Align D-lactate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized)
to candidate WP_088755700.1 CEJ45_RS13990 FAD-binding protein
Query= reanno::Cup4G11:RR42_RS17300 (497 letters) >NCBI__GCF_002213425.1:WP_088755700.1 Length = 495 Score = 736 bits (1899), Expect = 0.0 Identities = 368/497 (74%), Positives = 419/497 (84%), Gaps = 2/497 (0%) Query: 1 MNAPHEVSLVADDARRSALLAGLAKILPDAALLWKPEDTVPYECDGLAAYRQVPMAVALP 60 MNAP + S AR+ ++ L +++P +L+ EDT PYECDGLAAYRQ+PM V LP Sbjct: 1 MNAPAQPSFAP--ARQREVVDALRRVVPAHCVLFDEEDTRPYECDGLAAYRQLPMVVVLP 58 Query: 61 DNEDQVCAILRLCHSLQVPVVPRGAGTSLSGGAMPIATGLVLSLAKFKRIVSVDVRSRTA 120 +NE QV AI++ CH+LQV +VPRGAGT LSGGAMPIA G+V+S AKF +I+ +D SRTA Sbjct: 59 ENEAQVIAIMKACHALQVQIVPRGAGTGLSGGAMPIADGVVVSTAKFNQILKMDKYSRTA 118 Query: 121 VVQPGVRNLAISEAAAQYNLYYAPDPSSQIACTIGGNVSENSGGVHCLKYGLTVHNVLRV 180 VVQPGVRNLAISEAAA + LYYAPDPSSQIAC+IGGNV+ENSGGVHCLKYGLTVHNVLRV Sbjct: 119 VVQPGVRNLAISEAAAPHGLYYAPDPSSQIACSIGGNVAENSGGVHCLKYGLTVHNVLRV 178 Query: 181 RAVTMEGDVVEFGSEAPDAPGLDLLAAVIGSEGMLAVVTEVSVKLIPKPQLAQVIMASFD 240 R VT+EGDVVE GS A DAPGLDLLA IGSEGML VVTEV+VKL+PKPQ A+VIMASFD Sbjct: 179 RMVTIEGDVVELGSGALDAPGLDLLAVFIGSEGMLGVVTEVTVKLVPKPQAARVIMASFD 238 Query: 241 DVAKGGNAVADVIGAGIIPAGLEMMDKPATAAVEEFVRAGYDLDAAAILLCESDGTPEEV 300 DV KGGNAVA+VI AGIIPAGLEMMDK ++ VE FV+AGYD+DA AILLCESDGT EEV Sbjct: 239 DVVKGGNAVANVIAAGIIPAGLEMMDKTSSRMVEPFVKAGYDIDAEAILLCESDGTVEEV 298 Query: 301 AEEVERMSEVLRASGASRIQVSQSEPERLRFWSGRKNAFPAAGRISPDYYCMDGTIPRKH 360 EE+ RM++VL ASGA+ I SQSE ERLRFWSGRKNAFPAAGRISPDYYCMDGTIPRK Sbjct: 299 EEEIGRMTDVLNASGATAIACSQSEAERLRFWSGRKNAFPAAGRISPDYYCMDGTIPRKK 358 Query: 361 IGTLLKRIEEMERKYGLRCMNVFHAGDGNMHPLILFDGADQDEWHRAELFGSDILESCVE 420 + +L I EME+KYGLRC NVFHAGDGN+HPLILFD DE+HRAELFG++ILE CVE Sbjct: 359 LAQVLLGIAEMEKKYGLRCANVFHAGDGNLHPLILFDANIADEFHRAELFGAEILELCVE 418 Query: 421 LGGTVTGEHGVGVEKLNSMCVQFSAQERDLFFGVKAAFDPARLLNPDKAIPTLARCAEYG 480 +GGT+TGEHGVG+EK+NSMCVQFS ER+ FF +K AFDPA LLNPDKAIPTL RCAEYG Sbjct: 419 VGGTITGEHGVGIEKINSMCVQFSPAEREAFFKLKRAFDPAFLLNPDKAIPTLHRCAEYG 478 Query: 481 RMHVKRGLLPHPDLPRF 497 +MHV+RG L PDLPRF Sbjct: 479 KMHVQRGQLRFPDLPRF 495 Lambda K H 0.319 0.136 0.402 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: 757 Number of extensions: 19 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: 497 Length of database: 495 Length adjustment: 34 Effective length of query: 463 Effective length of database: 461 Effective search space: 213443 Effective search space used: 213443 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 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