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 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