GapMind for Amino acid biosynthesis

 

Alignments for a candidate for preph-dehydratase in Nitratiruptor tergarcus DSM 16512

Align Bifunctional chorismate mutase/prephenate dehydratase; Chorismate mutase-prephenate dehydratase; P-protein; EC 5.4.99.5; EC 4.2.1.51 (characterized)
to candidate WP_084275314.1 B8779_RS04265 prephenate dehydratase

Query= SwissProt::P27603
         (365 letters)



>NCBI__GCF_900176045.1:WP_084275314.1
          Length = 356

 Score =  237 bits (604), Expect = 4e-67
 Identities = 143/359 (39%), Positives = 206/359 (57%), Gaps = 10/359 (2%)

Query: 5   DQLKALRVRIDSLDERILDLISERARCAQEVARVKTASWPKAEEAVFYRPEREAWVLKHI 64
           ++L+ LR  IDS+D+ IL+L+++R    ++V  +K  +      A  YRPERE  +L  +
Sbjct: 3   EKLQKLREEIDSIDDAILELLNKRMEVVKKVGELKNRT-----NAPIYRPEREIAILNRL 57

Query: 65  MELNKGPLDNEEMARLFREIMSSCLALEQPLRVAYLGPEGTFSQAAALKHFGHSVISKPM 124
            E N+GPL+++ +  +F EI +    LE+P RVAYLGPEG+F+  AA   FG      P 
Sbjct: 58  KEKNRGPLNDKAIEAIFLEIFAVSRNLERPERVAYLGPEGSFTHQAAESRFGAMSEYLPT 117

Query: 125 AAIDEVFREVVAGAVNFGVVPVENSTEGAVNHTLDSFLEHDIVICGEVELRIHHHLLVGE 184
            +I  VF+ V A    +GVVP+ENS +G V  TLD   + D+ I  EV + IHH     E
Sbjct: 118 HSIAAVFKSVEAQRAKYGVVPIENSIDGVVGETLDLLGKSDLKIVAEVYMPIHHSFASLE 177

Query: 185 TTKTDRITRIYSHAQSLAQCRKWLDAHY-PNVERVAVSSNADAAKRVKSEWNSAAIAGDM 243
                +I +IYS   +  QCR +L  H+  +VE++ V S A AA     E  SAAI  ++
Sbjct: 178 -EDLKKIKKIYSKDIAFGQCRNFLQEHFLEDVEQIPVESTAKAAMLAAKEPGSAAICSNI 236

Query: 244 AAQLYGLSKLAEKIEDRPVNSTRFLIIGSQEVPPTGDDKTSIIVSMRNKPGALHELLMPF 303
           AA+LY L  L E IED   N TRF+++ + +   +G DKTSI+  ++++PGAL   L  F
Sbjct: 237 AAKLYNLPILFENIEDVHTNMTRFIVLSNFKNQRSGFDKTSILAKLQDRPGALVRFLEDF 296

Query: 304 HSNGIDLTRIETRPSRSGKWTYVFFIDCMGHHQDPLIKNVLEKIGHEAVALKVLGSYPK 362
            +  I+LT+IE+RP+    + Y F+ID  GH  D   KNV E        +K LGSY K
Sbjct: 297 DAAKINLTKIESRPAEDKDFNYWFYIDFDGHVDD---KNVQEVFAKHKKEIKWLGSYAK 352


Lambda     K      H
   0.319    0.133    0.390 

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: 293
Number of extensions: 10
Number of successful extensions: 3
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: 365
Length of database: 356
Length adjustment: 29
Effective length of query: 336
Effective length of database: 327
Effective search space:   109872
Effective search space used:   109872
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: 49 (23.5 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