Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate AO356_17010 AO356_17010 acetylornithine aminotransferase
Query= reanno::Koxy:BWI76_RS11670 (406 letters) >lcl|FitnessBrowser__pseudo5_N2C3_1:AO356_17010 AO356_17010 acetylornithine aminotransferase Length = 391 Score = 275 bits (704), Expect = 1e-78 Identities = 157/377 (41%), Positives = 218/377 (57%), Gaps = 9/377 (2%) Query: 14 MMPVYAPAAFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPRLVKALTEQAGKFWH 73 +M Y P A G G+RLWDQ G+EY+D G+AV +GH+HPRLV A++EQAG H Sbjct: 6 LMTTYQPLALNFTHGLGTRLWDQDGREYLDAVAGVAVTNVGHSHPRLVAAISEQAGLLLH 65 Query: 74 TGNGYTNEPVLRLAKQLIDATFADRVFFCNSGAEANEAALKLARKYAHDRFGSEKSGIVA 133 T N Y+ + RLA++L + +R FF NSGAEANE ALKLAR Y + G E+ +V Sbjct: 66 TSNLYSIDWQQRLAQKLTQLSGMERAFFNNSGAEANETALKLARLYGWHK-GIEQPLVVV 124 Query: 134 FKNAFHGRTLFTVSAGGQPAYSQDFAPLPPQIQHAIYNDLDSAKALID---DNTCAVIVE 190 NAFHGRTL T+SA P+ + LP + DL + + + + AV+VE Sbjct: 125 MDNAFHGRTLGTMSASDGPSVRLGYNRLPGDFIKVPFGDLAALEQIQQAHAERIVAVLVE 184 Query: 191 PMQGEGGVVPADADFLRGLRELCDAHNALLIFDEVQTGVGRTGELYAYMHYGVTPDLLST 250 P+QGE GV A +L+ LR+LC LL+ DE+QTG+GRTG+ +A+ H G+ PD+++ Sbjct: 185 PIQGESGVQLAPPGYLKALRQLCSRRAWLLMLDEIQTGIGRTGQWFAFQHEGIVPDVMTL 244 Query: 251 AKALGGGFPIGALLASERCASVMTVGTHGTTYGGNPLACAVAGEVFATINTREVLNGVKQ 310 AK LG G PIGA LA + A + T G+HG+T+GGNPLAC V V I + ++ + Sbjct: 245 AKGLGNGVPIGACLARGKAAELFTPGSHGSTFGGNPLACRVGCTVLDIIEEQALVGNARH 304 Query: 311 RHQWFCERLNAINARYGLFKEIRGLGLLIGCVLKDEYAGKAKAISNQAA-EEGLMILIAG 369 + + RL A IRG GL+IG LK + ++ +AA + GL+I + Sbjct: 305 QGEQLLSRLRTELAENPNVLAIRGQGLMIGIELKQ----PVRDLTLRAARDHGLLINVTR 360 Query: 370 ANVVRFAPALIISEDEV 386 +R P L I EV Sbjct: 361 GQTIRLLPPLTIDGREV 377 Lambda K H 0.321 0.137 0.412 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: 417 Number of extensions: 10 Number of successful extensions: 3 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: 391 Length adjustment: 31 Effective length of query: 375 Effective length of database: 360 Effective search space: 135000 Effective search space used: 135000 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