Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate PfGW456L13_4982 Gamma-aminobutyrate:alpha-ketoglutarate aminotransferase (EC 2.6.1.19)
Query= reanno::pseudo6_N2E2:Pf6N2E2_4013 (425 letters) >lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4982 Gamma-aminobutyrate:alpha-ketoglutarate aminotransferase (EC 2.6.1.19) Length = 416 Score = 350 bits (899), Expect = e-101 Identities = 180/417 (43%), Positives = 259/417 (62%), Gaps = 6/417 (1%) Query: 12 RTAAVPRGVGQIHPIFAESAKNATVTDVEGREFIDFAGGIAVLNTGHVHPKIIAAVTEQL 71 R+ + + + +HP+ KNA V D +G+ +IDF GGI VLN GH HP+I+ A+ EQ Sbjct: 2 RSETISQSINIVHPVTLSHGKNAEVWDTDGKRYIDFVGGIGVLNLGHCHPRIVEAIREQA 61 Query: 72 NKLTHTCFQVLAYEPYVELCEKINAKVPGDFAKKTLLVTTGSEAVENAVKIARAATGRAG 131 +LTH F +EPY+EL + ++A +P + +L +G+EA ENA+KI R ATGR+ Sbjct: 62 TRLTHYAFNAAPHEPYLELMDCLSAFMPVGYPVSGMLTNSGAEAAENALKIVRGATGRSA 121 Query: 132 VIAFTGAYHGRTMMTLGLTGKVVPYSAGMGLMPGGIFRALYPNELHGVSIDDSIASIERI 191 VIAF GA+HGRT+ TL L GKV PY +G++PG +F +P+ +GV+ +++ ++ER+ Sbjct: 122 VIAFDGAFHGRTLATLNLNGKVAPYKQKVGVLPGPVFHLPFPSRDNGVTCAEALKAMERL 181 Query: 192 FKNDAEPRDIAAIIIEPVQGEGGFYVAPKEFMKRLRALCDQHGILLIADEVQTGAGRTGT 251 F + + D+A I+EPVQGE GF EF + LR CD GI+LIADE+Q+G GRTG Sbjct: 182 FSVEIDVEDVACFIVEPVQGEAGFLAMDIEFAQALRKFCDDKGIVLIADEIQSGFGRTGE 241 Query: 252 FFAMEQMGVAADLTTFAKSIAGGFPLAGVCGKAEYMDAIAPGGLGGTYAGSPIACAAALA 311 FA ++G+ DL KSIAGG PL V G+ +D + GGLGGTY+G+PIACAAALA Sbjct: 242 RFAFSRLGIEPDLILLGKSIAGGVPLGAVVGRKSLLDNLPKGGLGGTYSGNPIACAAALA 301 Query: 312 VMEVFEEEHLLDRCKAVGERLVAGLKAIQKK---YPVIGDVRALGAMIAVELFENGDSHK 368 ++ + + L E + G A + P +G + +GAM +EL N D Sbjct: 302 TLDEMNDAN-LHAWGTQQEEAIVGRHATWRANNLTPYLGRLTGVGAMRGIELI-NADG-S 358 Query: 369 PNAAAVAQVVAKARDKGLILLSCGTYGNVLRVLVPLTAPDEQLDKGLAILEECFSEL 425 P AA + Q++A ARD GL+L+ G +++R+L PLT L++GL ILE C +L Sbjct: 359 PAAAQLTQLLALARDAGLLLMPSGKSRHIIRLLAPLTIEAAVLEEGLDILEACLKKL 415 Lambda K H 0.320 0.137 0.395 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: 469 Number of extensions: 14 Number of successful extensions: 2 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: 425 Length of database: 416 Length adjustment: 32 Effective length of query: 393 Effective length of database: 384 Effective search space: 150912 Effective search space used: 150912 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 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