Align Gamma aminobutyrate transaminase 1, mitochondrial; Gamma-aminobutyrate transaminase isozyme 1; LeGABA-TP1; SlGABA-T1; EC 2.6.1.96 (characterized)
to candidate WP_015931963.1 MNOD_RS26085 aminotransferase
Query= SwissProt::Q84P54 (515 letters) >NCBI__GCF_000022085.1:WP_015931963.1 Length = 460 Score = 429 bits (1103), Expect = e-124 Identities = 219/437 (50%), Positives = 291/437 (66%), Gaps = 2/437 (0%) Query: 69 MLAPFTAGWQSTDVDPLIIEKSEGSHVYDMQGRKYIDTLAGLWCTALGGNEPRLVDAATK 128 ++ P+T Q + PL++E+ G VYD GR YI+ +AGLWCTALG + LV+AA + Sbjct: 13 LIHPYTNLAQFRESGPLVLERGHGVWVYDTDGRPYIEGMAGLWCTALGYSNEELVEAARE 72 Query: 129 QLNTLPFYHSFWNRTTKPSLDLAKELLDMFTAKKMAKAFFTNSGSEANDTQVKLVWYYNN 188 Q+ LPF H F R+ P+++L ELL ++K FFT+SGSEANDTQVKL WY NN Sbjct: 73 QMARLPFSHLFSGRSHDPAIELG-ELLKELAPIPVSKVFFTSSGSEANDTQVKLTWYLNN 131 Query: 189 ALGRPNKKKFIARAKAYHGSTLISASLTGLPALHQNFDLPAPFVLHTDCPHYWRYHLPGE 248 ALGRP KKK I+ K YHG T+ SASLTGL A H ++DLP P LH CPH++R PGE Sbjct: 132 ALGRPRKKKIISHTKGYHGVTVASASLTGLTANHADWDLPLPGFLHATCPHHYRNAQPGE 191 Query: 249 TEEEFSTRLAKNLEDLILKEGPETIAAFIAEPVMGAGGVIPPPATYFDKIQAVVKKYDIL 308 +EE FS RLA L+ LI +E P+T+AAFIAEPVMGAGG I PP YF I+ V+ YDI Sbjct: 192 SEEAFSARLAAELDALIQREDPDTVAAFIAEPVMGAGGAIVPPKGYFAAIEPVLAAYDIR 251 Query: 309 FIADEVICAFGRLGTMFGSDMYNIKPDLVTLAKALSSAYMPIGAVLVSPEVSDVIHSQSN 368 FIADEVIC FGRLGT FG++ ++P ++ AKA++SAYMP+G + V + + +S Sbjct: 252 FIADEVICGFGRLGTWFGAETMAMRPQSLSFAKAVTSAYMPLGGLTVEEPLYQAMLEESR 311 Query: 369 KLGSFSHGFTYSGHPVACAVALEAIKIYKERNMVERVNRISPKFQEGLKAFSDSPIIGEI 428 K+GSF HG TYSGHPVACAVA++ ++IY+ +VE +P FQ L+A ++ P++GE Sbjct: 312 KIGSFGHGTTYSGHPVACAVAIKTLEIYRRDRLVEAAAEKAPHFQRRLEALAEHPLVGEA 371 Query: 429 RGLGLILATEFANNKSPNDHFPPEWGVGAYFGAQCQKNGMLVR-VAGDTIMMSPPFVVTP 487 RG+GLI E +K+ + P+ GV A A Q G++VR +AGD I + PP V+ P Sbjct: 372 RGVGLIGGLEIVADKATKRQYDPKAGVAARCVAFAQGEGLIVRFLAGDRIAVCPPLVIVP 431 Query: 488 EELDELIRIYGKALRET 504 +E+D L +AL T Sbjct: 432 DEIDALFDRLTRALDRT 448 Lambda K H 0.318 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: 570 Number of extensions: 16 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: 515 Length of database: 460 Length adjustment: 34 Effective length of query: 481 Effective length of database: 426 Effective search space: 204906 Effective search space used: 204906 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 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