+GSKEG++H++  Y+NPGD+VLVP 
Sbjct: 66  YPSSVGMLSYRQAVADFYNRRFQVQLDPKSEVVALIGSKEGIAHISWCYLNPGDLVLVPD 125

Query: 129 PAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAP 188
           P YP +  G ++AG   + + L     +L D +AIPE+ ARKAK+++ NYP+NPTGA A 
Sbjct: 126 PGYPVYSGGAILAGAEPYYMPLTAARGFLPDFSAIPEDAARKAKMMFLNYPNNPTGAVAD 185

Query: 189 REFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMA 248
            +F+ E +AFA+KYEIL+ HD  Y+E++FDGY P S ++IPGAK++G+EF ++SK YNM 
Sbjct: 186 EKFYREAIAFAQKYEILICHDNAYSEVSFDGYSPLSFMQIPGAKEVGIEFSSVSKAYNMT 245

Query: 249 GWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDF 308
           GWR+G+ VGN  VI+ L   K+N+D G F A+Q AA   L  P   +    + YR RRD 
Sbjct: 246 GWRIGWAVGNAEVIEALGRFKSNIDSGQFQAVQYAAMAGLSGPQDAVTANNEIYRERRDI 305

Query: 309 LIQGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGYV 368
           ++ GL  +GW++ K KAT Y+W   P G  S  FA  ++ + GVV+TPGN +G  GEGY 
Sbjct: 306 VVDGLNAMGWNLEKPKATFYIWAPVPKGFTSASFAEFVIDKAGVVITPGNGYGEQGEGYF 365

Query: 369 RISLIADCDRLGEALDRIKQ 388
           RIS+    +R+ EAL+R+K+
Sbjct: 366 RISITMPKERIVEALERMKK 385


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: 488
Number of extensions: 19
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: 392
Length adjustment: 31
Effective length of query: 372
Effective length of database: 361
Effective search space:   134292
Effective search space used:   134292
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.

Links

Downloads

Related tools

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