Align lactaldehyde dehydrogenase (EC 1.2.1.22); 2,5-dioxovalerate dehydrogenase (EC 1.2.1.26) (characterized)
to candidate WP_052600717.1 MICLODRAFT_RS27600 aldehyde dehydrogenase family protein
Query= BRENDA::Q97UA1 (478 letters) >NCBI__GCF_000262405.1:WP_052600717.1 Length = 491 Score = 352 bits (904), Expect = e-101 Identities = 187/472 (39%), Positives = 282/472 (59%), Gaps = 5/472 (1%) Query: 7 LADKWIKGSGEEYLDINPADKDHVLAKIRLYTKDDVKEAINKAVAKFDEWSRTPAPKRGS 66 +A +WI + E +INP++ + V+ + + + + AI A F WSR+ +R Sbjct: 6 IAGEWISAT-EASANINPSNTNDVVGEYARASAAEAERAIAAAYDAFPAWSRSSIQQRHD 64 Query: 67 ILLKAGELMEQEAQEFALLMTLEEGKTLKDSMFEVTRSYNLLKFYGALAFKISGKTLPSA 126 IL G+ + +E L++ EEGKTL + + EVTR+ + F+ +++G+ +PS Sbjct: 65 ILKAVGDEILARKEELGRLLSREEGKTLPEGIGEVTRAGQIFLFFSGECLRMAGEKVPSV 124 Query: 127 DPNTRIFTVKEPLGVVALITPWNFPLSIPVWKLAPALAAGNTAVIKPATKTPLMVAKLVE 186 P + +EP+GVV LITPWNFP++IP WK+APALA GNT V KPA P L E Sbjct: 125 RPFIDVEITREPVGVVGLITPWNFPIAIPAWKIAPALAYGNTVVFKPADLVPGSAHALSE 184 Query: 187 VLSKAGLPEGVVNLVVGKGSEVGDTIVSDDNIAAVSFTGSTEVGKRIYKLVGNKNRMTRI 246 ++ +AG+P GV NLV+G+GS VG+ ++ ++A+SFTGS G+++ + M ++ Sbjct: 185 IIIRAGVPAGVFNLVMGRGSVVGEAMLKSPKVSAISFTGSVPTGRKVAQTCITAEPMKKV 244 Query: 247 QLELGGKNALYVDKSADLTLAAELAVRGGFGLTGQSCTATSRLIINKDVYTQFKQRLLER 306 QLE+GGKN + V ADL +A E AV F TGQ CTA+SRLI+ + ++ +F + ER Sbjct: 245 QLEMGGKNPMVVLDDADLKVAVECAVNSAFFSTGQRCTASSRLIVTEGIHDRFVAAMQER 304 Query: 307 VKKWRVGPGTE-DVDMGPVVDEGQFKKDLEYIEYGKNVGAKLIYGGNII--PGKGYFLEP 363 ++ + + +GPVVD+ Q +DL+YI G+ GAKL+ GG ++ G++L P Sbjct: 305 MQGLVIDDALKAGTHIGPVVDQSQLDQDLKYIRIGQEEGAKLVAGGELLKRDAPGFYLAP 364 Query: 364 TIFEGVTSDMRLFKEEIFGPVLSVTEAKDLDEAIRLVNAVDYGHTAGIVASDIKAINEFV 423 +F V++ MR+ +EEIFGPV +VT AKD DEA+ L N +G ++GI + +K + F Sbjct: 365 ALFTEVSNQMRVAREEIFGPVATVTRAKDYDEALELANDTPFGLSSGICTTSLKYASHFK 424 Query: 424 SRVEAGVIKVNKPTVGLELQAPFGGFKNSGATTWKEMGEDALEFYLKEKTVY 475 EAG++ VN PT G++ PFGG K S +E G A EFY KT Y Sbjct: 425 RNAEAGMVMVNLPTAGVDYHVPFGGRKGSSYGP-REQGRYAEEFYTTVKTAY 475 Lambda K H 0.316 0.135 0.389 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: 618 Number of extensions: 25 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: 478 Length of database: 491 Length adjustment: 34 Effective length of query: 444 Effective length of database: 457 Effective search space: 202908 Effective search space used: 202908 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 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