Align predicted periplasmic glycoside 3-dehydrogenase (EC 1.1.99.13) (characterized)
to candidate CA265_RS23295 CA265_RS23295 oxidoreductase
Query= reanno::Btheta:351686 (491 letters) >FitnessBrowser__Pedo557:CA265_RS23295 Length = 484 Score = 321 bits (822), Expect = 4e-92 Identities = 190/478 (39%), Positives = 261/478 (54%), Gaps = 39/478 (8%) Query: 5 SRRKFLKTGAAALAGITIAPSSILGMSHGHVSPTDKLNLAAVGIGGMGHANINNVK--GT 62 SRR F+KT A A AG I P +LG G ++P+D+L LA +G GG G ++I ++ G Sbjct: 13 SRRNFIKTTALAAAGFMIVPRHVLG-GPGFLAPSDRLQLAGIGAGGKGESDIASIVRGGK 71 Query: 63 ENIVALCDVDWKYAKGVFDEFPNAKKYWDYRKMYDEMGKSIDGVIIATADHTHAIITADA 122 ++ LCDVD + A FP AK Y DYR++ D+ GK+ID V ++T DHTHA I A Sbjct: 72 TDVAFLCDVDDRRAANSLKNFPKAKYYKDYRELLDKEGKNIDAVTVSTPDHTHAQIAMAA 131 Query: 123 MTMGKHVYCQKPLTHSVYESRLLTKLAASTGVVTQMGNQGASGEGTDLVCEWIWNGEIGE 182 M +GKHVY QKPLTH +YE+R+LT+ A VVTQMGNQGASG+G + EW G IG+ Sbjct: 132 MQLGKHVYVQKPLTHDIYEARMLTEAANRYKVVTQMGNQGASGDGVRRLQEWYDAGRIGK 191 Query: 183 VTKVECATDRPIWPQGLNAPEKADRIPNTLNWDLFTGPAKLNPYNNVYHPWNWRGWWDYG 242 V V C T+RP+WPQG++ P IP L+WDL+ G A Y N P+NWRGWWDYG Sbjct: 192 VHTVYCWTNRPVWPQGISWPTGKAEIPKELDWDLWLGSAPYKEYVNKLVPFNWRGWWDYG 251 Query: 243 TGALGDMACHILHQPFRALKLGYPTKVEGS---------STLLLSACAPQAQHVKMIFPA 293 TGA+GDM CH++ PFR L L P VE S L P + HV + F Sbjct: 252 TGAIGDMGCHLVEPPFRVLGLDTPISVECSVGSVYVDEFKRAYLPESCPPSSHVILTFA- 310 Query: 294 RDNMPKVALPEVEVHWYDGGMMPERPKGFPEGKQLMGPGGGLTIFHGTKDTLICGCYGEQ 353 PK EV+VHW DGG+ PERP+ + G +F GTK +IC YG+ Sbjct: 311 --KTPKTK-HEVQVHWMDGGIKPERPEELGPNESF---GDNGVLFIGTKGKMICETYGKN 364 Query: 354 PFL--LSGRVPNAPKV-CRRVTCSHEMDWVRACKEDKS--NRVMPKADFSESGPMNEMVV 408 P L LS + K+ R+ E + + + + ++ + F +GP+ E ++ Sbjct: 365 PKLLPLSRNESDKTKITIPRIANQEEGHYTQFAEAAIAGYGKMELSSPFEIAGPLTETLL 424 Query: 409 MGVLAIR--------------LQGLNKTLEWDGANMCFTNIGD-NETLRTCIKDGFTI 451 + LAIR G + + WD M TN + N+ ++ + G+T+ Sbjct: 425 IANLAIRGTDVQRRDAAGKISYPGRDIKMLWDKVKMKVTNFDEVNQFVKREYRKGWTL 482 Lambda K H 0.319 0.136 0.444 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: 698 Number of extensions: 38 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 491 Length of database: 484 Length adjustment: 34 Effective length of query: 457 Effective length of database: 450 Effective search space: 205650 Effective search space used: 205650 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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 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