Align Putative [LysW]-aminoadipate semialdehyde/glutamate semialdehyde transaminase; EC 2.6.1.- (uncharacterized)
to candidate GFF4018 Psest_4091 diaminobutyrate--2-oxoglutarate aminotransferase
Query= curated2:Q8ZV07 (383 letters) >lcl|FitnessBrowser__psRCH2:GFF4018 Psest_4091 diaminobutyrate--2-oxoglutarate aminotransferase Length = 425 Score = 176 bits (446), Expect = 1e-48 Identities = 119/370 (32%), Positives = 203/370 (54%), Gaps = 32/370 (8%) Query: 28 GQRYIDCNTNHGVVFLGHANPKIVEAVKKQVEEIWAVP-LNFATPARERFIEEFSKL-LP 85 G+RYID G + GH +P + +A+ + +E L+ T A+ERF+E F++L L Sbjct: 35 GKRYIDFLAGAGTLNYGHNHPVLKQALLEYIENDGITHGLDMYTAAKERFLETFNRLILE 94 Query: 86 PK----FGVVFLQNTGTEAVEVAIKIAKKVTRKPTIVAFTNSFHGRTMGSLSITWNEKYK 141 P+ + + F TGT AVE A+K+A+KVT + I++FTN FHG ++G+L+ T N+ ++ Sbjct: 95 PRGMGDYRMQFTGPTGTNAVEAAMKLARKVTGRNNIISFTNGFHGCSIGALAATGNQHHR 154 Query: 142 --------KAFEPLYPHVRFGKFNVPHEVDKLIGEDT------CCVVVEPIQGEGGVNPA 187 Y + K N +DKL+ + + V+VE +QGEGG+N A Sbjct: 155 GGSGISLTDVSRMPYANYFGDKTNTIGMMDKLLSDPSSGIDKPAAVIVEVVQGEGGLNTA 214 Query: 188 TPEFLKALREEAQRKGALLIFDEVQTGFGRTGAVWAFQKYGVEPDIFTAGKPVAG-GLPI 246 + E+++ L + ++ LLI D++Q G GRTG ++F++ G++PDI T K ++G GLP Sbjct: 215 STEWMRKLEKLCRKHEMLLIVDDIQAGCGRTGTFFSFEEMGIQPDIVTLSKSLSGYGLPF 274 Query: 247 GLAVAREDFGDVFEPGEHGSTFAGNAVVMAAAAAASRLLREED-----VPGRAERIGAEL 301 + + R++ D ++PGEH TF GN AAAA + D V + +RI + Sbjct: 275 AMVLLRQEL-DQWKPGEHNGTFRGNNHAFVTAAAAVEHFWQNDAFANSVKAKGKRIADGM 333 Query: 302 AKALGDTGSRLAVRVKGMGLMLGLEL--RVKADQFIQPLLERGVMALTAGVNT--LRFLP 357 + + G ++ +KG G+M+G+ A + E G++ T+G ++ ++ L Sbjct: 334 QRIIRRHGPD-SLYLKGRGMMIGISCPDGEIAAAVCRHAFENGLVIETSGAHSEVVKCLC 392 Query: 358 PYMISKEDVE 367 P +IS+E ++ Sbjct: 393 PLIISEEQID 402 Lambda K H 0.320 0.138 0.408 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: 351 Number of extensions: 23 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: 383 Length of database: 425 Length adjustment: 31 Effective length of query: 352 Effective length of database: 394 Effective search space: 138688 Effective search space used: 138688 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