Align Gamma-aminobutyrate:alpha-ketoglutarate aminotransferase (EC 2.6.1.19) (characterized)
to candidate 202600 SO3497 aminotransferase, class III (NCBI ptt file)
Query= reanno::pseudo3_N2E3:AO353_08585 (454 letters) >FitnessBrowser__MR1:202600 Length = 446 Score = 292 bits (748), Expect = 1e-83 Identities = 169/435 (38%), Positives = 249/435 (57%), Gaps = 24/435 (5%) Query: 15 SSEHHLAPFSDFKQLKEKGPRIITNAKGVYLWDSEGNKILDGMAGLWCVAIGYGRDELAD 74 S EH+ PF+ +Q K PR++ A+G+Y D GNK+LD AGLWC G+GR E+++ Sbjct: 14 SLEHYWMPFTANRQFKAS-PRLLAQAEGMYYTDINGNKVLDSTAGLWCCNAGHGRREISE 72 Query: 75 AASKQMRELPYYNLFFQTAHPPVLELAKAISDIAPEGMNHVFFTGSGSEGNDTMLRMVRH 134 A SKQ+R++ Y F Q HP ELA+ +++++PEG+N VFFT SGSE DT L+M Sbjct: 73 AVSKQIRQMDYAPSF-QMGHPIAFELAERLTELSPEGLNKVFFTNSGSESVDTALKMALC 131 Query: 135 YWAIKGQPNKKVIISRINGYHGSTVAGASLGGMTYMHE--QGDLPIPGIVHIP-----QP 187 Y GQ ++ I R GYHG G S+GG++ + G L + G+ H+P Q Sbjct: 132 YHRANGQASRTRFIGREMGYHGVGFGGISVGGLSNNRKAFSGQL-LQGVDHLPHTLDIQH 190 Query: 188 YWFGEGGDMTPEEFGIWAANQLEEKILELGVDTVGAFIAEPIQGAGGVIIPPDSYWPRIK 247 F G G A LE+ + G + + A I EP+ G+ GVI+PP Y R++ Sbjct: 191 AAFSRG----LPSLGAEKAEVLEQLVTLHGAENIAAVIVEPMSGSAGVILPPQGYLKRLR 246 Query: 248 EILAKYDILFVADEVICGFGRTGEWFGSDFYGLKPDMMTIAKGLTSGYIPMGGLIVRDEV 307 EI K+ IL + DEVI FGR G F S +G+ PD++T AK + +G IPMG + V+D + Sbjct: 247 EITKKHGILLIFDEVITAFGRVGAAFASQRWGVIPDIITTAKAINNGAIPMGAVFVQDYI 306 Query: 308 VEVLNEGG----DFNHGFTYSGHPVAAAVALENIRILREEKIIEHVRAETAPYLQKRLRE 363 + +G +F HG+TYSGHPVAAA AL + I + E++ E E Y ++ + Sbjct: 307 HDTCMQGPTELIEFFHGYTYSGHPVAAAAALATLSIYQNEQLFER-SFELERYFEEAVHS 365 Query: 364 LNDHPLVGEVRGVGLLGAIELVQDKATRARYVGKGVGMICRQFCFDNGLIMRAVGDTMII 423 L P V ++R GL+ +L A ++ VGK G + CF G ++RA GD + + Sbjct: 366 LKGLPNVIDIRNTGLVAGFQL----APNSQGVGKR-GYSVFEHCFHQGTLVRATGDIIAM 420 Query: 424 APPLVITKAEIDELV 438 +PPL++ K +ID++V Sbjct: 421 SPPLIVEKHQIDQMV 435 Lambda K H 0.320 0.140 0.428 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: 505 Number of extensions: 27 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: 454 Length of database: 446 Length adjustment: 33 Effective length of query: 421 Effective length of database: 413 Effective search space: 173873 Effective search space used: 173873 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 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