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_015887459.1 NGR_RS06525 4-aminobutyrate--2-oxoglutarate transaminase
Query= SwissProt::P50457 (421 letters) >NCBI__GCF_000018545.1:WP_015887459.1 Length = 422 Score = 523 bits (1347), Expect = e-153 Identities = 257/411 (62%), Positives = 315/411 (76%) Query: 9 RRLSATPRGVGVMCNFFAQSAENATLKDVEGNEYIDFAAGIAVLNTGHRHPDLVAAVEQQ 68 R+ +A RGVG+ +A AENA + D E N YIDFAAGIAV+NTGHRHP ++AAV+ Q Sbjct: 7 RKNAAISRGVGMTTQIYADRAENAEIWDKESNRYIDFAAGIAVVNTGHRHPKVIAAVKAQ 66 Query: 69 LQQFTHTAYQIVPYESYVTLAEKINALAPVSGQAKTAFFTTGAEAVENAVKIARAHTGRP 128 L +FTHT +Q+VPYE+YV LAE++NALAP KT F TTGAEAVENAVKIARA TGR Sbjct: 67 LDRFTHTCHQVVPYENYVHLAERLNALAPGKFAKKTIFVTTGAEAVENAVKIARAATGRQ 126 Query: 129 GVIAFSGGFHGRTYMTMALTGKVAPYKIGFGPFPGSVYHVPYPSDLHGISTQDSLDAIER 188 VIAF GGFHGRT+M MALTGKV PYK+GFG P V+H P+P +LHG+S + SL A+++ Sbjct: 127 AVIAFGGGFHGRTFMGMALTGKVVPYKVGFGAMPADVFHAPFPIELHGVSVEQSLAALKK 186 Query: 189 LFKSDIEAKQVAAIIFEPVQGEGGFNVAPKELVAAIRRLCDEHGIVMIADEVQSGFARTG 248 LF +D++ +VAAII EPVQGEGGF AP + A+R +CD+HGI++IADEVQ+GFARTG Sbjct: 187 LFAADVDPGRVAAIILEPVQGEGGFYPAPTAFMKALREICDQHGILLIADEVQTGFARTG 246 Query: 249 KLFAMDHYADKPDLMTMAKSLAGGMPLSGVVGNANIMDAPAPGGLGGTYAGNPLAVAAAH 308 KLFAM+H+ PDLMTMAKSLAGG PL+ V G A IMDAP PGGLGGTY GNP+ +AAAH Sbjct: 247 KLFAMEHHDVAPDLMTMAKSLAGGFPLAAVTGRAEIMDAPGPGGLGGTYGGNPIGIAAAH 306 Query: 309 AVLNIIDKESLCERANQLGQRLKNTLIDAKESVPAIAAVRGLGSMIAVEFNDPQTGEPSA 368 AVL++I++E LCERANQLG RLK L +E P I +RG G M AVEFND +T PSA Sbjct: 307 AVLDVIEEEQLCERANQLGNRLKQRLAQIREKAPEIVDIRGPGFMNAVEFNDVKTKLPSA 366 Query: 369 AIAQKIQQRALAQGLLLLTCGAYGNVIRFLYPLTIPDAQFDAAMKILQDAL 419 A K++ AL +GL+LLTCG +GNVIRFL P+TI D F A+ IL+ ++ Sbjct: 367 EFANKVRLIALEKGLILLTCGVHGNVIRFLAPITIQDEVFAEALDILEASI 417 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: 606 Number of extensions: 22 Number of successful extensions: 1 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: 422 Length adjustment: 32 Effective length of query: 389 Effective length of database: 390 Effective search space: 151710 Effective search space used: 151710 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: 50 (23.9 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