Align Aldehyde dehydrogenase family 7 member A1; Antiquitin-1; Matured fruit 60 kDa protein; MF-60; EC 1.2.1.3 (characterized)
to candidate RR42_RS18500 RR42_RS18500 aldehyde dehydrogenase
Query= SwissProt::Q9ZPB7 (508 letters) >FitnessBrowser__Cup4G11:RR42_RS18500 Length = 492 Score = 436 bits (1120), Expect = e-126 Identities = 226/472 (47%), Positives = 303/472 (64%), Gaps = 4/472 (0%) Query: 40 SPSNNQEIAKVTEVSMEEYEEGLRSCNDAAKTWKSLPAPKRGEIVRQIGDALREKLQHLG 99 SP + + + S+ E + + +W +PAP RGE+VR+ G+ LRE +HLG Sbjct: 19 SPIDGEAFGHLPACSLAEADARIERARVMQASWALVPAPVRGEVVRRFGEVLREHKKHLG 78 Query: 100 KLVSLEMGKILAEGIGEVQEVIYMCDFAVGLSRQLNGSIIPSERPDHMMFEVWNPLGIVG 159 +LVSLE GKIL EG+GEVQE+I +CDFAVGLSRQL+G I SERP H M E W+P G+ G Sbjct: 79 ELVSLEAGKILQEGLGEVQEMIDICDFAVGLSRQLHGLTIASERPQHAMRETWHPYGLCG 138 Query: 160 VITAFNFPCAVLGWNACIALVCGNCVVWKGAPTTPLVTIAVTKLIAEVLE-KNNLPAAIF 218 VI+AFNFP AV WNA +ALVCGN V+WK + TPL +A+ L+ VLE I Sbjct: 139 VISAFNFPVAVWAWNAALALVCGNGVIWKPSEKTPLTALAMQSLLDGVLEIAAPQHVGIA 198 Query: 219 TAFCGGAEIGEAIAKDTRIPLVSFTGSSKVGAKVQQIVTERFGKCLLELSGNNALIVMDD 278 T GG +G+ + + + LVS TGS+++G V ERF + +LEL GNNA I+ Sbjct: 199 TVLSGGPALGQHLVEHAAVRLVSATGSTRMGRAVGIACAERFKRAILELGGNNAAIIAPS 258 Query: 279 ADVGLAVRSIFFAAVGTAGQRCTTCRRLYLHESIYQNVLDKLVGLYNQVKIGDPLEEGTL 338 AD+ LAVR++ F+A GTAGQRCT+ RR ++H + + V +L+ ++ ++ +GDPL E TL Sbjct: 259 ADLELAVRAMTFSAAGTAGQRCTSLRRAFVHVDVLEAVTTRLIQVFGRLPVGDPLAETTL 318 Query: 339 VGPVHTKASRENFEKGISTIKSQGGKILTGGSVIES---DGNFVQPTIVEIASNASVVKE 395 VGP+ A+ + + G + G V+ + +V+P +V + Sbjct: 319 VGPLIDGAAGAAMAAALLRCREHGNTVHGGERVLAEKYPNAEYVRPALVLTDRQHETMLS 378 Query: 396 ELFGPVLYVMKFKTLEEAIALNNSVPQGLSSSIFTSKPNTIFKWIGPHGSDCGIVNVNIP 455 E F P+LYVM + TL+EAIALNN+ GLSS IFT +++ GSDCGI NVNI Sbjct: 379 ETFAPILYVMPYTTLDEAIALNNASEHGLSSCIFTESLREAERFMSASGSDCGIANVNIG 438 Query: 456 TNGAEIGGAFGGEKATGGGREAGSDSWKQYMRRSTCTINYGTELPLAQGINF 507 T+GAEIGGAFGGEKATGGGRE+GSD+WK YMRR+T T+NYG LPLAQG+ F Sbjct: 439 TSGAEIGGAFGGEKATGGGRESGSDAWKGYMRRATNTVNYGDALPLAQGVRF 490 Lambda K H 0.317 0.136 0.404 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: 731 Number of extensions: 32 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: 508 Length of database: 492 Length adjustment: 34 Effective length of query: 474 Effective length of database: 458 Effective search space: 217092 Effective search space used: 217092 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: 52 (24.6 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:
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