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 WP_074200562.1 BUQ81_RS01125 adenosylmethionine--8-amino-7-oxononanoate transaminase
Query= SwissProt::P50457 (421 letters) >NCBI__GCF_900141795.1:WP_074200562.1 Length = 428 Score = 136 bits (343), Expect = 1e-36 Identities = 109/366 (29%), Positives = 172/366 (46%), Gaps = 23/366 (6%) Query: 38 EGNEYIDFAAGIAVLNTGHRHPDLVAAVEQQLQQFTHTAYQIVPYESYVTLAEKINALAP 97 +G +D + G+ HP+LV AV +QL+ H + + +E V LAEK+ L+P Sbjct: 39 DGRRLVDGMSSWWAAIHGYNHPELVLAVARQLKTMPHIMFGGLTHEPAVDLAEKLVTLSP 98 Query: 98 VSGQAKTAFFTTGAEAVENAVKIA------RAHTGRPGVIAFSGGFHGRTYMTMALTGKV 151 V + K F +G+ AVE A+KIA R + + G+HG T+ M++T Sbjct: 99 VPLK-KVFFADSGSVAVEVALKIALQYWMARRKPQKHIFLTVRNGYHGDTFGAMSVTDPD 157 Query: 152 APYKIGFGPFPGSVYHVPYPSDLHGISTQDSLDAIERLFKS-DIEAKQVAAIIFEP-VQG 209 F Y P P + + D I L D ++AAII EP VQG Sbjct: 158 NGMHSLFAGVLPKHYFAPAPHMGFDLKLDEPADDIAALAAFLDHHHDEIAAIILEPIVQG 217 Query: 210 EGGFNVAPKELVAAIRRLCDEHGIVMIADEVQSGFARTGKLFAMDHYADKPDLMTMAKSL 269 GG V +R + D++ +++I DE+ +GF RTGKLFA + PD+MT+ K+L Sbjct: 218 AGGMRFYRPAYVRQLRAIADDYNVLLIFDEIATGFGRTGKLFACEWAGISPDIMTVGKAL 277 Query: 270 AGG-MPLSGVVGNANIM-----DAPAPGGLGGTYAGNPLAVAAAHAVLNIIDKESLCERA 323 GG M L+ + + + P G T+ NP A AAA+A + ++ K + +R Sbjct: 278 TGGMMTLAATLTTEEVAYTLCNNPPRALMHGPTFMANPTACAAANASIELLLKSAWQDRI 337 Query: 324 NQLGQRLKNTLIDAKESVPAIAAVRGLGSMIAVEFNDPQTGEPSAAIAQKIQQRALAQGL 383 + L+ L+ + P +A VR LG++ +E +A ++Q A+ +G Sbjct: 338 QHIEAHLQEQLMPLSDH-PGVADVRVLGAIGVIELERDD-------LAPRLQDMAVREGA 389 Query: 384 LLLTCG 389 L G Sbjct: 390 WLRPFG 395 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: 449 Number of extensions: 28 Number of successful extensions: 3 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: 428 Length adjustment: 32 Effective length of query: 389 Effective length of database: 396 Effective search space: 154044 Effective search space used: 154044 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: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. 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:
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