Align fused chorismate mutase/prephenate dehydrogenase (EC 5.4.99.5; EC 1.3.1.12) (characterized)
to candidate BWI76_RS21475 BWI76_RS21475 bifunctional chorismate mutase/prephenate dehydrogenase
Query= ecocyc::CHORISMUTPREPHENDEHYDROG-MONOMER (373 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS21475 BWI76_RS21475 bifunctional chorismate mutase/prephenate dehydrogenase Length = 373 Score = 670 bits (1729), Expect = 0.0 Identities = 340/373 (91%), Positives = 353/373 (94%) Query: 1 MVAELTALRDQIDEVDKALLNLLAKRLELVAEVGEVKSRFGLPIYVPEREASMLASRRAE 60 MVAELTALRDQIDEVDKALL LLAKRLELVA+VGEVKS +GLPIYVPERE++MLASRR E Sbjct: 1 MVAELTALRDQIDEVDKALLELLAKRLELVAQVGEVKSHYGLPIYVPERESAMLASRREE 60 Query: 61 AEALGVPPDLIEDVLRRVMRESYSSENDKGFKTLCPSLRPVVIVGGGGQMGRLFEKMLTL 120 A ALGVPPDLIEDVLRRVMRESYSSENDKGFKTL P+LRPVVIVGGGGQMGRLFEKMLTL Sbjct: 61 AAALGVPPDLIEDVLRRVMRESYSSENDKGFKTLYPNLRPVVIVGGGGQMGRLFEKMLTL 120 Query: 121 SGYQVRILEQHDWDRAADIVADAGMVIVSVPIHVTEQVIGKLPPLPKDCILVDLASVKNG 180 SGYQVRILE+ DW RA +IVADAGMVIVSVPIH+T I +LPPLP DCILVDLASVK Sbjct: 121 SGYQVRILEKDDWSRADEIVADAGMVIVSVPIHITAATIAQLPPLPADCILVDLASVKAE 180 Query: 181 PLQAMLVAHDGPVLGLHPMFGPDSGSLAKQVVVWCDGRKPEAYQWFLEQIQVWGARLHRI 240 PLQAML AH GPVLGLHPMFGPDSGSLAKQVVV+CDGR+PEAYQWFLEQIQVWGARLHRI Sbjct: 181 PLQAMLAAHKGPVLGLHPMFGPDSGSLAKQVVVYCDGRQPEAYQWFLEQIQVWGARLHRI 240 Query: 241 SAVEHDQNMAFIQALRHFATFAYGLHLAEENVQLEQLLALSSPIYRLELAMVGRLFAQDP 300 SAVEHDQNMAFIQALRHFATFAYGLHLAEENV+LEQLLALSSPIYRLELAMVGRLFAQDP Sbjct: 241 SAVEHDQNMAFIQALRHFATFAYGLHLAEENVRLEQLLALSSPIYRLELAMVGRLFAQDP 300 Query: 301 QLYADIIMSSERNLALIKRYYKRFGEAIELLEQGDKQAFIDSFRKVEHWFGDYAQRFQSE 360 QLYADIIMSSE NLALIKRYY+RFGEAI LLEQGDKQAFIDSFRKVEHWFGDYAQRFQSE Sbjct: 301 QLYADIIMSSENNLALIKRYYQRFGEAIGLLEQGDKQAFIDSFRKVEHWFGDYAQRFQSE 360 Query: 361 SRVLLRQANDNRQ 373 SR LLRQANDNRQ Sbjct: 361 SRTLLRQANDNRQ 373 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: 545 Number of extensions: 13 Number of successful extensions: 1 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: 373 Length adjustment: 30 Effective length of query: 343 Effective length of database: 343 Effective search space: 117649 Effective search space used: 117649 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)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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