Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate Pf1N1B4_1733 5-aminovalerate aminotransferase (EC 2.6.1.48) / Gamma-aminobutyrate:alpha-ketoglutarate aminotransferase (EC 2.6.1.19)
Query= reanno::Koxy:BWI76_RS11670 (406 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1733 Length = 425 Score = 212 bits (539), Expect = 2e-59 Identities = 137/405 (33%), Positives = 212/405 (52%), Gaps = 44/405 (10%) Query: 16 PVYAPAAFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPRLVKALTEQAGKFWHTG 75 P++A +A + + + D +G+E+IDFAGGIAV GH HP+++ A+TEQ K HT Sbjct: 25 PIFAESA------KNATVTDVEGREFIDFAGGIAVLNTGHVHPKIIAAVTEQLNKLTHTC 78 Query: 76 -NGYTNEPVLRLAKQL---IDATFADRVFFCNSGAEANEAALKLARKYAHDRFGSEKSGI 131 EP + + +++ + FA + +G+EA E ++K+AR + ++G+ Sbjct: 79 FQVLAYEPYVEVCEKINAKVPGDFAKKTLLVTTGSEAVENSIKIARA------ATGRAGV 132 Query: 132 VAFKNAFHGRTLFTVSAGGQPA-YSQDFAPLPPQIQHAIY-NDLDSAKALIDDNTC---- 185 +AF A+HGRT+ T+ G+ YS +P I A+Y N+L IDD+ Sbjct: 133 IAFTGAYHGRTMMTLGLTGKVVPYSAGMGLMPGGIFRALYPNELHGVS--IDDSIASIER 190 Query: 186 ------------AVIVEPMQGEGGVVPADADFLRGLRELCDAHNALLIFDEVQTGVGRTG 233 A+I+EP+QGEGG A +F++ LR LCD H LLI DEVQTG GRTG Sbjct: 191 IFKNDAEPRDIAAIIIEPVQGEGGFYVAPKEFMKRLRALCDQHGILLIADEVQTGAGRTG 250 Query: 234 ELYAYMHYGVTPDLLSTAKALGGGFPIGALLASERCASVMTVGTHGTTYGGNPLACAVAG 293 +A GV DL + AK++ GGFP+ + + G G TY G+P+ACA A Sbjct: 251 TFFAMEQMGVAADLTTFAKSIAGGFPLAGVCGKAEYMDAIAPGGLGGTYAGSPIACAAAL 310 Query: 294 EVFATINTREVLNGVKQRHQWFCERLNAINARYGLFKEIRGLGLLIGCVL---KDEYAGK 350 V +L+ K + L AI A+Y + E+R LG +I L D + Sbjct: 311 AVMEVFEEEHLLDRCKAVGERLVTGLKAIQAKYPVIGEVRALGAMIAVELFVDGDSHKPN 370 Query: 351 AKAISN---QAAEEGLMILIAG--ANVVRFAPALIISEDEVNSGL 390 A A+++ +A ++GL++L G NV+R L +++++ GL Sbjct: 371 AAAVASVVAKARDKGLILLSCGTYGNVLRVLVPLTSPDEQLDKGL 415 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: 445 Number of extensions: 23 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: 406 Length of database: 425 Length adjustment: 31 Effective length of query: 375 Effective length of database: 394 Effective search space: 147750 Effective search space used: 147750 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