Align Ornithine aminotransferase; Orn-AT; Lysine aminotransferase; Lys-AT; EC 2.6.1.13; EC 2.6.1.36 (characterized)
to candidate BPHYT_RS10155 BPHYT_RS10155 2,2-dialkylglycine decarboxylase
Query= SwissProt::Q5JEW1 (445 letters) >lcl|FitnessBrowser__BFirm:BPHYT_RS10155 BPHYT_RS10155 2,2-dialkylglycine decarboxylase Length = 433 Score = 216 bits (550), Expect = 1e-60 Identities = 144/417 (34%), Positives = 218/417 (52%), Gaps = 18/417 (4%) Query: 37 PIVIERGEGIRVYDVDGNVFYDFASGVGVINVGHSHPRVVEAIKKQAEKFTHYSLTDFFY 96 P++IER +G VYD DG DF SG +GHSHP +V I + A K H + Sbjct: 26 PMIIERAQGSFVYDADGRAILDFTSGQMSAVLGHSHPEIVSVINEYAGKLDHL-FSGMLS 84 Query: 97 ENAIILAEKLIELAPGDIERKVVYGNSGAEANEAAMKLVKYGTGRKQFLAFYHAFHGRTQ 156 + LA +L E+ P ++R ++ ++GAE+NEAA+++ K TG+ + + F ++HG T Sbjct: 85 RPVVDLATRLAEITPDGLDRALLL-STGAESNEAAIRMAKLVTGKYEIVGFAQSWHGMTA 143 Query: 157 AVLSLTASKWVQQDGFFPTMPGVTHIPYPNPYRNTWGIDGYEEPDELTNRVLDFIEEYVF 216 A S T S + G P G IP P YR + G + D L LD+ + + Sbjct: 144 AAASATYS--AGRKGVGPAAVGSFAIPAPFLYRPRFERHG--DYDYLAE--LDYAFDLID 197 Query: 217 RHVPPHEIGAIFFEPIQGEGGYVVPPKGFFKALKKFADEYGILLADDEVQMGIGRTGKFW 276 R + + A EPI GG + P+G+ ALK+ +E G+LL DE Q G+GRTG + Sbjct: 198 RQSSGN-LAAFIAEPILSSGGIIELPEGYMTALKRKCEERGMLLILDEAQTGVGRTGTMF 256 Query: 277 AIEHFGVEPDLIQFGKAIGGGLPLAGVIHRADI---TFDKPGRHATTFGGNPVAIAAGIE 333 A + GV PD++ K +G GLPLA V+ A I + TT +P+ A G+ Sbjct: 257 ACQRDGVTPDILTLSKTLGAGLPLAAVVTSAQIEERAHELGYLFYTTHVSDPLPAAVGLR 316 Query: 334 VVEIVKE--LLPHVQEVGDYLHKYLEEFKEKYEVIGDARGLGLAQAVEIVKSKETKEKYP 391 V+E+V+ L+ +G L + L + E+++ IGD RG GL +EIVK + TKE Sbjct: 317 VLEVVERDGLVARANLMGARLKRGLLDLMERFDCIGDIRGRGLLLGMEIVKDRRTKEPAD 376 Query: 392 ELRDRIVKESAKRGL----VLLGCGDNSIRFIPPLIVTKEEIDVAMEIFEEALKAAL 444 L +I +E GL V L R PPL V ++EID+ +++ +A++ +L Sbjct: 377 GLGAKITRECMNLGLSMNIVQLPGMGGVFRIAPPLTVHEDEIDLGLDLLGQAIERSL 433 Lambda K H 0.320 0.141 0.418 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: 486 Number of extensions: 28 Number of successful extensions: 5 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: 445 Length of database: 433 Length adjustment: 32 Effective length of query: 413 Effective length of database: 401 Effective search space: 165613 Effective search space used: 165613 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 (21.7 bits) S2: 51 (24.3 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