Align D-lactate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized)
to candidate WP_004109665.1 RHSP_RS04425 FAD-binding protein
Query= reanno::Smeli:SMc00832 (479 letters) >NCBI__GCF_000359745.1:WP_004109665.1 Length = 479 Score = 789 bits (2037), Expect = 0.0 Identities = 392/479 (81%), Positives = 431/479 (89%) Query: 1 MPETIGFLKPRQAVLDRRREIVADLADLLPEGGLISDERGLKPFETDAFIAYRRMPLAVV 60 M E I F++PR VL RR IVADL+DLL LI + R L PFETDAF++YRR+PLAV Sbjct: 1 MAEAISFMEPRADVLARRSTIVADLSDLLAPECLIHEARELVPFETDAFVSYRRVPLAVA 60 Query: 61 LPETTEHVAAVLKYCSRYGIPIVPRGAGTSLSGGAIPQEDAIVVGLSKMSRTLDIDLFNR 120 LP TT VAAV+KYC RYGIPIVPRGAGTSLSGGAIPQEDA+V+GLSKM+R LDID NR Sbjct: 61 LPRTTAEVAAVMKYCHRYGIPIVPRGAGTSLSGGAIPQEDAVVLGLSKMNRILDIDYANR 120 Query: 121 TATVQAGVTNLNISDAVSADGFFYAPDPSSQLACTIGGNIGMNSGGAHCLKYGVTTNNLL 180 TATVQAGVTNLN+S++VSADGFFYAPDPSSQLACTIGGNIGMNSGGAHCLKYGVTTNNLL Sbjct: 121 TATVQAGVTNLNVSESVSADGFFYAPDPSSQLACTIGGNIGMNSGGAHCLKYGVTTNNLL 180 Query: 181 GVKMVLFDGTVIELGGKALDAPGYDLLGLVCGSEGQLGIVTEATVRLIAKPEGARPVLFG 240 GVK+VL DGT+I+LGGKALD+ GYDLLGLVCGSEGQLGIVTEATVRLIAKPEGARPVLFG Sbjct: 181 GVKLVLTDGTIIDLGGKALDSAGYDLLGLVCGSEGQLGIVTEATVRLIAKPEGARPVLFG 240 Query: 241 FASSESAGSCVADIIGSGIIPVAIEFMDRPAIEICEAFAQAGYPLDVEALLIVEVEGSEA 300 F +SE AG+CVAD+I +GIIPVAIEFMD+PAIEICEAFA+AGYPLDV ALLIVEVEGSEA Sbjct: 241 FDTSEEAGACVADVIAAGIIPVAIEFMDKPAIEICEAFAKAGYPLDVGALLIVEVEGSEA 300 Query: 301 EMDATLAGIIEIARRHGVMTIRESQSALEAALIWKGRKSAFGATGRIADYICMDGTVPLS 360 EMD LA I+EIAR H V T+RE QSA EAALIWKGRKSAFGATGRIADYICMDGTVPLS Sbjct: 301 EMDDMLASIVEIARSHSVKTVRECQSATEAALIWKGRKSAFGATGRIADYICMDGTVPLS 360 Query: 361 QLSHVLRRTGEIVAGYGLRVANVFHAGDGNMHPLILYNINDPEEAARAEAAGNDILKLCV 420 QLS+VL++T EIV GYGLRVANVFHAGDGNMHPLIL+N NDPE+AA+AEAAGNDIL+LCV Sbjct: 361 QLSYVLKKTAEIVHGYGLRVANVFHAGDGNMHPLILFNANDPEDAAKAEAAGNDILRLCV 420 Query: 421 EAGGCLTGEHGVGIEKRDLMLHQYSRADLGQQMAARAAFDPQWLMNPSKVFPLEGRPAA 479 +AGGCLTGEHGVGIEKRDLM HQY++ DL Q MA RAAFDP W++NPSKVFPL+GR AA Sbjct: 421 DAGGCLTGEHGVGIEKRDLMRHQYAKVDLDQMMAVRAAFDPGWILNPSKVFPLDGRDAA 479 Lambda K H 0.320 0.138 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: 860 Number of extensions: 28 Number of successful extensions: 1 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: 479 Length of database: 479 Length adjustment: 34 Effective length of query: 445 Effective length of database: 445 Effective search space: 198025 Effective search space used: 198025 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