Align D-lysine oxidase (EC 1.4.3.3) (characterized)
to candidate BPHYT_RS10270 BPHYT_RS10270 D-amino acid dehydrogenase
Query= metacyc::G1G01-3833-MONOMER (414 letters) >lcl|FitnessBrowser__BFirm:BPHYT_RS10270 BPHYT_RS10270 D-amino acid dehydrogenase Length = 413 Score = 439 bits (1129), Expect = e-128 Identities = 230/414 (55%), Positives = 271/414 (65%), Gaps = 3/414 (0%) Query: 1 MHCQTLVLGAGIVGVSTALHLQARGRQVILIDRDEPGSGTSHGNAGLIERSSVIPYAFPR 60 M +VLGAGIVGVS+ALHLQ RGR+V L+DR PG TS GNAGLIE SSV+PYAFPR Sbjct: 1 MDFDVIVLGAGIVGVSSALHLQDRGRRVALVDRRGPGEETSFGNAGLIESSSVVPYAFPR 60 Query: 61 QLSALLRYGLNRQPDVRYSLAHLPKAAPWLWRYWRQSAPGRLAGAAADMLPLVQRCVDEH 120 L LLRY NR D+ + LP A WL R+W +S+P RL AA DMLPL++ V EH Sbjct: 61 NLGTLLRYARNRSTDLYWDYRALPSFAGWLARFWWESSPERLMAAAHDMLPLMRHSVAEH 120 Query: 121 DALIAAAGLEGLVQAKGWIEVFRDPALFEQAKTDAK-GLSRYGLRFEILECGQLQAREHQ 179 D LIA AGLE L KGWIE FR PA F + A+ + YGLR L+ L ARE Sbjct: 121 DVLIARAGLEQLASDKGWIEAFRTPAEFSRQSAAAEVTANTYGLRVTTLDAAALAAREPG 180 Query: 180 LDATVVGGIHWLDPKTVNNPGALTRGYAALFLQRGGQFVHGDARSLRQANGQWRVESRRG 239 + G +HW DPK++ NPGALT+GYA LF + GG + GDA +L+ G W V++ G Sbjct: 181 VAEGFCGALHWQDPKSIVNPGALTQGYARLFEESGGALLTGDATTLKAEGGAWTVQTSSG 240 Query: 240 PITADEVVACLGPQSADLFSGLGYQIPLAIKRGYHMHYSTRDGAQLEHSICDTQGGYVLA 299 I+A EVV LGP S +F+ LGY+IPL KRGYHMHY L + D+Q GYV+A Sbjct: 241 RISAKEVVVALGPWSDRVFAPLGYRIPLRAKRGYHMHYQPTQ-PMLSTPLVDSQQGYVVA 299 Query: 300 PMARGVRLTTGIEFDAASAPGNQIQLGRCEALARKLFPALGDRLDDTPWLGRRPCLPDMR 359 PM +RLTTG+E A +QL R E AR F LG RLD+ PWLG RPC PDMR Sbjct: 300 PMQGRLRLTTGVEIARREAAPTGVQLERAERTARPTF-GLGARLDEHPWLGLRPCTPDMR 358 Query: 360 PVIGPAPRHPGLWFNFGHAHHGLTLGPVCGRLLAELLTGEPPFTDPAPYSATRF 413 PVIGPAPRH GLWF FGH HHGLTLGPV GRLLAE++TG PF D P+ RF Sbjct: 359 PVIGPAPRHRGLWFAFGHNHHGLTLGPVTGRLLAEMMTGAEPFVDARPFRPERF 412 Lambda K H 0.322 0.140 0.447 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: 574 Number of extensions: 22 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: 414 Length of database: 413 Length adjustment: 31 Effective length of query: 383 Effective length of database: 382 Effective search space: 146306 Effective search space used: 146306 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 Sep 17 2021. The underlying query database was built on Sep 17 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 preprint on GapMind for carbon sources, or view the source code.
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