Align Ornithine aminotransferase; Orn-AT; Lysine aminotransferase; Lys-AT; EC 2.6.1.13; EC 2.6.1.36 (characterized)
to candidate WP_076948621.1 C1M55_RS28045 4-aminobutyrate--2-oxoglutarate transaminase
Query= SwissProt::Q5JEW1 (445 letters) >NCBI__GCF_002893965.1:WP_076948621.1 Length = 457 Score = 256 bits (653), Expect = 1e-72 Identities = 163/445 (36%), Positives = 229/445 (51%), Gaps = 14/445 (3%) Query: 3 VRPNVKELPGPKAKEVIERNFKYLAMTTQDPENLPIVIERGEGIRVYDVDGNVFYDFASG 62 +R V E+PGP ++ + +R L ++ V G G+ V DVD N F DF SG Sbjct: 20 IRRLVTEVPGPNSRALAKRRSAALPAGLTSGSSI-YVAAAGGGV-VVDVDDNSFIDFGSG 77 Query: 63 VGVINVGHSHPRVVEAIKKQAEKFTHYSLTDFFYENAIILAEKLIELAPGDIERKVVYGN 122 + V VG+S PRVVE +Q +FTH YE + + E L L PGD E++ N Sbjct: 78 IAVTTVGNSAPRVVERTTRQLGQFTHTCFLANPYEGYLEVCEALNRLTPGDHEKRTALFN 137 Query: 123 SGAEANEAAMKLVKYGTGRKQFLAFYHAFHGRTQAVLSLTASKWVQQDGFFPTMPGVTHI 182 +G+EA E A+K + TGR + F HAFHGRT +++TA + F P P V + Sbjct: 138 TGSEALENAVKYARAATGRPAVVVFDHAFHGRTLMTMTMTAKNQPYKATFGPFAPEVYRV 197 Query: 183 PYPNPYRNTWGIDGYEEPDELTNRVLDFIEEYVFRHVPPHEIGAIFFEPIQGEGGYVVPP 242 P PYR G P+ + + + + A+ EPIQGEGG++VP Sbjct: 198 PMAYPYRWPSG------PENAADEAFAQFRLAIDTQIGAESVAAVVVEPIQGEGGFIVPA 251 Query: 243 KGFFKALKKFADEYGILLADDEVQMGIGRTGKFWAIEHFGVEPDLIQFGKAIGGGLPLAG 302 GF K + +F E GIL+ DEVQ GI RTG ++A E PD+I K + GG+PLA Sbjct: 252 PGFLKRISEFCRERGILVVADEVQTGIARTGSWFASESEDFVPDIITTAKGLAGGMPLAA 311 Query: 303 VIHRADI-TFDKPGRHATTFGGNPVAIAAGIEVVEIV--KELLPHVQEVGDYLHKYLEEF 359 V RAD+ PG T+ GNPVA A + V E + + LL +++GD L L E Sbjct: 312 VTGRADVMDAAHPGGIGGTYSGNPVACEAALAVFETIEMEGLLDRAKDIGDILTTGLSEI 371 Query: 360 KEKYEVIGDARGLGLAQAVEIVKSKETKEKYPELRDRIVKESAKRGLVLLGCG--DNSIR 417 ++IGD RG G A+E+V E K E +IV + GL+LL G N +R Sbjct: 372 ASDTDIIGDIRGRGAMIAIELVHD-EDKAPNREAVAQIVSYAHAHGLLLLTAGTYGNVVR 430 Query: 418 FIPPLIVTKEEIDVAMEIFEEALKA 442 F+PPL ++ E + + I +A+ A Sbjct: 431 FLPPLSISDELLTEGLGILRDAVAA 455 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: 512 Number of extensions: 26 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: 457 Length adjustment: 33 Effective length of query: 412 Effective length of database: 424 Effective search space: 174688 Effective search space used: 174688 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 24 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:
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