GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Hyphomicrobium sulfonivorans WDL6

Align Aromatic-amino-acid transaminase (EC 2.6.1.57) (characterized)
to candidate WP_068464880.1 APY04_RS16090 histidinol-phosphate transaminase

Query= reanno::BFirm:BPHYT_RS14905
         (370 letters)



>NCBI__GCF_001541235.1:WP_068464880.1
          Length = 367

 Score =  238 bits (608), Expect = 1e-67
 Identities = 130/335 (38%), Positives = 196/335 (58%), Gaps = 1/335 (0%)

Query: 37  VKLASNENPLGMPESAQRAMAQAASELGRYPDANAFELKAALSERYGVPADWVTLGNGSN 96
           +KL+SNE P G    A  A   A + L RYPD  A +L+ A++ RYG+    +  G GS+
Sbjct: 32  IKLSSNETPFGPSPKAVEAYRAADAALERYPDGAATKLREAIARRYGLNPARIICGAGSD 91

Query: 97  DILEIAAHAFVEKGQSIVYAQYSFAVYALATQGLGARAIVVPAVKYGHDLDAMLAAVSDD 156
           ++L + AHA++ +G   +Y Q+ F +Y +     GA  +V P      D+DA+L  V++ 
Sbjct: 92  ELLTMLAHAYLGEGDEAIYTQHGFLLYRIIILANGATPVVAPETGLRTDIDAILNRVTER 151

Query: 157 TRLIFVANPNNPTGTFIEGPKLEAFLDKVPRHVVVVLDEAYTEYLPQEKRYDSIAWVRRY 216
           T+++F+ANPNNPTGT++   ++ +   ++P HV++VLD AY EY+ +      I  V   
Sbjct: 152 TKMVFLANPNNPTGTYVSFDEIRSLRAQLPPHVLLVLDAAYAEYVRRNDYEAGIELVATT 211

Query: 217 PNLLVSRTFSKAFGLAGLRVGFAIAQPELTDLLNRVRQPFNVNTLAQAAAIAALNDKAFL 276
            N +++RTFSK  GLAGLR+G+A     + D+LNR+R PFN++  +  A  AA+ D A  
Sbjct: 212 HNTVMTRTFSKIHGLAGLRIGWAYCPEAVADVLNRIRGPFNLSVPSLLAGAAAIEDSAHE 271

Query: 277 EKSAALNAQGYRRLTEAFDKLGLEYVPSDGNFVLVRVGNDDA-AGNRVNLELLKQGVIVR 335
           E S A N +    L+     LGL+  PS  NF+LV   N+ A   N  +  L ++G+IVR
Sbjct: 272 EMSVAHNEKWLAWLSGEIAALGLKVTPSVANFILVHFPNEGARTANEADRYLKQRGIIVR 331

Query: 336 PVGNYGLPQWLRITIGLPEENEAFIAALERTLAAA 370
            V +YG P  LRITIG  ++N A  AAL   +A +
Sbjct: 332 KVASYGFPDCLRITIGSVDDNRAVAAALTDFMAGS 366


Lambda     K      H
   0.318    0.135    0.385 

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: 385
Number of extensions: 16
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: 370
Length of database: 367
Length adjustment: 30
Effective length of query: 340
Effective length of database: 337
Effective search space:   114580
Effective search space used:   114580
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 (21.7 bits)
S2: 49 (23.5 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