Align Acetylornithine aminotransferase; ACOAT; EC 2.6.1.11 (uncharacterized)
to candidate N515DRAFT_3630 N515DRAFT_3630 4-aminobutyrate aminotransferase
Query= curated2:Q97GH9 (387 letters) >lcl|FitnessBrowser__Dyella79:N515DRAFT_3630 N515DRAFT_3630 4-aminobutyrate aminotransferase Length = 469 Score = 153 bits (386), Expect = 1e-41 Identities = 113/428 (26%), Positives = 198/428 (46%), Gaps = 68/428 (15%) Query: 17 FDKGEGTKLYDKDGNEYIDFVSGVAVNCLGHCNPSIVKAIEEQSSKLMHVSNYYWNENAM 76 F G+G+ +YD G ++D + G+ N + ++ Q L V++ Y ++ + Sbjct: 41 FRHGQGSWMYDTAGVPFLDLQMWYSAVNFGYGNKRLNDTLKAQIDTLPQVASQYLHQTRI 100 Query: 77 ELTEILCKNSEFD-----KVFMCNSGTEAIEAGLKLARKYALLHGDENKKEIIY-MDNSF 130 EL + + +++ +V G +A+E LKL R Y +N K +++ + + Sbjct: 101 ELAKTIAVDAQQKFGLKGRVHFNVGGAQAVEDSLKLVRNY------KNGKSLMFAFEGGY 154 Query: 131 HGRTMGALSVTGQPKYQESFKPL-------------------------------IGAVKS 159 HGRT+GA S+T +Y+ F + Sbjct: 155 HGRTLGASSITSSYRYRRRFGHFGERAMFIPFPYPFRRPKGMTPEEYSDACVRQFERLFE 214 Query: 160 VKFNDLDDIKQKISSKTAAVIVEPIQGEGGIIPAKKEYLKLLRDLCDENNALLIFDEVQC 219 ++N + D K ++ AA VEPIQG GG + K + K L+ + D+ L++ DE+Q Sbjct: 215 TEYNGVWDPKVN-QAEYAAFYVEPIQGTGGYVIPPKNFFKDLKKVLDKYGILMVVDEIQM 273 Query: 220 GMGRVGSLFAYQKFEVVPDIVCIAKALGGGF-PIGAMLAKESVASS--FVPGDHGNTYGG 276 G R G L++ + F V PDI+ KAL G P+ + A+E + + F PG +T+ Sbjct: 274 GFWRTGKLWSIEHFGVTPDIIVFGKALTNGLNPLSGLWAREEMINPEIFPPGSTHSTFNS 333 Query: 277 NPLACAVAIAVLKELVDKKVVEINVNEKSKYLFDKLMTLKEKYKVINDVRGMGLLIGVEV 336 NPL ++ + V+K + + E NV +K + D L L++++K I DV G+GL + E+ Sbjct: 334 NPLGTSLGLEVIK-MGYELDYETNVAKKGAHFLDALKDLQKRHKEIGDVDGLGLALRAEI 392 Query: 337 ACDVKKIINKCFESKL-----------------LLITAG---KNVVRFLPPLNVSFEEID 376 D NK ++ L++ G KNV+ F P L+++ EEID Sbjct: 393 CTDDGFTPNKALLDRMVDIGLAGDLEHNGKKIGLVLDVGGWYKNVITFAPSLDITHEEID 452 Query: 377 KALGIFEE 384 A+ + ++ Sbjct: 453 LAIALLDQ 460 Lambda K H 0.318 0.137 0.395 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: 393 Number of extensions: 20 Number of successful extensions: 7 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 387 Length of database: 469 Length adjustment: 32 Effective length of query: 355 Effective length of database: 437 Effective search space: 155135 Effective search space used: 155135 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: 51 (24.3 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