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_033101175.1 JG50_RS0110325 aspartate aminotransferase family protein
Query= SwissProt::P50457 (421 letters) >NCBI__GCF_000763315.1:WP_033101175.1 Length = 448 Score = 209 bits (533), Expect = 1e-58 Identities = 148/442 (33%), Positives = 229/442 (51%), Gaps = 34/442 (7%) Query: 1 MSNNEFHQRRLSATPRGVGVMCNFFAQSAENATLKDVEGNEYIDFAAGIAVLNTGHRHPD 60 ++N E + + PR + + + A +KDVEG Y D +G L GH HP Sbjct: 9 LANQERRESNARSYPRRIPIAI----KEANGIFVKDVEGKVYYDCLSGAGTLALGHNHPV 64 Query: 61 LVAAVEQQLQQFT--HTAYQIVPYESYVTLAEKINALAPVS--GQAKTAFFT-TGAEAVE 115 ++ A+ Q L HT P + E++ A P S +AK F + +GA+AVE Sbjct: 65 VIEAIRQVLDSRLPLHTLDLTTPVKD--EFIEELFASLPKSFASRAKVQFCSPSGADAVE 122 Query: 116 NAVKIARAHTGRPGVIAFSGGFHGRTYMTMALTGKVAPYK--------IGFGPFPGSVYH 167 A+K+ + TGR + +F G FHG T+ ++LTG +AP + + F P+P Y Sbjct: 123 AAIKLVKTATGRRTLFSFHGAFHGMTHGALSLTGNLAPKQPIANLMPDVHFLPYP---YA 179 Query: 168 VPYPSDLHG-ISTQDSLDAIERLFKS-DIEAKQVAAIIFEPVQGEGGFNVAPKELVAAIR 225 P +L G + Q + I+R+ + A +I E VQGEGG AP V ++R Sbjct: 180 YRCPFNLGGTLGEQTGIHYIKRVLNDPESGIAPPAGMIMEIVQGEGGVIPAPDNWVQSVR 239 Query: 226 RLCDEHGIVMIADEVQSGFARTGKLFAMDHYADKPDLMTMAKSLAGGMPLSGVVGNANIM 285 + EH + +I DEVQ+GF RTGKLFA +H PD++ ++KS+ G +PL+ VV + + + Sbjct: 240 SITREHKVPLIVDEVQTGFGRTGKLFAFEHAGIIPDVLVLSKSIGGSLPLAVVVYDQS-L 298 Query: 286 DAPAPGGLGGTYAGNPLAVAAAHAVLNIIDKESLCERANQLGQRLKNTLIDAKESVPAIA 345 D +PG GT+ GN +A+AA A + I L A Q+G+RL + L + I Sbjct: 299 DQWSPGAHTGTFRGNQMAMAAGIATIRFIRDNRLEVNAAQMGERLMSRLKSIQNESTCIG 358 Query: 346 AVRGLGSMIAVEFNDPQTGEPSA--------AIAQKIQQRALAQGLLLLTCGAYGNVIRF 397 VRG G +I VE + Q EP + +A++IQ+ + +GL+L G +G+V+RF Sbjct: 359 DVRGRGLLIGVEIVNTQR-EPDSLGSYPAYPELARQIQRESFNRGLILELGGRHGSVVRF 417 Query: 398 LYPLTIPDAQFDAAMKILQDAL 419 L PL I Q + + +A+ Sbjct: 418 LPPLIITGEQVEHISAVFAEAV 439 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: 490 Number of extensions: 23 Number of successful extensions: 5 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: 448 Length adjustment: 32 Effective length of query: 389 Effective length of database: 416 Effective search space: 161824 Effective search space used: 161824 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 Sep 24 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:
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