GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Pelobacter propionicus DSM 2379

Align Aromatic-amino-acid transaminase (EC 2.6.1.57) (characterized)
to candidate WP_011735425.1 PPRO_RS07560 histidinol-phosphate transaminase

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



>NCBI__GCF_000015045.1:WP_011735425.1
          Length = 375

 Score =  237 bits (604), Expect = 4e-67
 Identities = 135/365 (36%), Positives = 209/365 (57%), Gaps = 7/365 (1%)

Query: 7   PSYVRAIAPYIAGKPISEVAREFGLDEATIVKLASNENPLGMPESAQRAMAQAASELGR- 65
           P YVR    Y+  +P   + RE+G     + +L +NENPLG P +A R +A    EL   
Sbjct: 8   PDYVRCFQAYVPSRPDHLLMREYGAP--LLYRLNNNENPLGPPPAASREIASFPPELAAV 65

Query: 66  YPDANAFELKAALSERYGVPADWVTLGNGSNDILEIAAHAFVEKGQSIVYAQYSFAVYAL 125
           YP  ++FEL+ AL  R G+  + + +GNGS +++     AF + G +IV A  +FAVY  
Sbjct: 66  YPSGDSFELREALGNRLGISPERILVGNGSCEVISSVIKAFCQPGDNIVTADKTFAVYEW 125

Query: 126 ATQGLGARAIVVPAVKYGHDLDAMLAAVSDDTRLIFVANPNNPTGTFIEGPKLEAFLDKV 185
             +  G +A +VP   +  D   ML  + + T++IFV NPNNPTG++  G  L  FL++V
Sbjct: 126 VAEFSGIQAHLVPLRDHAFDPQGMLDRIDNRTKIIFVCNPNNPTGSYWTGQLLTDFLERV 185

Query: 186 PRHVVVVLDEAYTEYLPQEKRYDSIAWVRRYPNLLVSRTFSKAFGLAGLRVGFAIAQPEL 245
               +VV+DEAY E++  E+  D ++ + R+PNL+V RTFSK + LAGLR G+ +    +
Sbjct: 186 GSERIVVVDEAYREFVEDEEYPDGVSLMERFPNLVVFRTFSKMYALAGLRTGYLVGSDRV 245

Query: 246 TDLLNRVRQPFNVNTLAQAAAIAALNDK-AFLEKSAALNAQGYRRLTEAFDKLGLEYVPS 304
            +++ R    ++VN  AQ AA+AAL+D    +  + AL  +    L  A D LGLE V  
Sbjct: 246 VEVVRRTSVVYSVNVQAQRAALAALSDDGGHIAATRALVRESRAYLRTACDDLGLETVIG 305

Query: 305 DGNFVLVRVGNDDAAGNRVNLELLKQGVIVRPVGNYGLPQWLRITIGLPEENEAFIAALE 364
           +GN++++RV  +D    R    L+K+G++VR +  +  P W+R+T+   E    F  AL 
Sbjct: 306 EGNYLMIRVPINDMLMYR---RLMKRGMMVRSMTGFRYPGWIRVTLKEMEVMTRFAQALG 362

Query: 365 RTLAA 369
             +AA
Sbjct: 363 AEIAA 367


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: 383
Number of extensions: 16
Number of successful extensions: 5
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: 375
Length adjustment: 30
Effective length of query: 340
Effective length of database: 345
Effective search space:   117300
Effective search space used:   117300
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: 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