GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Xanthobacter autotrophicus Py2

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_012115497.1 XAUT_RS17765 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000017645.1:WP_012115497.1
          Length = 406

 Score =  317 bits (811), Expect = 5e-91
 Identities = 157/385 (40%), Positives = 239/385 (62%), Gaps = 3/385 (0%)

Query: 7   TPADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKN 66
           T   RI++LPPYVF +++ +KA AR  G D++DLGMGNPD   P  V++   + +  P+ 
Sbjct: 3   TDFHRIRRLPPYVFEQVNRVKAAARNAGADIVDLGMGNPDLDAPAHVIEKLKETIGKPRT 62

Query: 67  HGYPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLV 126
             Y   +G    RRA   +Y RR+GV LDPD   +  LGSKEG +++A A   PGDV+L 
Sbjct: 63  DRYSASKGIPGLRRAQAAYYERRFGVKLDPDKHVVATLGSKEGFANMAQAITAPGDVILT 122

Query: 127 PSPAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGAT 186
           P+P+YP H  G ++AGG + S+ ++P  ++   +    +    K   +   YPSNPT   
Sbjct: 123 PNPSYPIHAFGFLMAGGVIRSVPVEPGPEFFHAMERAVQHSIPKPIAVVLCYPSNPTACV 182

Query: 187 APREFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYN 246
           A  EF++++VAFA+K +++++ DL YAEL FD   P S+L++PGA D+ VEF ++SKTY+
Sbjct: 183 ADLEFYKDVVAFAKKNDLIVLSDLAYAELYFDDTPPPSVLQVPGAMDVTVEFTSMSKTYS 242

Query: 247 MAGWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRR 306
           MAGWR+GF VGN  +I  L  +K+ LDYG +  +Q AA  AL  P   + E+++ Y+ RR
Sbjct: 243 MAGWRMGFAVGNERLIAALSRVKSYLDYGAYTPIQVAATAALNGPQECIAEMRETYKKRR 302

Query: 307 DFLIQGLGELGWDVPKTKATMYLWVKCPV---GMGSTDFALNLLQQTGVVVTPGNAFGVA 363
           D L++  G  G+ VP  +A+M+ W   P     MGS +FA  L+++  V V PG  FG  
Sbjct: 303 DALVESFGRAGFPVPSPRASMFAWAPIPEPFRAMGSVEFAKLLIEKADVAVAPGVGFGEH 362

Query: 364 GEGYVRISLIADCDRLGEALDRIKQ 388
           G+ +VRI+++ +  R+ +A   I++
Sbjct: 363 GDDFVRIAVVENEQRIRQAARNIRR 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: 453
Number of extensions: 17
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: 406
Length adjustment: 31
Effective length of query: 372
Effective length of database: 375
Effective search space:   139500
Effective search space used:   139500
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 Jul 25 2024. The underlying query database was built on Jul 25 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