Align glycolate oxidase subunit glcD (characterized)
to candidate BPHYT_RS32905 BPHYT_RS32905 FAD-linked oxidase
Query= CharProtDB::CH_024646 (499 letters) >lcl|FitnessBrowser__BFirm:BPHYT_RS32905 BPHYT_RS32905 FAD-linked oxidase Length = 463 Score = 157 bits (397), Expect = 8e-43 Identities = 134/434 (30%), Positives = 198/434 (45%), Gaps = 18/434 (4%) Query: 47 DGLSAYRTRPLLVVLPKQMEQVTAILAVCHRLRVPVVTRGAGTGLSGGALPLEKGVLLVM 106 D A R RP + +LP+ E V L V R VV +G TGL+GGA P V L + Sbjct: 35 DWSDAPRMRPRMTLLPRNPEDVARALRVLGEHRQAVVVQGGLTGLAGGATPQAGEVALSL 94 Query: 107 ARFKEILDINPVGRRARVQPGVRNLAISQAVAPHNLYYAPDPSSQIACSIGGNVAENAGG 166 AR I + +G VQ GV + V ++ D ++ C IGGN A NAGG Sbjct: 95 ARVNAIESFDRIGGTLTVQAGVPLEQLQTFVEAEGWFFPLDLGARGTCQIGGNAATNAGG 154 Query: 167 VHCLKYGLTVHNLLKIEVQTLDGEALTLGSDAL-DSPGFDLLALFTGSEGMLGVTTEVTV 225 +++G +L +EV DG L++ + ++ G DL LF GSEG LGV T + + Sbjct: 155 NRVIRFGTMRDLILGLEVALPDGTMLSMMNRVTKNTTGIDLKQLFIGSEGTLGVITRIVL 214 Query: 226 KLLPKPPVARVLLASFDSVEKAGLAVGDIIANGIIPGGLEMMDNLSIRAAEDFIHA---- 281 KL PKP L + S + A + + A E+M + AA D H Sbjct: 215 KLEPKPSAVNTALCAVASFDDATRLLKYLRARLANLSSFELMWQDFMSAAMDIAHLKAPF 274 Query: 282 --GYPVDAEAILLCELDGVESDVQEDCERVNDILLKAG-ATDVRLAQDEAERVRFWAGRK 338 YPV +L+ L + D + E + +L G DV +AQ + WA R+ Sbjct: 275 GDTYPV---YVLIETLGESDDDDRRALEHSLERMLDDGIVQDVIIAQSIEHAKQLWAYRE 331 Query: 339 NAFPAVGRISPDYYCMDGTIPRRALPGVLEGI-ARLSQQYDLRVANVF-HAGDGNMHPLI 396 + ++ P + D IP + G +E A L++++ + F H GDGN+H L+ Sbjct: 332 TVGELLSKLKP-HAAFDIGIPMDRMNGFVEDARAALNERFSQQAHLFFGHLGDGNLH-LL 389 Query: 397 LFDANEPGEFARAEELGGKILELCVEVGGSISGEHGIGREKINQMCAQFNSDEITTFHAV 456 + + + EEL I +V G IS EHGIG K + ++ E+ + Sbjct: 390 SGPYADAADLLKVEEL---IYAAVNDVQGCISAEHGIGVIKQPFLHYSRSAPELDLMGKL 446 Query: 457 KAAFDPDGLLNPGK 470 KA DP G+LN G+ Sbjct: 447 KALLDPAGILNVGR 460 Lambda K H 0.320 0.140 0.415 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: 525 Number of extensions: 26 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: 499 Length of database: 463 Length adjustment: 34 Effective length of query: 465 Effective length of database: 429 Effective search space: 199485 Effective search space used: 199485 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: 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 preprint 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