Align Putative [LysW]-aminoadipate semialdehyde/glutamate semialdehyde transaminase; EC 2.6.1.- (uncharacterized)
to candidate 208056 DVU2559 adenosylmethionine--8-amino-7-oxononanoate aminotransferase
Query= curated2:Q9YBY6 (388 letters) >lcl|MicrobesOnline__882:208056 DVU2559 adenosylmethionine--8-amino-7-oxononanoate aminotransferase Length = 542 Score = 123 bits (309), Expect = 1e-32 Identities = 124/408 (30%), Positives = 187/408 (45%), Gaps = 57/408 (13%) Query: 28 DDSGRKYLDCHAGHGAAFLGHSNPAIVEAVVRQARELVAASSSFS---TPSLEEALTEFS 84 D G +YLD + GH +P I EA+ RQ + VA S+ TPS+E A + Sbjct: 97 DTDGNRYLDGVSSLWTNVHGHRHPHIDEAIRRQL-DRVAHSTLLGLGGTPSIELA-ARLT 154 Query: 85 RIAPPWAEEIVFLNTGTEAVEAALKAAWLA--------TGKRGIVALKNSFHGRTLASLS 136 IAP + + ++G+ AVEAALK A+ + ++A N++HG T+ S+S Sbjct: 155 AIAPAGLTRVFYSDSGSTAVEAALKIAFQYHRQAPEGDARRTRVMAFSNAYHGDTIGSVS 214 Query: 137 VTWNPRYRRGV--PVLDTRFLSPSTDP-----------------GEVEKLVPE---DTAA 174 + + G+ P+L +P+ GEVE+L+ + A Sbjct: 215 LGGMSLFH-GIYGPLLFDPVRAPAPHCYRCPADLRPETCGMACLGEVERLMRHHGHELCA 273 Query: 175 IIVEP-IQGEGGLTKIYAELAKALREAADRVGALLIFDEIQTGFGRTGRVWAHESLGVEP 233 ++VEP +QG G+ + LR+ DR G ++ DE+ GFG+TG ++A E GV P Sbjct: 274 VVVEPLVQGAAGMLVQPRGWLRGLRDLCDRHGVFMVADEVAVGFGKTGTMFACEQEGVVP 333 Query: 234 DIMTAGKSIAGG-LPASAVLSRE----GVLATLASGR---HGSTHAANPLSMAAVAAASR 285 D++ K I GG LP +A L E G L A R HG T+ N L+ AA A+ Sbjct: 334 DMLCLAKGITGGYLPLAATLVTEHIHDGFLGGYADFRTFFHGHTYTGNALACAAALASLD 393 Query: 286 FLREEGVPDKARAAGALLEGLLRDRIEGLRLVRGVRGEGLMLGVEL------RLDPGPVL 339 EE + R L LL + L V +R G+M G+EL R P Sbjct: 394 VFEEERTLETLRPRIERLATLLAP-LNDLPHVGDIRRVGVMTGIELVADRETRTPYRPEE 452 Query: 340 R-----CLQESERVLALRSGATVVRLLPPYSISREDAEMVVYGLERCI 382 R L+ R + +R V+ L+PP SI+ + E +V+ + I Sbjct: 453 RIGHRVTLEARRRGVIVRPLGDVMVLMPPLSITETELETLVHTVRGAI 500 Lambda K H 0.319 0.136 0.398 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: 479 Number of extensions: 29 Number of successful extensions: 1 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: 388 Length of database: 542 Length adjustment: 33 Effective length of query: 355 Effective length of database: 509 Effective search space: 180695 Effective search space used: 180695 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: 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