GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Desulfallas geothermicus DSM 3669

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_092483207.1 BM299_RS08760 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_900115975.1:WP_092483207.1
          Length = 392

 Score =  392 bits (1007), Expect = e-114
 Identities = 182/380 (47%), Positives = 259/380 (68%)

Query: 9   ADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHG 68
           A RI+ LPPY+FAR+++L A+ +  G+D+I LG+G+PD  TP+ +++   +    P NH 
Sbjct: 6   AQRIKNLPPYLFARIEKLVAEKKAAGVDIISLGIGDPDMPTPEHIIEELQKQAAVPVNHQ 65

Query: 69  YPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPS 128
           YP   G  SFR+A+ +WY +R GV LDP +E + L+GSKEG++H++  Y+NPGD VLVP 
Sbjct: 66  YPSSVGMLSFRQAVADWYRKRSGVELDPATEVVSLIGSKEGIAHISWCYLNPGDTVLVPD 125

Query: 129 PAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAP 188
           P YP +  G ++AG   + + L  EN +L DL AIP EVARKAK+++ NYP+NPTGA A 
Sbjct: 126 PGYPVYSGGAILAGAEPYYMPLTAENKFLPDLNAIPAEVARKAKMMFINYPNNPTGAVAG 185

Query: 189 REFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMA 248
            EF+  ++ FA++Y IL+ HD  Y ++AFDGY+P S L+ PGAKD+G+EF ++SKTYNM 
Sbjct: 186 EEFYLAVIDFAKEYNILVCHDAAYCDMAFDGYKPPSFLQFPGAKDVGIEFLSVSKTYNMT 245

Query: 249 GWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDF 308
           GWR+G+  G+  V+  L  LK+N+D G F A+Q AA   L  P   +  +Q+ YR RRD 
Sbjct: 246 GWRIGWAAGHPGVVDALGRLKSNIDSGQFQAIQYAAMKGLTGPQDSVERMQKVYRERRDI 305

Query: 309 LIQGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGYV 368
           L+  L  +GW + K KAT Y+W   P G  S  FA  +L + GV++TPGN +G  GEG+ 
Sbjct: 306 LVDALNSMGWQLEKPKATFYVWAPVPAGYTSASFAEMVLDKCGVIITPGNGYGENGEGFF 365

Query: 369 RISLIADCDRLGEALDRIKQ 388
           RI+L  + DR+ EALDR+K+
Sbjct: 366 RIALTVEKDRMMEALDRMKK 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: 508
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.

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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