Align lactaldehyde dehydrogenase (EC 1.2.1.22); 2,5-dioxovalerate dehydrogenase (EC 1.2.1.26) (characterized)
to candidate WP_179243903.1 B9O00_RS00790 aldehyde dehydrogenase family protein
Query= BRENDA::Q97UA1 (478 letters) >NCBI__GCF_900177295.1:WP_179243903.1 Length = 480 Score = 350 bits (899), Expect = e-101 Identities = 194/475 (40%), Positives = 278/475 (58%), Gaps = 11/475 (2%) Query: 7 LADKWIKGSGEEYLDINPADKDHVLAKIRLYTKDDVKEA---INKAVAKFDEWSRTPAPK 63 +A +W+ + NP+D V+ LY + D +A I+ A A F WSR+ + Sbjct: 8 IAGEWVDAPNASE-NRNPSDLSDVVG---LYAQGDAAQAGQAIDAAAAAFPAWSRSTPQQ 63 Query: 64 RGSILLKAGELMEQEAQEFALLMTLEEGKTLKDSMFEVTRSYNLLKFYGALAFKISGKTL 123 R IL AG + +E L++ EEGKTL + + E R+ + KF+ A +I+G + Sbjct: 64 RFDILDAAGTEILARKEELGRLLSREEGKTLPEGIGETVRAGQIFKFFAGEALRIAGDRI 123 Query: 124 PSADPNTRIFTVKEPLGVVALITPWNFPLSIPVWKLAPALAAGNTAVIKPATKTPLMVAK 183 S P +EPLGVV LITPWNFP++IP WKLAPALA GN V+KPA P Sbjct: 124 DSTRPGVIAEATREPLGVVGLITPWNFPIAIPAWKLAPALAFGNCVVMKPADLVPGCAWA 183 Query: 184 LVEVLSKAGLPEGVVNLVVGKGSEVGDTIVSDDNIAAVSFTGSTEVGKRIYKLVGNKNRM 243 L ++L +AGLP+GV NLV+G+GS VG+ I++ +AA+SFTGS G+ + + M Sbjct: 184 LADILQRAGLPKGVFNLVMGRGSVVGEAILASPKVAAISFTGSVATGRHVARRCIEGEAM 243 Query: 244 TRIQLELGGKNALYVDKSADLTLAAELAVRGGFGLTGQSCTATSRLIINKDVYTQFKQRL 303 + QLE+GGKN V ADL +AA A+ G F TGQ CTA+SRLI+ + ++ +F + L Sbjct: 244 KKFQLEMGGKNPFVVLDDADLEVAANSALNGAFFSTGQRCTASSRLIVTEGIHDRFVEAL 303 Query: 304 LERVKKWRVGPG-TEDVDMGPVVDEGQFKKDLEYIEYGKNVGAKLIYGGNII--PGKGYF 360 ++K +V E +GPVVD+ Q +DL+YI+ G++ GAKL +GG + +G++ Sbjct: 304 TSKLKALKVDNALKEGTQIGPVVDQRQLDQDLDYIKVGQDEGAKLAWGGERLNRETEGFY 363 Query: 361 LEPTIFEGVTSDMRLFKEEIFGPVLSVTEAKDLDEAIRLVNAVDYGHTAGIVASDIKAIN 420 L+P +F + MR+ +EEIFGPV SV KD D A+ + N +G +AGI S +K Sbjct: 364 LQPALFTETDNAMRINREEIFGPVASVIRVKDYDSALAVANDTQFGLSAGIATSSLKHAE 423 Query: 421 EFVSRVEAGVIKVNKPTVGLELQAPFGGFKNSGATTWKEMGEDALEFYLKEKTVY 475 F +AG++ VN PT G++ PFGG KNS +E G A+EFY KT Y Sbjct: 424 HFKRNSQAGMVMVNLPTAGVDYHVPFGGRKNSSYGA-REQGRYAVEFYTTVKTAY 477 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: 583 Number of extensions: 26 Number of successful extensions: 4 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: 480 Length adjustment: 34 Effective length of query: 444 Effective length of database: 446 Effective search space: 198024 Effective search space used: 198024 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: 51 (24.3 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