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 Dsui_1940 Dsui_1940 chorismate mutase, clade 2
Query= SwissProt::P27603 (365 letters) >FitnessBrowser__PS:Dsui_1940 Length = 374 Score = 386 bits (991), Expect = e-112 Identities = 192/360 (53%), Positives = 254/360 (70%), Gaps = 6/360 (1%) Query: 7 LKALRVRIDSLDERILDLISERARCAQEVARVKTASWPKAEEAVFYRPEREAWVLKHIME 66 L +R+ ID++D ++LDL++ RARCAQ+V +K + YRPEREA VL+ I + Sbjct: 18 LSVVRMDIDAIDAQLLDLLNRRARCAQQVGEIKARH---GDAGFIYRPEREAQVLRRIQD 74 Query: 67 LNKGPLDNEEMARLFREIMSSCLALEQPLRVAYLGPEGTFSQAAALKHFGHSVISKPMAA 126 +N+GPL +E + FRE+MS+CL+LEQPL +A+LGP GTFS++A+ KHFGH+ P A+ Sbjct: 75 MNQGPLSSESVTWFFREVMSACLSLEQPLGIAFLGPLGTFSESASTKHFGHAARLLPQAS 134 Query: 127 IDEVFREVVAGAVNFGVVPVENSTEGAVNHTLDSFLEHDIVICGEVELRIHHHLLVGETT 186 ID+VFREV AG N+GV PVENSTEGAV TLD L + ICGEV LRIH HLL + Sbjct: 135 IDDVFREVEAGHANYGVAPVENSTEGAVGRTLDLLLGTSLKICGEVVLRIHQHLLT-KAP 193 Query: 187 KTDRITRIYSHAQSLAQCRKWLDAHYPNVERVAVSSNADAAKRVKSEWNSAAIAGDMAAQ 246 DR+T++YSHAQSLAQC +WL+ H PNV R++V SNA AA+ E +AAIAG+ AA Sbjct: 194 SLDRVTKVYSHAQSLAQCHEWLNRHLPNVPRISVGSNAQAAQMAAQEEGAAAIAGEAAAD 253 Query: 247 LYGLSKLAEKIEDRPVNSTRFLIIGSQEVPPT--GDDKTSIIVSMRNKPGALHELLMPFH 304 Y L +LAE IED P N+TRF+++G + P+ G DKTS+I+S+ N GALH LL+PF Sbjct: 254 RYDLPRLAESIEDEPNNTTRFVVLGRHDAGPSTAGKDKTSLIMSIPNNTGALHTLLVPFA 313 Query: 305 SNGIDLTRIETRPSRSGKWTYVFFIDCMGHHQDPLIKNVLEKIGHEAVALKVLGSYPKAV 364 G+ LTR+E+RP+R W YVFF+D GH +P +K L+++ A LKVLGSYP AV Sbjct: 314 DAGVSLTRLESRPARHTLWEYVFFVDVDGHRDEPRVKAALDELARRAAYLKVLGSYPVAV 373 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: 375 Number of extensions: 16 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: 374 Length adjustment: 30 Effective length of query: 335 Effective length of database: 344 Effective search space: 115240 Effective search space used: 115240 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)
Align candidate Dsui_1940 Dsui_1940 (chorismate mutase, clade 2)
to HMM TIGR01807 (pheA: chorismate mutase (EC 5.4.99.5))
# hmmsearch :: search profile(s) against a sequence database # HMMER 3.3.1 (Jul 2020); http://hmmer.org/ # Copyright (C) 2020 Howard Hughes Medical Institute. # Freely distributed under the BSD open source license. # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # query HMM file: ../tmp/path.aa/TIGR01807.hmm # target sequence database: /tmp/gapView.1428630.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR01807 [M=76] Accession: TIGR01807 Description: CM_P2: chorismate mutase Scores for complete sequences (score includes all domains): --- full sequence --- --- best 1 domain --- -#dom- E-value score bias E-value score bias exp N Sequence Description ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 1.5e-34 104.4 0.1 2.1e-33 100.8 0.1 2.3 2 FitnessBrowser__PS:Dsui_1940 Domain annotation for each sequence (and alignments): >> FitnessBrowser__PS:Dsui_1940 # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 100.8 0.1 2.1e-33 2.1e-33 2 76 .] 19 93 .. 18 93 .. 0.97 2 ? 0.9 0.0 0.03 0.03 62 75 .. 129 142 .. 120 143 .. 0.89 Alignments for each domain: == domain 1 score: 100.8 bits; conditional E-value: 2.1e-33 TIGR01807 2 kelRnkiDaiDdrildLlseRaklakavgelKkksaseaviYRPeREaavlrrlkelnkGpLdqeavarifrEim 76 +R iDaiD+++ldLl+ Ra++a++vge+K + + ++iYRPeREa+vlrr++++n+GpL +e+v frE+m FitnessBrowser__PS:Dsui_1940 19 SVVRMDIDAIDAQLLDLLNRRARCAQQVGEIKARHGDAGFIYRPEREAQVLRRIQDMNQGPLSSESVTWFFREVM 93 56899*********************************************************************9 PP == domain 2 score: 0.9 bits; conditional E-value: 0.03 TIGR01807 62 pLdqeavarifrEi 75 +L+q +++ +frE+ FitnessBrowser__PS:Dsui_1940 129 LLPQASIDDVFREV 142 799**********8 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (76 nodes) Target sequences: 1 (374 residues searched) Passed MSV filter: 1 (1); expected 0.0 (0.02) Passed bias filter: 1 (1); expected 0.0 (0.02) Passed Vit filter: 1 (1); expected 0.0 (0.001) Passed Fwd filter: 1 (1); expected 0.0 (1e-05) Initial search space (Z): 1 [actual number of targets] Domain search space (domZ): 1 [number of targets reported over threshold] # CPU time: 0.00u 0.00s 00:00:00.00 Elapsed: 00:00:00.00 # Mc/sec: 16.94 // [ok]
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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:
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