Align Aspartate aminotransferase; AAT; AspAT; Putative 2-aminoadipate transaminase; Transaminase A; EC 2.6.1.1; EC 2.6.1.39 (characterized)
to candidate PfGW456L13_3206 Aspartate aminotransferase (EC 2.6.1.1)
Query= SwissProt::P58350 (410 letters) >lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3206 Aspartate aminotransferase (EC 2.6.1.1) Length = 396 Score = 213 bits (541), Expect = 1e-59 Identities = 126/380 (33%), Positives = 204/380 (53%), Gaps = 15/380 (3%) Query: 32 RAAAMKREGKPVIILGAGEPDFDTPEHVKQAASDAIHRGETKYTALDGTPELKKAIREKF 91 RA A++ +G+ +++L G+PDFDTP+ + Q A D++ G T Y + G L++AI + Sbjct: 23 RALALREQGEDILLLSVGDPDFDTPQPIVQGAIDSLLNGNTHYAEVRGKRALREAIARRH 82 Query: 92 QRENGLAYELDEITVATGAKQILFNAMMASLDPGDEVIIPTPYWTSYSDIVHICEGKPVL 151 Q+ +G + D++TV GA+ LF+ L+PGDEVI+ P + +Y + C V Sbjct: 83 QQRSGQSVSADQVTVLAGAQCALFSVAQCVLNPGDEVIVAEPMYVTYEAVFGACGAVVVP 142 Query: 152 IACDASSGFRLTAEKLEAAITPRTRWVLLNSPSNPSGAAYSAADYRPLLEVLLRHPHVWL 211 + + +GFR+ E + A ITPRTR + LNSP NPSGA+ + + L E+ + H +WL Sbjct: 143 VPVRSENGFRVLPEDVAARITPRTRALALNSPHNPSGASLPRSTWAALAELCIAH-DLWL 201 Query: 212 LVDDMYEHIVYDGFRFVTPAQLEPGLKNRTLTVNGVSKAYAMTGWRIGYAGGPRELIKAM 271 + D++Y ++++G V+PA L PG+ RT T+N +SK++AMTGWR+G+ P L + Sbjct: 202 ISDEVYSELLFEG-EHVSPASL-PGMAERTATLNSLSKSHAMTGWRVGWVVAPPSLAAHL 259 Query: 272 AVVQSQATSCPSSISQAASVAALNGPQDFLKERTESFQRRRDLVVNGLNAIDGLDCRVPE 331 + Q A+V AL L+ E++++RRDLV + L G+ P+ Sbjct: 260 ENLALCMLYGSPDFIQDAAVVALESNLPELEAMREAYRQRRDLVCDSLADCPGVRALKPD 319 Query: 332 GAFYTFSGCAGVLGKVTPSGKRIKTDTDFCAYLLEDAHVAVVPGSAFGLSP--FFRISYA 389 G + V+ + +G + F LL+ V+V+ G AFG S R+ Sbjct: 320 GGMF-------VMLDIRQTGLSAQA---FADRLLDRHGVSVLAGEAFGPSAAGHIRLGLV 369 Query: 390 TSEAELKEALERIAAACDRL 409 L++A +RIA L Sbjct: 370 VGAEPLRDACQRIARCAQEL 389 Lambda K H 0.318 0.134 0.393 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: 420 Number of extensions: 24 Number of successful extensions: 4 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: 410 Length of database: 396 Length adjustment: 31 Effective length of query: 379 Effective length of database: 365 Effective search space: 138335 Effective search space used: 138335 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 Sep 17 2021. The underlying query database was built on Sep 17 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.
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