Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_011830162.1 MPE_RS12990 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000015725.1:WP_011830162.1 Length = 477 Score = 289 bits (739), Expect = 2e-82 Identities = 183/490 (37%), Positives = 271/490 (55%), Gaps = 33/490 (6%) Query: 38 QIFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMD 97 + +I+ W D V K+ VNP+T +++ G DVD+AVKAAR AF + + + Sbjct: 6 KFYIDGHWVDPVKAKSLDVVNPATEASAGRISMGTAADVDRAVKAARKAF---ASYSQTS 62 Query: 98 ASHRGRLLNRLADLIERDRTY--LAALETLDNGKPYVISY-------LVDLDMVLKCLRY 148 + R LL R+ ++E + Y +AA T + G P +S + L + L L+ Sbjct: 63 VAERASLLERI--IVEYKKRYADMAAAITEEMGAPVALSKDAQAAMGIAHLQIALDVLKN 120 Query: 149 YAGWADKYHGKTIPIDGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVM 208 Y + T+ + EP+GVCG I PWN+P+ A K+ PALA G +V+ Sbjct: 121 YK--FQELRDTTLMVK---------EPIGVCGFITPWNWPVNQIACKVAPALAVGCTMVL 169 Query: 209 KVAEQTPLTALYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGR 268 K +E P +A ++ AG P GV N+V G GPT GAA++SH DVD V+FTGST G Sbjct: 170 KPSEIAPFSAYLWTEILHAAGVPAGVFNLVNGDGPTVGAALSSHPDVDMVSFTGSTRAG- 228 Query: 269 VIQVAAGSS-NLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFV 327 ++VA ++ +KRV ELGGKSPNII+ DAD A+ + N GQ C A +R V Sbjct: 229 -VEVARNAAPTVKRVHQELGGKSPNIILPDADFKHAITAGVQGVMLNSGQSCNAPTRMLV 287 Query: 328 QEDIYDEFVERSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCG 387 DE + + A++ VG+P S GP + TQ+ KI I+ G +EGA ++ G Sbjct: 288 PNARLDEALAIAKEAAEATTVGDP-ASGAALGPVISATQWDKIQTLIHKGIEEGATVVAG 346 Query: 388 G---GIAADRGYFIQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGL 444 G + GY+++PTV G V + MT+A+EEIFGPV+ IL + T+++ V N++ YGL Sbjct: 347 GPGKPKGLETGYYVKPTVLGHVNNQMTVAREEIFGPVLTILGYDTVDQAVEIGNDTPYGL 406 Query: 445 AAAVFTKDLDKANYLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTE 504 AA V D + ++ L+AG V +N + ++PFGG+K SG+GRE G++ + E Sbjct: 407 AAYVSGTDPEATRKVASRLRAGQVNINSVPL-DFKAPFGGFKQSGNGREWGDHAFGEFLE 465 Query: 505 VKTVTVKVPQ 514 VK V P+ Sbjct: 466 VKAVLGYAPK 475 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: 585 Number of extensions: 27 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: 477 Length adjustment: 34 Effective length of query: 483 Effective length of database: 443 Effective search space: 213969 Effective search space used: 213969 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 Sep 24 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:
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