Align Geranial dehydrogenase; GaDH; Geraniol oxidation pathway protein B; EC 1.2.1.86 (characterized)
to candidate WP_076948594.1 C1M55_RS05435 aldehyde dehydrogenase
Query= SwissProt::H1ZV37 (478 letters) >NCBI__GCF_002893965.1:WP_076948594.1 Length = 481 Score = 419 bits (1078), Expect = e-122 Identities = 222/475 (46%), Positives = 308/475 (64%), Gaps = 4/475 (0%) Query: 4 DHQHIFVGGQWIAPKSTQRSNILNASTEELVGSVPKCNNEDMDRAVAAAREAMRSLAWAG 63 D+ +++GG W+AP + Q + + +TEE VGS P ++D AV+AAR A W+ Sbjct: 3 DYDKLYIGGAWVAPATDQVLEVFSPATEERVGSCPIAAPANIDAAVSAARAAFEG-PWSR 61 Query: 64 LDGKGRAQHLRRFADAVERRGQQLARSVSLQNGMPINVADQLESAFVVSLLRYYASLAEN 123 R L + A +E R ++ + +S + G P + ++ ++ L YYA LA+ Sbjct: 62 TTPAERGAILAKAAKLIEERSAEINQLISNEMGQPPAMVGMMQQTPSMATLGYYAELADK 121 Query: 124 LVEEEARPSPTGSTTLVRRDPVGVVGAIIPWNFPVALSIFKIAPALAAGCAVVVKPSSGT 183 EE R G T V R+PVGVV A++ WN P+ L+I K+APAL AGC V++KP+ + Sbjct: 122 FAWEEKRTGAFGQTK-VTREPVGVVAAVLAWNVPLFLAINKLAPALLAGCTVLLKPAPES 180 Query: 184 VLDSYVLAEAAAEAGLPPGVINWVPGDRGIGSHLVSHPGVDKVAFTGSTSAGRIIAEACA 243 L +V+AE EAG+P GVI+ +PG G +LVSH G+DK+ FTGS++ GR I A Sbjct: 181 PLSVHVIAEIFTEAGVPEGVISVLPGGAETGEYLVSHAGIDKITFTGSSAVGRKIGAIAA 240 Query: 244 RLLRPVTLELGGKSAAIVLEDADLDALIRSLPMSSVLNNGQACFSCTRILAPAGRYDEVV 303 + L+ +LELGGKSAAI+LEDAD+ A + L MS ++N GQAC + TRILAP RYDEV+ Sbjct: 241 QNLKRCSLELGGKSAAIILEDADIAAGMPMLVMSGLMNTGQACVAQTRILAPRSRYDEVI 300 Query: 304 DAIAGAVSAYSVGDALDRATVVGPMASAAHRDSVQRYIELGTGE-ARLVVGGGR-TSQDR 361 + + A +VGD D A +GP+ S R+ V+ YI G E AR+V+GGGR D+ Sbjct: 301 EGMKTAAGFMTVGDPSDPAAQLGPLISEKQRERVEGYIAKGKEEGARVVLGGGRPAGLDK 360 Query: 362 GWFVQPTVFADVDNRSRIAREEIFGPVLSIIRYEGEDEAVEIANDSEYGLGGTVWSTDHD 421 GW+V+PT+FADVDN IAREEIFGPVLS+I Y+ EDEA++IANDS+YGL G+VW+TD D Sbjct: 361 GWYVEPTIFADVDNSMTIAREEIFGPVLSVIPYDSEDEAIKIANDSDYGLAGSVWTTDID 420 Query: 422 HAVTIARRMETGTVGINGYMPDLNAPFGGVKSSGMGRELGPESIGAYQRYKSVYL 476 H + +A ++ TGT IN Y D +PFGG K+SG+GRE GPE + A+ KSV + Sbjct: 421 HGLEVAAQIRTGTYAINWYAFDPGSPFGGYKNSGIGRENGPEGLEAFCETKSVLM 475 Lambda K H 0.317 0.134 0.391 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: 614 Number of extensions: 19 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: 481 Length adjustment: 34 Effective length of query: 444 Effective length of database: 447 Effective search space: 198468 Effective search space used: 198468 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 (21.7 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