Align D-lactate oxidase and glycolate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized)
to candidate WP_008410271.1 DESHY_RS02840 FAD-binding protein
Query= reanno::psRCH2:GFF3772 (499 letters) >NCBI__GCF_000315365.1:WP_008410271.1 Length = 459 Score = 319 bits (817), Expect = 1e-91 Identities = 167/457 (36%), Positives = 267/457 (58%), Gaps = 3/457 (0%) Query: 16 VDKAALLAELQAQLPDLDILHRSEDLKPYECDGLSAYRTT-PLLVVLPERIEQVETLLKL 74 + KA + L + +++ E+L Y D + + P +VV P + V ++K+ Sbjct: 1 MSKAQAIEALVKAIGKENVITEHEELVCYSFDATADVPSQMPDVVVTPRGTDDVVQIMKV 60 Query: 75 CHQRGVPVVARGAGTGLSGGALPLEQGILLVMARFNKILEVDPAGRFARVQPGVRNLAIS 134 Q +PV RGAGT L G +PL+ GI+L + NKI+E+D A VQPGV ++ Sbjct: 61 ASQYKIPVYPRGAGTNLCGDTIPLKGGIVLRTQKMNKIIEIDADNLVAVVQPGVVINDLN 120 Query: 135 QAAAPYELYYAPDPSSQIACSIGGNVAENAGGVHCLKYGLTVHNLLKVDILTVEGERMTL 194 A AP+ L Y PDP + ++GG+V+E +GG+ LKYG+T H ++ ++++ V+G Sbjct: 121 TAVAPFGLIYPPDPGTVATATMGGSVSECSGGLRGLKYGVTKHYVMGLEVVMVDGTVARF 180 Query: 195 GSDALDS-PGFDLLALFTGSEGMLGIVTEVTVKLLPKPQVAKVLLAAFDSVEKAGRAVGD 253 G + + +D++ LFTG+EG LGI+TE+TVKL+P P+ K +LA F +E AG V + Sbjct: 181 GGKTVKNVTAYDMVKLFTGAEGTLGIITEITVKLIPAPEAKKSMLAVFSKLEDAGNTVTE 240 Query: 254 IIAAGIIPGGLEMMDNLSIRAAEDFIHAGYPVDAEAILLCELDGVEADVHDDCARVSEVL 313 I+ + +IP +E+MD ++IR E+F G P DAEA+LL E+DG+ V + A V +V+ Sbjct: 241 IVRSKVIPATMEIMDQVTIRTVENFAKVGLPTDAEAVLLIEVDGIPEVVEREAATVVKVV 300 Query: 314 KLAGATEVRLAKDEAERVRFWAGRKNAFPAVGRISPDYYCMDGTIPRRELPGVLKGISDL 373 + +++AKD+ ER WA R+ A PA+ ++ P D T+PR L +L + ++ Sbjct: 301 EKNNGN-IKVAKDDKERDGLWAARRAALPALAQMKPTTVLEDATVPRSRLTEMLVALQNI 359 Query: 374 SEQFGLRVANVFHAGDGNMHPLILFDANQPGELERAEDLGGKILELCVKVGGSITGEHGV 433 ++++ L + HAGDGN+HP IL D E++R +I + +++GG+I+GEHG+ Sbjct: 360 AKKYNLMIGTFGHAGDGNLHPTILTDERNTEEMKRVHQAVDEIFKTALELGGTISGEHGI 419 Query: 434 GREKINQMCSQFNADELTLFHAVKAAFDPSGLLNPGK 470 G K + +F + + VK A DP LLNPGK Sbjct: 420 GMAKAKYLPLEFGEQGVEIMRKVKRALDPDNLLNPGK 456 Lambda K H 0.320 0.140 0.412 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: 561 Number of extensions: 22 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: 499 Length of database: 459 Length adjustment: 34 Effective length of query: 465 Effective length of database: 425 Effective search space: 197625 Effective search space used: 197625 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 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