GapMind for Amino acid biosynthesis

 

Alignments for a candidate for preph-dehydratase in Desulfatibacillum aliphaticivorans DSM 15576

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_028315507.1 G491_RS0117450 prephenate dehydratase

Query= SwissProt::P27603
         (365 letters)



>NCBI__GCF_000429905.1:WP_028315507.1
          Length = 365

 Score =  290 bits (742), Expect = 4e-83
 Identities = 155/356 (43%), Positives = 224/356 (62%), Gaps = 6/356 (1%)

Query: 6   QLKALRVRIDSLDERILDLISERARCAQEVARVKTASWPKAEEAVFYRPEREAWVLKHIM 65
           +L+ LR  I+  D++IL L++ER   AQ++  +K     K    V +  ER   VL  + 
Sbjct: 11  ELEPLRQAINETDQKILALVNERLDIAQKIGAIKQG---KGLPVVDFSRERA--VLNKLQ 65

Query: 66  ELNKGPLDNEEMARLFREIMSSCLALEQPLRVAYLGPEGTFSQAAALKHFGHSVISKPMA 125
           ELN+GP+ +E +  L+ EI+++   ++QPL V YLGP+ TF+  AA+KHFG S    P+A
Sbjct: 66  ELNEGPMPDETLLLLYTEIIAASRRIQQPLEVGYLGPKATFTHMAAMKHFGRSTNFTPLA 125

Query: 126 AIDEVFREVVAGAVNFGVVPVENSTEGAVNHTLDSFLEHDIVICGEVELRIHHHLLVGET 185
            I +VF EV      FGVVPVENS EGAVN TLD F E D+ ICGE+ L I H LL  E 
Sbjct: 126 TISDVFEEVDKRRRPFGVVPVENSMEGAVNLTLDLFQESDVRICGEIYLPIRHDLLSAED 185

Query: 186 TKTDRITRIYSHAQSLAQCRKWLDAHYPNVERVAVSSNADAAKRVKSEWNSAAIAGDMAA 245
           +  D+I  ++SH Q++AQCRKWL  + P + +   SS ++AA+   +    AAIA   AA
Sbjct: 186 S-LDQIMVVFSHPQAIAQCRKWLGKNLPGILQNQCSSTSEAARMAVNTPGGAAIASSEAA 244

Query: 246 QLYGLSKLAEKIEDRPVNSTRFLIIGSQEVPPTGDDKTSIIVSMRNKPGALHELLMPFHS 305
             Y L+ LA+ I+D   N TRFL+IG  +V PTG DKTS++ ++ + PGALH +L P   
Sbjct: 245 ITYELNTLADNIQDSTTNITRFLVIGRDKVQPTGRDKTSLLFAIPHIPGALHSVLQPISE 304

Query: 306 NGIDLTRIETRPSRSGKWTYVFFIDCMGHHQDPLIKNVLEKIGHEAVALKVLGSYP 361
            G+++ ++E+RPS+S  W Y+FF+D  GH +D  +K V++K+      +K +GSYP
Sbjct: 305 EGLNMVKLESRPSKSASWHYLFFVDLEGHMKDEPVKKVVDKMRSLCSFVKWMGSYP 360


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: 338
Number of extensions: 12
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: 365
Length of database: 365
Length adjustment: 30
Effective length of query: 335
Effective length of database: 335
Effective search space:   112225
Effective search space used:   112225
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 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