Align Geranial dehydrogenase; GaDH; Geraniol oxidation pathway protein B; EC 1.2.1.86 (characterized)
to candidate WP_034269044.1 AMYHA_RS06610 aldehyde dehydrogenase
Query= SwissProt::H1ZV37 (478 letters) >NCBI__GCF_000504245.1:WP_034269044.1 Length = 481 Score = 463 bits (1191), Expect = e-135 Identities = 236/476 (49%), Positives = 318/476 (66%), Gaps = 3/476 (0%) Query: 4 DHQHIFVGGQWIAPKSTQRSNILNASTEELVGSVPKCNNEDMDRAVAAAREAMRSLAWAG 63 +++ +++GG W+AP++ ++ +++ +E+LVG P+ D+DRAV AAR A W Sbjct: 3 EYKELYIGGSWVAPETERQIEVISPHSEQLVGRTPEATTADVDRAVEAARRAFDHGDWPN 62 Query: 64 LDGKGRAQHLRRFADAVERRGQQLARSVSLQNGMPINVADQLESAFVVSLLRYYASLAEN 123 + R LRRFADA R +LA S + G P+ + + L + ++ E Sbjct: 63 TAPEDRLAALRRFADAYNARQAELAELFSTEMGSPLWFSQVGQVGATSMALGEFLNIGEQ 122 Query: 124 LVEEEARPSPTGSTTLVRRDPVGVVGAIIPWNFPVALSIFKIAPALAAGCAVVVKPSSGT 183 + EE R G +VRR+PVGVVG I PWN P +++ K+ PAL AGC VV+KP Sbjct: 123 IAWEERRTGSFGGEVVVRREPVGVVGVITPWNVPHFVTMAKLVPALLAGCTVVLKPPPEA 182 Query: 184 VLDSYVLAEAAAEAGLPPGVINWVPGDRGIGSHLVSHPGVDKVAFTGSTSAGRIIAEACA 243 L + VLAE AEAGLP GV++ VP R +G HLV+HP VDK+AFTGST+AGR IA C Sbjct: 183 PLSALVLAEIVAEAGLPEGVVSVVPAGREVGEHLVTHPDVDKIAFTGSTAAGRRIAALCG 242 Query: 244 RLLRPVTLELGGKSAAIVLEDADLDALIRSLPMSSVLNNGQACFSCTRILAPAGRYDEVV 303 + LR VTLELGGKSAA++L+DADL ++ L M+S+LN+GQAC + TRILA RYDEVV Sbjct: 243 QDLRRVTLELGGKSAAVILDDADLGQTVQQLQMASLLNSGQACIAQTRILASRKRYDEVV 302 Query: 304 DAIAGAVSAYSVGDALDRATVVGPMASAAHRDSVQRYIELGTGE-ARLVVGGGR--TSQD 360 DA+A V +VGD ++ +GPM + ++ ++ YI +GT E ARLV+GG D Sbjct: 303 DALAAMVGGLTVGDPMNVENYIGPMVAKRQQERIRDYIGIGTAEGARLVIGGSEMPAGLD 362 Query: 361 RGWFVQPTVFADVDNRSRIAREEIFGPVLSIIRYEGEDEAVEIANDSEYGLGGTVWSTDH 420 GW++QPTVFADVDN RIAREEIFGPVL++I Y+ E +AV IANDSEYGL G+VW++D Sbjct: 363 TGWYIQPTVFADVDNGMRIAREEIFGPVLTVIPYDDEADAVRIANDSEYGLAGSVWTSDV 422 Query: 421 DHAVTIARRMETGTVGINGYMPDLNAPFGGVKSSGMGRELGPESIGAYQRYKSVYL 476 +H + +AR++ TGT+GIN Y+ D APFGG K+SG+GRE GPE I Y YKSV L Sbjct: 423 EHGLDVARQVRTGTLGINQYLMDFAAPFGGFKASGIGREFGPEGIEPYVEYKSVAL 478 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: 646 Number of extensions: 23 Number of successful extensions: 3 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