Align lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_076581509.1 BB347_RS11295 aldehyde dehydrogenase family protein
Query= BRENDA::Q58806 (463 letters) >NCBI__GCF_001971705.1:WP_076581509.1 Length = 497 Score = 277 bits (708), Expect = 7e-79 Identities = 158/482 (32%), Positives = 276/482 (57%), Gaps = 25/482 (5%) Query: 1 MFIDGKWINREDMDVI---NPYSLEVIKKIPALSREEAKEAIDTAEKYKEVMKNLPITKR 57 +++ G+W +D + I NP++ E I +PA + ++ +A + A + + P R Sbjct: 15 LYLAGEWTEPDDRETITVENPFTREEIATVPAGTEDDVDQAYERAAAAQREWADQPPQAR 74 Query: 58 YNILMNIAKQIKEKKEELAKILAIDAGKPIKQARVEVERSIGTFKLAAFYV----KEHRD 113 ++ + +++ +EE+ ++LA+++G + E++ + G + AA Y H+ Sbjct: 75 AGVITAALEFVQDHREEITELLALESGSTQVKCGAELQTATGMMQQAASYPFRMDGSHKG 134 Query: 114 EVIPSDDRLIFTRREPVGIVGAITPFNFPLNLSAHKIAPAIATGNVIVHHPSSKAPLVC- 172 IP + ++ R+P G+VG I+P+NFPL+LS +APA+ATGN +V P+S P+ Sbjct: 135 STIPGKENVV--ERQPAGVVGVISPWNFPLHLSMRAVAPALATGNAVVLKPASNTPISGG 192 Query: 173 IELAKIIENALKKYNVPLGVYNLLTGAGEVVGDEIVVNEKVNMISFTGSSKVGELITKKA 232 + LA+I E A VP GV +++TG G VGD + ++ +++FTGS+++G+ + A Sbjct: 193 LLLARIFEEA----GVPEGVLSVVTGRGSAVGDAVSDHDVPRVLAFTGSTEIGQHVAANA 248 Query: 233 GFKKI--ALELGGVNPNIVLKDADLNKAVNALIKGSFIYAGQVCISVGMILVDESIADKF 290 ALELGG N ++V ++ADL +AV+ + GSF++ GQ CIS+ LV E + D++ Sbjct: 249 AGNCALPALELGGNNVHVVTENADLERAVDGGVFGSFLHQGQACISINRHLVHEDVYDEY 308 Query: 291 IEMFVNKAKVLNVGNPLDEKTDVGPLISVEHAEWVEKVVEKAIDEGGKLLLGG------- 343 ++ ++A L G+P DE+T +GP+I + + + VE+ +DEG L GG Sbjct: 309 VDALADRAASLPSGDPTDEETVIGPIIDESQRDQILEYVEETVDEGATLETGGGAANIDE 368 Query: 344 KRDKALFYPTIL-EVDRDNILCKTETFAPVIPII-RTNEEEMIDIANSTEYGLHSAIFTN 401 D + PT+L E D D E F PV P I +++EE I++AN T +GL ++ + Sbjct: 369 VADSLVVEPTVLSEADNDMAAACNEHFGPVAPAIPYSSDEEAIELANETIHGLSGSVHSE 428 Query: 402 DINKSLKFAENLEFGGVVINDSSLFRQDNMPFGGVKKSGLGREGVKYAMEEMSNIKTIII 461 D+ ++ + A+ +E G + IND + + ++PFGG+K+SGLGR +EE++ K I I Sbjct: 429 DLAQARRIADGIETGMIHINDQPINDEPHVPFGGMKQSGLGRYNADSILEELTTTKWISI 488 Query: 462 SK 463 + Sbjct: 489 QR 490 Lambda K H 0.317 0.137 0.381 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: 532 Number of extensions: 24 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: 463 Length of database: 497 Length adjustment: 34 Effective length of query: 429 Effective length of database: 463 Effective search space: 198627 Effective search space used: 198627 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 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