Align L-lysine 6-transaminase (EC 2.6.1.36) (characterized)
to candidate Pf1N1B4_4553 FIG00959354: hypothetical protein
Query= BRENDA::Q5XPV2 (457 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4553 Length = 956 Score = 93.2 bits (230), Expect = 3e-23 Identities = 87/288 (30%), Positives = 128/288 (44%), Gaps = 31/288 (10%) Query: 165 LERSFHGRSGYTMSLTNTEPSKTARFPKFGWP-RISSPA----LQHPPAEHTG--ANQEA 217 L SFHG+ T+ LT + + F +FG P LQ PA HT + Sbjct: 204 LRGSFHGKLVNTVQLTYGKQYRQP-FARFGLNVEFIDPQQPHQLQELPARHTRHWLTLQW 262 Query: 218 ERRALEAAREAFAAADGMIACFIAEPIQGEGGDNHLSAEFLQAMQRLCHENDALFVLDEV 277 L R+AF+A I + EPIQGEGG +A+F A++RLC+E ++DEV Sbjct: 263 SGEQLLVGRQAFSA----ITAVLLEPIQGEGGIIEFAADFYLALRRLCNEQQCPLIVDEV 318 Query: 278 QSGCGITGTAWAYQQLGLQPDLVAFGKKTQVCGVMGGGRIDEVP--------ENVFAVSS 329 QSG G TGT A LQ D K +GGG + EN F+ Sbjct: 319 QSGFGRTGTFLASSHFNLQGDYYCLSK------ALGGGLMKIAATVIRSSHYENDFSYIH 372 Query: 330 RISSTWGGNLADMVRATRLLETI--ERTQVFDTVVQRGKYFRDGLEDLAARHPSVVTNAR 387 SST+ + A A L + + + V +G+Y + L +L A +P V+ + R Sbjct: 373 --SSTFAEDDASCHIALSALNRLFADDNAMLKDVHNKGEYLKTSLLELKAAYPDVIADVR 430 Query: 388 GRGLMCAVDLPDTRTRNEVLRLMYTEHQVIALPCGGRSLRFRPALTIA 435 GRGL+ +L D + +++ + + G L+F AL +A Sbjct: 431 GRGLLLGFELHDQSGNSSLVQASAQYNDALGYLIAGYLLQFE-ALRVA 477 Lambda K H 0.320 0.135 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: 815 Number of extensions: 39 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: 457 Length of database: 956 Length adjustment: 38 Effective length of query: 419 Effective length of database: 918 Effective search space: 384642 Effective search space used: 384642 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: 54 (25.4 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