Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_015928270.1 MNOD_RS07620 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000022085.1:WP_015928270.1 Length = 506 Score = 382 bits (980), Expect = e-110 Identities = 221/489 (45%), Positives = 288/489 (58%), Gaps = 22/489 (4%) Query: 40 FINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMDAS 99 FI +W + F +P TG VIC+VA D +D+++A+ AA AA + W + Sbjct: 22 FIGGQWVAPAGGRYFENTSPLTGRVICEVARSDAQDIERALDAAHAAKEA---WGHTAPA 78 Query: 100 HRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYHGK 159 R R+LNR+AD +E + LA ET DNGKP + D+ + + RY+AG G Sbjct: 79 ERARILNRMADRMEENLELLALAETWDNGKPIRETTHADIPLAIDHFRYFAGCIRAQEGS 138 Query: 160 TIPIDGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLTAL 219 ID D +Y HEP+GV GQIIPWNFPLLM WKL PALA GN VV+K AEQTP + L Sbjct: 139 LSEIDQDTVAYHFHEPLGVVGQIIPWNFPLLMAVWKLAPALAAGNCVVLKPAEQTPASVL 198 Query: 220 YVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSSNL 279 +A ++ + P GV+NIV GFG AG +AS + K+AFTG T GR+I A S NL Sbjct: 199 VLAEIVGDL-LPAGVLNIVNGFGLEAGKPLASSPRIAKIAFTGETSTGRLIMQYA-SQNL 256 Query: 280 KRVTLELGGKSPNIIM------SDADMDWAVEQAHFALF-FNQGQCCCAGSRTFVQEDIY 332 VTLELGGKSPNI DA +D A+E F +F NQG+ C SR V E IY Sbjct: 257 IPVTLELGGKSPNIFFKDVLAEDDAFLDKALE--GFTMFALNQGEVCTCPSRALVHEAIY 314 Query: 333 DEFVERSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGG---- 388 D F+E++VAR + G+P D T G Q Q +KIL YI+ GKQEGA+LL GG Sbjct: 315 DRFIEKAVARVNAIKQGSPLDPATMIGAQASGEQLQKILSYIDIGKQEGAQLLTGGERNR 374 Query: 389 --GIAADRGYFIQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAA 446 G A +G++++PTVF + M I +EEIFGPV+ + FK EE + AN++ YGL A Sbjct: 375 LEGEFA-QGFYVKPTVFKG-HNRMRIFQEEIFGPVLSVTTFKDDEEALAIANDTLYGLGA 432 Query: 447 AVFTKDLDKANYLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTEVK 506 V+T+D+ +A +A+QAG VW NCY + A + FGGYK SG GRE L Y + K Sbjct: 433 GVWTRDITRAYRFGRAIQAGRVWTNCYHAYPAHAAFGGYKQSGIGRENHRMMLDHYQQTK 492 Query: 507 TVTVKVPQK 515 + V K Sbjct: 493 NMLVSYSPK 501 Lambda K H 0.319 0.136 0.409 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: 595 Number of extensions: 23 Number of successful extensions: 6 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: 517 Length of database: 506 Length adjustment: 35 Effective length of query: 482 Effective length of database: 471 Effective search space: 227022 Effective search space used: 227022 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: 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