Align Putative aldehyde dehydrogenase transmembrane protein; EC 1.2.1.3 (characterized, see rationale)
to candidate Ga0059261_1680 Ga0059261_1680 NAD-dependent aldehyde dehydrogenases
Query= uniprot:Q92L07 (510 letters) >FitnessBrowser__Korea:Ga0059261_1680 Length = 469 Score = 211 bits (538), Expect = 4e-59 Identities = 151/468 (32%), Positives = 217/468 (46%), Gaps = 17/468 (3%) Query: 25 KDLYTGGDMPSFSPVTGEKIASLKTVSAAEAAGKIEKADEAFRAWRLVPAPKRGELVRLL 84 K L P P TG A S A+ + A AF W P R + + Sbjct: 11 KPLAMAETFPVIDPATGRPFADAPLASTADLDAAVAAARRAFPGWAATPIEDRAAAILAI 70 Query: 85 GEELRAFKADLGRLVSIEAGKIPSEGLGEVQEMIDICDFAVGLSRQLYGLTIATERPGHR 144 + + A K +L RL+S E GK +GE+ + GL + + + R Sbjct: 71 ADSIEAAKDELARLLSAEQGKPVPNAVGEIMGALAWARATAGLRP---AVDVLKDDDSVR 127 Query: 145 MMETWHPLGVVGIISAFNFPVAVWSWNAALALVCGDAVVWKPSEKTPLTALACQAILERA 204 + PLGVV IS +NFPV + W+ LV G+ VV KPS TPL AL I Sbjct: 128 VEVHRKPLGVVASISPWNFPVMIAIWHIIPGLVAGNTVVMKPSSFTPLAALRMVEIANAH 187 Query: 205 IARFGDAPEGLSQVLIGDRAIGEVLVDHPKVPLVSATGSTRMGREVGPRLAKRFARAILE 264 + P G+ + G+ IG + HP + + TGST GR + A R LE Sbjct: 188 L------PPGVLNSVTGEVEIGRAIASHPGIDKIVFTGSTPTGRSIMADGAANLKRLTLE 241 Query: 265 LGGNNAGIVCPSADLDMALRAIAFGAMGTAGQRCTTLRRLFVHESVYDQLVPRLKKAYQS 324 LGGN+A IV P AD+D I A G +GQ C ++R++VHES++D L +L + ++ Sbjct: 242 LGGNDAAIVLPDADVDKVAAKIFAKAFGNSGQICAAVKRVYVHESIHDALAEKLAEMART 301 Query: 325 VSVGNPLESAALVGPLVDKAAFDGMQKAIAEAKNHGGAVTGGERVELGHENGYYVKPALV 384 VG ++A+ GP+ ++ FD ++ +A+ HGG G G +GY+ P V Sbjct: 302 AVVGPGSDAASQFGPVQNRKQFDLVRALADDARAHGGRFLAGGEAREG--DGYFF-PLSV 358 Query: 385 EMPKQEGP--VLEETFAPILYVMKYSDFDAVLAEHNAVAAGLSSSIFTRDMQESERFLAA 442 + +G V EE F PIL V++YSD + LA NA GL S+++ D + F A Sbjct: 359 VVDVTDGMRIVDEEQFGPILPVIRYSDPEDALARANANENGLGGSVWSADPAAALAF--A 416 Query: 443 DGSDCGIANVNIGTSGAEIGGAFGGEKETGGGRESGSDAWKAYMRRAT 490 + G VN S FGG K++G G E G + YM+ T Sbjct: 417 QRLEAGTVWVNDHAS-ISPDVPFGGAKQSGVGTEFGLYGLEEYMQLQT 463 Lambda K H 0.317 0.134 0.390 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: 577 Number of extensions: 25 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: 510 Length of database: 469 Length adjustment: 34 Effective length of query: 476 Effective length of database: 435 Effective search space: 207060 Effective search space used: 207060 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