GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Archaeoglobus veneficus SNP6

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_013684737.1 ARCVE_RS10425 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000194625.1:WP_013684737.1
          Length = 384

 Score =  360 bits (923), Expect = e-104
 Identities = 178/379 (46%), Positives = 255/379 (67%), Gaps = 3/379 (0%)

Query: 9   ADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHG 68
           A+R+Q+LPPY+FA LD +K K   +G+ LID G+G+PD  TP  +V+A  +A++  +N  
Sbjct: 5   AERLQRLPPYLFAELDAMKRKKLREGVKLIDFGVGDPDLPTPPHIVEAMKKAVEKVENQK 64

Query: 69  YPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPS 128
           YP +EG  SFR A+ ++Y RR GV LDP+ E + L+GSKEG++HL +AYVN GD+VL P 
Sbjct: 65  YPSYEGMLSFREAVADFYKRRKGVDLDPEKEVIALIGSKEGIAHLPLAYVNSGDIVLCPD 124

Query: 129 PAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAP 188
           P YP +    ++A G  + + LK EN +L DL AIP++VARKAKI++ NYP+NPT + A 
Sbjct: 125 PGYPVYPSSAILADGKPYFMPLKKENGFLPDLQAIPDDVARKAKIMFLNYPNNPTASVAE 184

Query: 189 REFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMA 248
           ++F +E++ F    +I+L HD  Y+E+ FD Y+  S LE+ G + + +EF++LSKTYNM 
Sbjct: 185 KDFIKEVIEFCNDRKIVLAHDAAYSEITFD-YRARSFLEV-GIEGV-IEFNSLSKTYNMT 241

Query: 249 GWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDF 308
           GWR+GF  G   V+ GL  +KTN+D G+F A+Q AA  AL   D  + E  + Y+ RRD 
Sbjct: 242 GWRIGFAAGCPEVLAGLLKVKTNVDSGVFQAVQEAAIAALTGSDEVIDENNRIYKERRDT 301

Query: 309 LIQGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGEGYV 368
           LI+GL E+G +  K KAT Y+W + P G  S +F   LL   G++VTPG  FG  GEG+V
Sbjct: 302 LIEGLKEVGLNAEKPKATFYVWCEVPEGYTSMEFTKKLLNDAGILVTPGIGFGEHGEGFV 361

Query: 369 RISLIADCDRLGEALDRIK 387
           R +L  D   + EA++R+K
Sbjct: 362 RFALTRDVGVIQEAVERLK 380


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: 461
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: 384
Length adjustment: 31
Effective length of query: 372
Effective length of database: 353
Effective search space:   131316
Effective search space used:   131316
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