Align Succinylornithine transaminase; EC 2.6.1.81; Succinylornithine aminotransferase (uncharacterized)
to candidate Ga0059261_3205 Ga0059261_3205 transaminase, acetylornithine/succinylornithine family
Query= curated2:B7USC9 (406 letters) >lcl|FitnessBrowser__Korea:Ga0059261_3205 Ga0059261_3205 transaminase, acetylornithine/succinylornithine family Length = 398 Score = 327 bits (838), Expect = 4e-94 Identities = 171/393 (43%), Positives = 238/393 (60%), Gaps = 10/393 (2%) Query: 14 MIPVYAPAPFIPVRGEGSRLWDQQGKEYIDFSGGIAVNALGHAHPELREALNEQASKFWH 73 ++PVY PVRGEG L ++G+ Y+DF+ GIAVNALGH HP+ +A+ EQA+ H Sbjct: 6 LMPVYPRCEVRPVRGEGCYLIGERGERYLDFAAGIAVNALGHGHPQFTKAIAEQAATLMH 65 Query: 74 TGNGYTNEPVLRLAKKLIDATFADRVFFCNSGAEANEAALKLARKFAHDRYGSHKSGIVA 133 N Y + LA++++D +FAD VFF NSG EA E A+K AR++ + + ++ Sbjct: 66 VSNLYGSPQGEALAQRIVDNSFADTVFFTNSGVEAIECAIKTARRYHYVNGNPQRHKLIT 125 Query: 134 FKNAFHGRTLFTVSAGGQPAYSQDFAPLPPDIRHAAYNDINSASALIDDATCAVIVEPIQ 193 FKNAFHGR++ +SA QP F PL P + +ND+ A A IDD T +VE +Q Sbjct: 126 FKNAFHGRSIGAISATDQPKMRDGFEPLLPGFDYVKFNDLEGAIAKIDDETAGFLVETVQ 185 Query: 194 GEGGVVPASNAFLQGLRELCDRHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLTTAKA 253 GEGG+ + F+QGLR+ CD H LLI DE+Q G GRTG+++AY HYG+TPD+LT AK Sbjct: 186 GEGGMTAGTVEFIQGLRKACDEHGLLLILDEIQCGYGRTGKMWAYEHYGITPDILTAAKG 245 Query: 254 LGGGFPVGALLATKECASVMTVGTHGTTYGGNPLASAVAGKVLDLINTPEMLNGVKQRHD 313 +G GFP+GA LAT+E A MT GTHG+TYGGNPLA A VLD++ P V++ Sbjct: 246 IGNGFPLGACLATEEAAKGMTFGTHGSTYGGNPLAMAAGQAVLDVMLEPGFFEHVEK--- 302 Query: 314 WFVERLNS-----INHHYSLFSEVRGLGLLIGCVLNADYAGQAKQISQEAVKAGVMVLIA 368 ERL + I +H LF E+RG GL++G L + A ++ G++ + A Sbjct: 303 -MGERLRAGFEQLIPNHDHLFDEIRGKGLMLGIKLK-EPAVSRDFVAHLRENHGLLTVAA 360 Query: 369 GGNVVRFAPALNVSEEEVTTGLDRFSAACEHFV 401 G NV R P L + E + +++ SA +V Sbjct: 361 GENVFRVLPPLVIEESHIAECIEKLSAGARSYV 393 Lambda K H 0.319 0.135 0.408 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: 479 Number of extensions: 24 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: 406 Length of database: 398 Length adjustment: 31 Effective length of query: 375 Effective length of database: 367 Effective search space: 137625 Effective search space used: 137625 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 (21.8 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