Align glutamate N-acetyltransferase/amino-acid acetyltransferase; EC 2.3.1.35 2.3.1.1 (characterized)
to candidate RR42_RS18020 RR42_RS18020 ornithine acetyltransferase
Query= CharProtDB::CH_000559 (406 letters) >FitnessBrowser__Cup4G11:RR42_RS18020 Length = 409 Score = 455 bits (1171), Expect = e-132 Identities = 243/410 (59%), Positives = 290/410 (70%), Gaps = 5/410 (1%) Query: 1 MAVNLTEKTAEQLPDIDGIALYTAQAGVKKPGHTDLTLIAVAAGSTVGAVFTTNRFCAAP 60 MAVNL AE L + G+ L A+AGV+K D+ ++ VA GSTV VFT NRFCAAP Sbjct: 1 MAVNLPLPLAENLKPVAGVELGWAEAGVRKANRKDVLVVRVAQGSTVAGVFTRNRFCAAP 60 Query: 61 VHIAKSHLFDEDGVRALVINTGNANAGTGAQGRIDALAVCAAAARQIGCKPNQVMPFSTG 120 V + + HL G+RA+V+NTGNANAGTG G +A A C A A Q+G P QV+PFSTG Sbjct: 61 VQVCREHLAAGKGIRAIVVNTGNANAGTGEPGLANARATCDALAAQLGIAPEQVLPFSTG 120 Query: 121 VILEPLPADKIIAALP----KMQPAFWNEAARAIMTTDTVPKAASREGKVGDQHTVRATG 176 VILEPLP D+I AALP +P W AA +IMTTDT PKAASR ++G + TV +G Sbjct: 121 VILEPLPVDRITAALPAAIANAKPDNWLAAAESIMTTDTQPKAASRTVQIGGK-TVTLSG 179 Query: 177 IAKGSGMIHPNMATMLGFIATDAKVSQPVLQLMTQEIADETFNTITVDGDTSTNDSFVII 236 I+KG+GMI PNMATMLGF+ATDA VSQ VLQ + AD +FN+IT+DGDTSTNDSFV+I Sbjct: 180 ISKGAGMIRPNMATMLGFVATDATVSQDVLQALVSYAADHSFNSITIDGDTSTNDSFVLI 239 Query: 237 ATGKNSQSEIDNIADPRYAQLKELLCSLALELAQAIVRDGEGATKFITVRVENAKTCDEA 296 A+GK I+ + L+ L L+ ELAQ IVRDGEGATK +T++VE K E Sbjct: 240 ASGKAGAPAIERAEGADFEALRAALTDLSQELAQMIVRDGEGATKLMTIQVEGGKDVAEC 299 Query: 297 RQAAYAAARSPLVKTAFFASDPNLGKRLAAIGYADVADLDTDLVEMYLDDILVAEHGGRA 356 R AYA A SPLVKTAF+ASDPNLG+ LAA+GYA V DLD + V ++LDD+LVA GGR Sbjct: 300 RLIAYAVAHSPLVKTAFYASDPNLGRILAAVGYAGVDDLDVERVNLWLDDVLVARDGGRN 359 Query: 357 ASYTEAQGQAVMSKDEITVRIKLHRGQAAATVYTCDLSHGYVSINADYRS 406 Y E GQ VM + EITVRI L RG AAATV+TCDLSH YVSINADYRS Sbjct: 360 PEYREEDGQRVMKQAEITVRIALGRGDAAATVWTCDLSHDYVSINADYRS 409 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: 433 Number of extensions: 8 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: 409 Length adjustment: 31 Effective length of query: 375 Effective length of database: 378 Effective search space: 141750 Effective search space used: 141750 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