Align 2-aminoadipate transaminase (2.6.1.39) (characterized)
to candidate AO353_28215 AO353_28215 4-aminobutyrate aminotransferase
Query= reanno::Putida:PP_4108 (416 letters) >FitnessBrowser__pseudo3_N2E3:AO353_28215 Length = 430 Score = 353 bits (905), Expect = e-102 Identities = 190/416 (45%), Positives = 257/416 (61%), Gaps = 12/416 (2%) Query: 6 ISQSIAIVHPITLSHGRNAEVWDTDGKRYIDFVGGIGVLNLGHCNPAVVEAIQAQATRLT 65 + + + HP+ + + AE+WD DGKRY+DFVGGIGVLN+GH +P VV A+QAQ +++ Sbjct: 19 VPRGLVTAHPLVIDRAQGAELWDVDGKRYLDFVGGIGVLNIGHNHPKVVAAVQAQLQKVS 78 Query: 66 HYAFNAAPHGPYLALMEQLSQFVPVSYPLAGMLTNSGAEAAENALKVARGATGKRAIIAF 125 H F + PYL L ++L + + + SGAEA ENA+K+AR T + A+IAF Sbjct: 79 HACFQVVAYKPYLDLAQRLCEMIGGNEAYKAAFFTSGAEAVENAVKIARAHTNRSAVIAF 138 Query: 126 DGGFHGRTLATLNLNGKVAPYKQRVGELPGPVYHLPYPSADTGVTCEQALKAMDRLFSVE 185 GGFHGRTL L G PYKQ G V+H PYP+A GV+ E ALKA+D L + + Sbjct: 139 RGGFHGRTLLGTTLTGMSQPYKQNFGPFAPEVFHTPYPNAYRGVSSEMALKALDELLATQ 198 Query: 186 LAVEDVAAFIFEPVQGEGGFLALDPAFAQALRRFCDERGILIIIDEIQSGFGRTGQRFAF 245 +A E VAA I EPVQG+GGFL+ F QALR ++ GI++I+DEIQ+GFGRTG+ F F Sbjct: 199 VAPERVAAIIIEPVQGDGGFLSAPAEFLQALRALTEKHGIVLILDEIQTGFGRTGKWFGF 258 Query: 246 PRLGIEPDLLLLAKSIAGGMPLGAVVGRKELMAALPKGGLGGTYSGNPISCAAALASLAQ 305 GI+PDL+ +AKS+AGG+PL VVG+ +M A GGLGGTY GN +SCAAALA + Sbjct: 259 QHAGIQPDLVTVAKSLAGGLPLSGVVGKAGIMDAPLPGGLGGTYGGNALSCAAALAVIDA 318 Query: 306 MTDENLA----TWGERQEQAIVSRYERWKASGLSPYIGRLTGVGAMRGIEFANADGSPAP 361 E L GER Q ++ R + IG + G G M IE D + P Sbjct: 319 YEQEQLLARGDALGERLRQGLLRLQARHR------QIGDVRGSGFMLAIELIKDDDARTP 372 Query: 362 -AQL-AKVMEAARARGLLLMPSGKARHIIRLLAPLTIEAEVLEEGLDILEQCLAEL 415 A L ++++ ARA GLL++ G R+++R LAPL + ++E L ILE LA + Sbjct: 373 DADLNQRLIDEARAGGLLVIKCGVYRNVLRFLAPLVTTEDQIDEALQILEAALARV 428 Lambda K H 0.320 0.137 0.402 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: 535 Number of extensions: 15 Number of successful extensions: 2 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: 416 Length of database: 430 Length adjustment: 32 Effective length of query: 384 Effective length of database: 398 Effective search space: 152832 Effective search space used: 152832 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