Align fused chorismate mutase/prephenate dehydrogenase (EC 5.4.99.5; EC 1.3.1.12) (characterized)
to candidate WP_035241586.1 Q366_RS17620 bifunctional chorismate mutase/prephenate dehydrogenase
Query= ecocyc::CHORISMUTPREPHENDEHYDROG-MONOMER (373 letters) >NCBI__GCF_000745975.1:WP_035241586.1 Length = 380 Score = 323 bits (828), Expect = 5e-93 Identities = 161/365 (44%), Positives = 236/365 (64%), Gaps = 1/365 (0%) Query: 4 ELTALRDQIDEVDKALLNLLAKRLELVAEVGEVKSRFGLPIYVPEREASMLASRRAEAEA 63 ++ +RD+ID +D +++LL+KR E V ++ VK +PIY P RE +++ R +A Sbjct: 11 QIKPIRDEIDAIDARIISLLSKRREQVEKIVAVKKEHKVPIYHPAREEDVISRLRGKASD 70 Query: 64 LGVPPDLIEDVLRRVMRESYSSENDKGFKTLCPSLRPVVIVGGGGQMGRLFEKMLTLSGY 123 + V PDL+E++ R +M +S S+ +L +++VGG G+MGRLF + T +GY Sbjct: 71 MDVDPDLVENLYRTIMHQSRKSQTRVSKTSLIRPQARILVVGGAGEMGRLFVRFFTDTGY 130 Query: 124 QVRILEQHDWDRAADIVADAGMVIVSVPIHVTEQVIGKLPPLPK-DCILVDLASVKNGPL 182 V IL++ DWDRA + +A +VIV VPI+VT +VI L PL + D +L DL SVK PL Sbjct: 131 PVDILDKDDWDRAQALCKNADLVIVCVPINVTVKVIDALAPLMRPDAVLTDLTSVKTLPL 190 Query: 183 QAMLVAHDGPVLGLHPMFGPDSGSLAKQVVVWCDGRKPEAYQWFLEQIQVWGARLHRISA 242 +AM AH GPVLGLHP+FGP + +L KQ++ C G+K +A QW ++Q+ WGA + SA Sbjct: 191 EAMCRAHTGPVLGLHPLFGPTTNNLDKQIIAACSGQKDDACQWVIDQLVAWGAVVVETSA 250 Query: 243 VEHDQNMAFIQALRHFATFAYGLHLAEENVQLEQLLALSSPIYRLELAMVGRLFAQDPQL 302 EHDQ M +QALRHFATF++G L + + +++ L SSPIYRLEL MVGRLFAQDP L Sbjct: 251 REHDQVMEIVQALRHFATFSFGSFLYRQGIPIKRTLEFSSPIYRLELGMVGRLFAQDPDL 310 Query: 303 YADIIMSSERNLALIKRYYKRFGEAIELLEQGDKQAFIDSFRKVEHWFGDYAQRFQSESR 362 YA+II ++ L+K + + + +++LE GDK AFI F ++ WFG + + ES Sbjct: 311 YAEIIFATPERRQLLKTFVQSLTQFLDMLESGDKDAFIKEFNQIAEWFGPFGNQALREST 370 Query: 363 VLLRQ 367 + + Sbjct: 371 YFINK 375 Lambda K H 0.322 0.138 0.404 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: 377 Number of extensions: 14 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: 373 Length of database: 380 Length adjustment: 30 Effective length of query: 343 Effective length of database: 350 Effective search space: 120050 Effective search space used: 120050 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 (21.9 bits) S2: 50 (23.9 bits)
Align candidate WP_035241586.1 Q366_RS17620 (bifunctional chorismate mutase/prephenate dehydrogenase)
to HMM PF01817 (CM_2)
# 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/PF01817.25.hmm # target sequence database: /tmp/gapView.3748114.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: CM_2 [M=79] Accession: PF01817.25 Description: Chorismate mutase type II 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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 1.1e-27 82.5 2.5 2.9e-27 81.2 2.5 1.7 1 NCBI__GCF_000745975.1:WP_035241586.1 Domain annotation for each sequence (and alignments): >> NCBI__GCF_000745975.1:WP_035241586.1 # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 81.2 2.5 2.9e-27 2.9e-27 1 78 [. 16 93 .. 16 94 .. 0.99 Alignments for each domain: == domain 1 score: 81.2 bits; conditional E-value: 2.9e-27 CM_2 1 RkeIdeiDrelleLlaeRmelakeiaeyKkenglpvldpeReeevlerlregaeelgldpeavekifreiisesr 75 R+eId+iD++++ Ll++R e +++i ++Kke+++p++ p+Ree+v++rlr +a+++++dp++ve+++r+i++ sr NCBI__GCF_000745975.1:WP_035241586.1 16 RDEIDAIDARIISLLSKRREQVEKIVAVKKEHKVPIYHPAREEDVISRLRGKASDMDVDPDLVENLYRTIMHQSR 90 99************************************************************************* PP CM_2 76 alQ 78 + Q NCBI__GCF_000745975.1:WP_035241586.1 91 KSQ 93 *99 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (79 nodes) Target sequences: 1 (380 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: 14.85 // [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