Align Gamma aminobutyrate transaminase 3, chloroplastic; Gamma-aminobutyrate transaminase isozyme 3; LeGABA-TP3; SlGABA-T3; EC 2.6.1.96 (characterized)
to candidate SM_b20423 SM_b20423 hypothetical protein
Query= SwissProt::Q84P52 (520 letters) >FitnessBrowser__Smeli:SM_b20423 Length = 458 Score = 364 bits (934), Expect = e-105 Identities = 183/433 (42%), Positives = 271/433 (62%), Gaps = 9/433 (2%) Query: 76 GWHSTDLEPL-VIQKSEGSYVYDVNGKKYLDALAGLWCTSLGGNEPRLVAAATKQLNELA 134 G H+ P VI EG Y+ D++GK+ LDA AGL+C ++G ++ A +Q LA Sbjct: 24 GMHARGETPTRVIGGGEGVYITDISGKRSLDAFAGLYCVNVGYGRQKIADAIAEQAKNLA 83 Query: 135 FYHSFWNRSTKPSLDLAKELLDLFTANKMAKAFFTNSGSEANDTQVKLVWYYNNALGRPD 194 +YH++ T+ S+ L+K ++D M++ +F SGS+AN+T +KL+WYYNN LGRP+ Sbjct: 84 YYHAYVGHGTEASIRLSKMIIDR-APEGMSRVYFGLSGSDANETNIKLIWYYNNILGRPE 142 Query: 195 KKKFIARTKSYHGSTLISASLSGLPALHQQFDLPAPFVLHTDCPHFWRFHQPGETEEEFS 254 KKK I+R + YHGS +++ SL+GL H FDLP +LHT+ P+++R +EE+FS Sbjct: 143 KKKIISRWRGYHGSGVMTGSLTGLHLFHNAFDLPRAPILHTEAPYYFRRPDRSMSEEQFS 202 Query: 255 TRLANNLENLILKEGPETIAAFIAEPVMGAGGVIPPPATYFEKVQAILKKYDILFIADEV 314 A+ LE +IL EGP+T+AAFI EP++G GG++PPP Y+EK+QA+L+KYDIL +ADEV Sbjct: 203 QYCADKLEEMILAEGPDTVAAFIGEPILGTGGIVPPPKGYWEKIQAVLQKYDILLVADEV 262 Query: 315 ICGFGRLGTMFGCEKYNIKPDLVSVAKALSSGYMPIGAVLVSPEVSDVIYSQSNKLGTFS 374 + GFGRLGTMFG + Y IKPDL+++AK L+S Y P+ +VS ++ V+ S++LG Sbjct: 263 VTGFGRLGTMFGSDHYGIKPDLITIAKGLTSAYAPLSGTIVSDKLWQVLVKGSDELGAIG 322 Query: 375 HGFTYSGHPVSCAVALETLKIYKERNIIEQVNRISPKFQEGL-KAFSDSPIIGEIRGTGL 433 HG+TYS HP+ A + L++ E I+E F+ L KA D +GE+RG GL Sbjct: 323 HGWTYSAHPICAAAGIANLELIDELGIVENAGSTGAYFRAELQKAVGDHRHVGEVRGDGL 382 Query: 434 LHGTEFTDNKSPNDPFPPEWGIGAYFGARCEKHGVLVRV--AGDNIMMSPPYILSLEEID 491 + EF +++ F P +G A + GV+ R GD + +PP L+ +E D Sbjct: 383 MAAIEFVEDRDDRAFFDPGRKVGPQVAAALLERGVIGRAMPQGDILGFAPPLCLTRDEAD 442 Query: 492 ELIIKYGKALKDT 504 ++ KA DT Sbjct: 443 IVV----KAAADT 451 Lambda K H 0.317 0.135 0.401 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: 628 Number of extensions: 21 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: 520 Length of database: 458 Length adjustment: 34 Effective length of query: 486 Effective length of database: 424 Effective search space: 206064 Effective search space used: 206064 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 (21.6 bits) S2: 52 (24.6 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