Align L-piperidine-6-carboxylate dehydrogenase; EC 1.2.1.21 (characterized, see rationale)
to candidate Ga0059261_1495 Ga0059261_1495 succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71)
Query= uniprot:Q88CC3 (496 letters) >FitnessBrowser__Korea:Ga0059261_1495 Length = 480 Score = 175 bits (443), Expect = 4e-48 Identities = 141/467 (30%), Positives = 221/467 (47%), Gaps = 39/467 (8%) Query: 19 GDYPVHTPIDGSQIASVKLLGKA--------ETIARIDQAQSAFEAWRSVPAPRRGELVR 70 G P + GS+I S + A + A + A++++ W + P R E +R Sbjct: 2 GSNPKKEQMSGSEIISTEPATGAVLWRRPIGDVDAEVAAARASWADWAARPLTYRIEALR 61 Query: 71 LFGEVLREHKADLGELVSIEAGKITQEGLGEVQEMIDICDFAVGLSRQLYGLTIASERPG 130 F V+R+ +L++ E GK E EV+ +I D +V T SER G Sbjct: 62 RFANVVRQKSEAFTDLIARETGKPLWEARTEVETVIAKVDISV---------TAFSERTG 112 Query: 131 HHMRET---------WHPLGVVGVISAFNFPVAVWAWNTALALVAGNSVVWKPSEKTPLT 181 E P GV+ V+ +NFP + + AL+AGN+VV+KPSEKTP T Sbjct: 113 QRRIEAPMNTRLALRHKPHGVLAVLGPYNFPAHLPNGHIVPALLAGNAVVFKPSEKTPAT 172 Query: 182 ALACQALFEKALKAFGDAPAGLAQLVIGGREAGEAMVDDPRVPLVSATGSTRMGREVGPR 241 A + A G P G +L+IGG + G+A+ + + TGS R G + Sbjct: 173 G----AFLVECYHAAG-IPEGCIRLLIGGPDEGKALAGHDGIDGLLFTGSARTGIALNRA 227 Query: 242 VAARFGRSI-LELGGNNAMILAPSADLDLAVRGILFSAVGTAGQRCTTLRRLIVHRSIKD 300 AA+ + + LE+GGNN +++ + D+ A ++ SA +AGQRCT RRLIV + D Sbjct: 228 FAAKPEKILALEMGGNNPILVWSTPDIYSAAVLVIQSAFTSAGQRCTAARRLIVDEKLYD 287 Query: 301 EVVARVKAAYGKVRIGDPRKD--NLVGPLIDKQSFDAMQGALAKARDEGGQVFGGERQLA 358 ++ V G++ +G+P D +GP+ID + D + + + GG+ + Sbjct: 288 PLLEEVNKLIGRLIVGEPHADPAPFMGPVIDNDTADLLTESFLELSFMGGRPLRHMERPV 347 Query: 359 DQYPNAYYVSPAIAEMPAQSDVVRHETFAPILYVLAYDDFEEALRLNNEVPQGLSSCIFT 418 D P +++PA+ +M + E F PIL V+ FEEA+ N GLS+ + + Sbjct: 348 DGRP---FLTPAMIDMTDAKEKPDVELFGPILQVIRARTFEEAIAEANNTRYGLSASLVS 404 Query: 419 TDIREAERFQSASGSDCGIANVNIGTSGAEIGGAFGGEKETGGGRES 465 D + ++F + GI N N T+GA FGG +G R S Sbjct: 405 QDPKLYDQFW--ANIRAGIVNWNRPTNGASSAAPFGGIGWSGNHRPS 449 Lambda K H 0.318 0.135 0.396 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: 554 Number of extensions: 32 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: 496 Length of database: 480 Length adjustment: 34 Effective length of query: 462 Effective length of database: 446 Effective search space: 206052 Effective search space used: 206052 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 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