Align glutamate N-acetyltransferase/amino-acid acetyltransferase; EC 2.3.1.35 2.3.1.1 (characterized)
to candidate HSERO_RS01730 HSERO_RS01730 N-acetylglutamate synthase
Query= CharProtDB::CH_000559 (406 letters) >FitnessBrowser__HerbieS:HSERO_RS01730 Length = 411 Score = 421 bits (1082), Expect = e-122 Identities = 229/413 (55%), Positives = 287/413 (69%), Gaps = 9/413 (2%) Query: 1 MAVNLTEKTAEQLPDIDGIALYTAQAGVKKPGHTDLTLIAVAAGSTVGAVFTTNRFCAAP 60 MAVN L + GI L A+AGV+K D+ ++ +A +TV VFT NRFCAAP Sbjct: 1 MAVNSPIPVPSDLKAVAGIELGHAEAGVRKANRKDVLVMKLAETATVAGVFTKNRFCAAP 60 Query: 61 VHIAKSHLFDEDG---VRALVINTGNANAGTGAQGRIDALAVCAAAARQIGCKPNQVMPF 117 V I +++L +RALVINTGNANAGTG +G A +VCAA A+Q+G + Q++PF Sbjct: 61 VQICQANLAQLSAGKPIRALVINTGNANAGTGEEGLQRAKSVCAALAQQMGVEAQQILPF 120 Query: 118 STGVILEPLPADKIIAALPK----MQPAFWNEAARAIMTTDTVPKAASREGKVGDQHTVR 173 STGVILEPLPAD+IIA LP+ ++ W AA +IMTTDT PKAASR +G + V Sbjct: 121 STGVILEPLPADRIIAGLPQAIGNLKADNWFNAAESIMTTDTQPKAASRTLTIGGKQVVM 180 Query: 174 ATGIAKGSGMIHPNMATMLGFIATDAKVSQPVLQLMTQEIADETFNTITVDGDTSTNDSF 233 TGI+KG+GMI PNMATMLGF+A DAK+ Q +L + ++ AD +FN IT+DGDTSTNDSF Sbjct: 181 -TGISKGAGMIKPNMATMLGFLAFDAKLPQALLNQLVKDAADHSFNCITIDGDTSTNDSF 239 Query: 234 VIIATGKNSQSEIDNIADPRYAQLKELLCSLALELAQAIVRDGEGATKFITVRVENAKTC 293 +++ATG + EI + Y QL + L+ LA IVRDGEGATKFI V VE+ K+ Sbjct: 240 ILMATGAG-ELEITSADSEEYQQLAAAVTDLSQHLAHQIVRDGEGATKFIEVAVEDGKSV 298 Query: 294 DEARQAAYAAARSPLVKTAFFASDPNLGKRLAAIGYADVADLDTDLVEMYLDDILVAEHG 353 +E RQ AY+ SPLVKTAFFASDPNLG+ LAAIGYA + DLD + ++LDD+ VA+ G Sbjct: 299 EECRQIAYSIGHSPLVKTAFFASDPNLGRILAAIGYAGIDDLDVSKINLWLDDVWVAKDG 358 Query: 354 GRAASYTEAQGQAVMSKDEITVRIKLHRGQAAATVYTCDLSHGYVSINADYRS 406 GR Y E GQ VM K EI VR+KL RG A A+++TCDLSH YVSINADYRS Sbjct: 359 GRNPDYREEDGQRVMKKAEIVVRVKLARGAAKASIWTCDLSHDYVSINADYRS 411 Lambda K H 0.317 0.130 0.367 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: 381 Number of extensions: 10 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: 406 Length of database: 411 Length adjustment: 31 Effective length of query: 375 Effective length of database: 380 Effective search space: 142500 Effective search space used: 142500 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 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