GapMind for Amino acid biosynthesis

 

Alignments for a candidate for preph-dehydratase in Thermodesulforhabdus norvegica DSM 9990

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_093393469.1 BM091_RS03430 prephenate dehydratase

Query= SwissProt::P27603
         (365 letters)



>NCBI__GCF_900114975.1:WP_093393469.1
          Length = 393

 Score =  249 bits (635), Expect = 1e-70
 Identities = 135/358 (37%), Positives = 212/358 (59%), Gaps = 7/358 (1%)

Query: 7   LKALRVRIDSLDERILDLISERARCAQEVARVKTASWPKAEEAVFYRPEREAWVLKHIME 66
           L  LR+ ID +D+ ++  ++ R R + EV RVK     +A+    + P+RE  +LK ++ 
Sbjct: 13  LDDLRIEIDEVDKELVRWLARRMRLSYEVGRVK-----RAQGLPLFDPDREEAILKKLVT 67

Query: 67  LNKGPLDNEEMAR-LFREIMSSCLALEQPLRVAYLGPEGTFSQAAALKHFGHSVISKPMA 125
           LN  PL    + R ++REI+++  +L+ P++VA+LGP  T+S  AAL  FGH V   P +
Sbjct: 68  LNTEPLLTPPILRSIYREILAASRSLQYPVKVAFLGPLWTYSHIAALFVFGHDVEYNPCS 127

Query: 126 AIDEVFREVVAGAVNFGVVPVENSTEGAVNHTLDSFLEHDIVICGEVELRIHHHLLVGET 185
           +++EVF  V     +  VVPVENS EG++  T+D    +D+ I  E  + + +HL  G  
Sbjct: 128 SMEEVFESVARNRYDIAVVPVENSVEGSIGITMDLMYRYDLYIVRECYVAMEYHL-AGNV 186

Query: 186 TKTDRITRIYSHAQSLAQCRKWLDAHYPNVERVAVSSNADAAKRVKSEWNSAAIAGDMAA 245
                I  +Y+H ++ +QCR+WL  H  +V  V  SS A AA+  +     AA+    AA
Sbjct: 187 EDLKEIREVYAHPRAFSQCRRWLAEHLSDVALVECSSTAQAAELCREVRGRAALCNLYAA 246

Query: 246 QLYGLSKLAEKIEDRPVNSTRFLIIGSQEVPPTGDDKTSIIVSMRNKPGALHELLMPFHS 305
             +GL+ +AE I D P + TRF+ +  ++  P+GDDKTSII  + + PGAL+  L P   
Sbjct: 247 HHFGLNVVAEHISDYPDSVTRFIALSREKTSPSGDDKTSIIFGVSHAPGALYRALEPCVR 306

Query: 306 NGIDLTRIETRPSRSGKWTYVFFIDCMGHHQDPLIKNVLEKIGHEAVALKVLGSYPKA 363
           +G++LTRIE+RP+R    +Y+FF+D  GH  DP ++  L ++      +K+LGSYP+A
Sbjct: 307 HGVNLTRIESRPARVPLKSYLFFVDLEGHENDPSVRAALSEMEDALPFVKILGSYPRA 364


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: 329
Number of extensions: 8
Number of successful extensions: 4
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: 393
Length adjustment: 30
Effective length of query: 335
Effective length of database: 363
Effective search space:   121605
Effective search space used:   121605
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