Align 4-aminobutyrate aminotransferase PuuE; GABA aminotransferase; GABA-AT; Gamma-amino-N-butyrate transaminase; GABA transaminase; Glutamate:succinic semialdehyde transaminase; EC 2.6.1.19 (characterized)
to candidate GFF3422 PGA1_c34750 putative aminotransferase class 3
Query= SwissProt::P50457 (421 letters) >lcl|FitnessBrowser__Phaeo:GFF3422 PGA1_c34750 putative aminotransferase class 3 Length = 1009 Score = 144 bits (364), Expect = 9e-39 Identities = 121/399 (30%), Positives = 179/399 (44%), Gaps = 19/399 (4%) Query: 34 LKDVEGNEYIDFAAGIAVLNTGHRHPDLVAAVEQQLQQFTHTAYQIVPYESYVTLAEKIN 93 L D G Y+D A V + GH HP + A QL++ + P ++ AEKI Sbjct: 615 LFDEWGRPYLD--AYNNVPHVGHAHPRIQAIAADQLKRMNSNTRYLHPAQN--AFAEKI- 669 Query: 94 ALAPVSGQAKTAFFT-TGAEAVENAVKIARAHTGRPGVIAFSGGFHGRTYMTMALTGKVA 152 L+ + + FF +G EA E A+++ARAHTG G++ G+HG T + ++ Sbjct: 670 -LSKMPDHLEVCFFVNSGTEANELALRLARAHTGAKGMVTPDHGYHGNTTGAIDISAYKF 728 Query: 153 PYKIGFGPFPGSVYHVPYPSDLHGISTQDSLDAIER--------LFKSDIEAKQVAAIIF 204 K G GP V V D G +D ++ + K VA I Sbjct: 729 NAKGGVGPSDW-VELVEVADDYRGTYGRDDPQRAQKYADLVDPAIAKLQASGHGVAGFIA 787 Query: 205 EPVQGEGGFNVAPKELVAAIRRLCDEHGIVMIADEVQSGFARTGKL-FAMDHYADKPDLM 263 E GG + PK + A+ G + IADEVQ+G R G+ F +H PD++ Sbjct: 788 ETFPSVGGQIIPPKGYLPAVYEKIRAAGGICIADEVQTGLGRLGEYYFGFEHQGASPDIV 847 Query: 264 TMAKSLAGGMPLSGVVGNANIMDAPAPGG-LGGTYAGNPLAVAAAHAVLNIIDKESLCER 322 + K + G PL +V I D+ A G T+ G+ L+ VLNI+D+E L E Sbjct: 848 VLGKPIGNGHPLGVLVTTRAIADSFAQGPEFFSTFGGSTLSCRIGTEVLNIVDEEGLQEN 907 Query: 323 ANQLGQRLKNTLIDAKESVPAIAAVRGLGSMIAVEFNDPQTGEPSAAIAQKIQQRALAQG 382 A Q G L N L D + AI VRG+G I VE G ++ I ++ R Sbjct: 908 ARQRGADLLNGLRDLQSRHQAIGDVRGMGLFIGVELIRTD-GSEASEICAYVKNRMRDHR 966 Query: 383 LLLLTCGAYGNVIRFLYPLTIPDAQFDAAMKILQDALSD 421 +L+ + G N+++ PLTI + +K L LS+ Sbjct: 967 ILIGSEGPKDNILKIRPPLTIDAEGIEMILKTLDSILSE 1005 Lambda K H 0.319 0.134 0.388 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: 991 Number of extensions: 49 Number of successful extensions: 6 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: 421 Length of database: 1009 Length adjustment: 38 Effective length of query: 383 Effective length of database: 971 Effective search space: 371893 Effective search space used: 371893 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