Align lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate Ga0059261_0516 Ga0059261_0516 vanillin dehydrogenase (EC 1.2.1.67)
Query= BRENDA::Q58806 (463 letters) >FitnessBrowser__Korea:Ga0059261_0516 Length = 478 Score = 220 bits (561), Expect = 7e-62 Identities = 148/456 (32%), Positives = 238/456 (52%), Gaps = 12/456 (2%) Query: 16 INPYSLEVIKKIPALSREEAKEAIDTAEKYKEVMKNLPITKRYNILMNIAKQIKEKKEEL 75 +NP + EV + A + ++A EA++ A L R L A+ + K E+ Sbjct: 16 LNPVTGEVATEAQAFTVDQANEAVEAAAAAFPAWSTLGPNARRAALNKAAEALAAKAEDF 75 Query: 76 AKILAIDAGKPIKQARVEVERSIGTFKLAAFYVKEHRDEVIPSDDR--LIFTRREPVGIV 133 + + + G AR + ++ + AA + EVIPSD + REPVG++ Sbjct: 76 VEAMNGEIGATEGWARFNLMLAVSMVREAAALTTQIGGEVIPSDKPGCIAMAIREPVGVM 135 Query: 134 GAITPFNFPLNLSAHKIAPAIATGNVIVHHPSSKAPLVCIELAKIIENALKKYNVPLGVY 193 I P+N P+ L +A +A GN +V S + P +A+ + AL K V + V Sbjct: 136 LGIAPWNAPIILGVRAVAAPLACGNTVVLKASEQCPRTHSLIAEAFDEALPKGAVSI-VT 194 Query: 194 NLLTGAGEVVGDEIVVNEKVNMISFTGSSKVGELITKKAG--FKKIALELGGVNPNIVLK 251 N A E+VG ++ N + I+FTGS+ VG +I K+A K + LELGG P +VL+ Sbjct: 195 NAPEDAPEIVG-ALIDNPHIRRINFTGSTAVGRIIAKRAAEHLKPVLLELGGKAPMLVLE 253 Query: 252 DADLNKAVNALIKGSFIYAGQVCISVGMILVDESIADKFIEMFVNKAKVLNVGNPLDEKT 311 DADL++AV A G+F+ GQ+C+S I+V +++AD F+E F K + VG+P + KT Sbjct: 254 DADLDEAVKAAAFGAFMNQGQICMSTERIIVVDAVADAFVEKFAAKVGTMPVGDPREGKT 313 Query: 312 DVGPLISVEHAEWVEKVVEKAIDEGGKLLLGG---KRDKALFYP--TILEVDRDNILCKT 366 +G ++ + V+ ++ A+ G + GG + + P I V D L + Sbjct: 314 PLGAVVDQKTVAHVKALIGDALAAGAVQVNGGGVLEGTGGVLMPAHVIDHVTPDMKLFRD 373 Query: 367 ETFAPVIPIIRTNEE-EMIDIANSTEYGLHSAIFTNDINKSLKFAENLEFGGVVINDSSL 425 E+F PV+ +IR +E I +AN TEYGL +++FT D + L+ A ++ G +N ++ Sbjct: 374 ESFGPVVGVIRARDEAHAILLANDTEYGLSASVFTRDTARGLRVARQIKSGICHVNGPTV 433 Query: 426 FRQDNMPFGGVKKSGLGREGVKYAMEEMSNIKTIII 461 + MPFGGVK SG GR G K ++ + ++ I I Sbjct: 434 HDEAQMPFGGVKASGYGRFGGKAGIDAFTELRWITI 469 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: 482 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: 478 Length adjustment: 33 Effective length of query: 430 Effective length of database: 445 Effective search space: 191350 Effective search space used: 191350 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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