Align Putative aldehyde dehydrogenase AldY; EC 1.2.1.3 (characterized)
to candidate WP_058932630.1 AU252_RS22680 aldehyde dehydrogenase family protein
Query= SwissProt::P94358 (485 letters) >NCBI__GCF_001484605.1:WP_058932630.1 Length = 491 Score = 437 bits (1125), Expect = e-127 Identities = 214/475 (45%), Positives = 320/475 (67%), Gaps = 3/475 (0%) Query: 6 LNKSFINGKWTGGESGRTEDILNPYDQSVITTASLATGKQLEDAFDIAQKAQKEWAKSTT 65 + + FI G W G S +T + NPYD SV+ + A + L++A+ A+ AQKEWA Sbjct: 17 VTQQFIGGTWREGRSEKTLTVTNPYDDSVLASIRQANKQDLDEAYRAAEAAQKEWAAQPP 76 Query: 66 EDRKAVLQKARGYLHENRDDIIMMIARETGGTIIKSTIELEQTIAILDEAMTYTGELGGV 125 R+ V+ +A L E R++I+ + +E+G T+ K+ +E+ I EA ++ + G Sbjct: 77 AARRQVILRAAQILEERREEIVDWLIKESGSTVGKAQVEVSLAAGITLEASSFPTRVHG- 135 Query: 126 KEVPSDIEGKTNKIYRLPLGVISSISPFNFPMNLSMRSIAPAIALGNSVVHKPDIQTAIS 185 + V S+ GK +IYR P+GV+ ISP+NFP++LS RS+APA+ALGN+VV KP T ++ Sbjct: 136 RIVESNTPGKELRIYRRPIGVVGVISPWNFPLHLSERSVAPALALGNAVVIKPASDTPVT 195 Query: 186 GGTIIAKAFEHAGLPAGVLNVMLTDVKEIGDGMLTNPIPRLISFTGSTAVGRHIGEIA-- 243 GG I+A+ FE AGLP GVLNV++ EIGD +T+P+P LISFTGST +G+++G++A Sbjct: 196 GGLILARVFEEAGLPPGVLNVVVGAGSEIGDDFVTHPVPGLISFTGSTPIGKNVGKLAAG 255 Query: 244 GRAFKRMALELGGNNPFAVLSDADVDRAVDAAIFGKFIHQGQICMIINRIIVHQDVYDEF 303 G+ K +ALELGGN P VL+DA++D AV+AA+ GKF+HQGQICM +NRIIV +YDEF Sbjct: 256 GKHLKHVALELGGNAPLVVLADANLDAAVEAAVLGKFLHQGQICMAVNRIIVEAPLYDEF 315 Query: 304 VEKFTARVKQLPYGDQTDPKTVVGPLINERQIEKALEIIEQAKTDGIELAVEGKRVGNVL 363 VE+FTA +P+GD +T+VGP++N+ Q+E I AK +G +EG+ G V+ Sbjct: 316 VERFTAAASGVPFGDPASAQTLVGPVVNDSQLEGLKTKIATAKAEGARTVLEGEITGRVV 375 Query: 364 TPYVFVGADNNSKIAQTELFAPIATIIKAGSDQEAIDMANDTEYGLSSAVFTSDLEKGEK 423 P+VF +++IA+ E+F P+ IIKA ++ A+++AN TE+GLSS+VFT DL++G + Sbjct: 376 PPHVFADVSPDTEIAREEIFGPLVGIIKANNEAHALELANATEFGLSSSVFTQDLDRGVQ 435 Query: 424 FALQIDSGMTHVNDQSVNDSPNIAFGGNKASGVGRFGNPWVVEEFTVTKWISIQK 478 F+L I +GMTH+N+ V+D ++ FGG SG+GRF W + EFT + +++ Sbjct: 436 FSLGIKAGMTHINEMPVHDESHVPFGGEGNSGLGRFNGDWAIAEFTTDHTVGVKR 490 Lambda K H 0.316 0.134 0.380 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: 664 Number of extensions: 22 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: 485 Length of database: 491 Length adjustment: 34 Effective length of query: 451 Effective length of database: 457 Effective search space: 206107 Effective search space used: 206107 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 (21.6 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