Align D-lactate oxidase, iron-sulfur subunit (EC 1.1.3.15) (characterized)
to candidate WP_036833873.1 N784_RS07760 (Fe-S)-binding protein
Query= reanno::Smeli:SMc00926 (443 letters) >NCBI__GCF_000775615.1:WP_036833873.1 Length = 439 Score = 203 bits (517), Expect = 8e-57 Identities = 137/422 (32%), Positives = 211/422 (50%), Gaps = 32/422 (7%) Query: 38 CVHCGFCTATCPTYVVLGDELDSPRGRIYLIKDMLENGRAADSETVTHIDRCLSCLSCLT 97 CV CG+C CPT+ + E SPRGRI L+K M+ G+A I++CL C++C T Sbjct: 19 CVQCGYCLPVCPTFETMERETHSPRGRINLVK-MVAEGKADIDVLEDPIEKCLGCMACTT 77 Query: 98 TCPSGVDYMHLVDHARAHIEKTYKRPFKDRLARSVIAATLPYPSRFRLAL---------- 147 CPS V Y +++ A+ +E+ ++ + + + + +PS+ + Sbjct: 78 VCPSNVQYGQILEGAKDVVEQNKQKSKPQKGVENFLFDSF-FPSKGWMDTLGNATWLYQK 136 Query: 148 -GAAGLARPLAGLLKRVPF-LRTLGVMLDLAPSALPAARGAKPAVYAAKGTPRARVALLT 205 G +AR L L K P + ++ PS P R + Y +K A++A T Sbjct: 137 SGVQKVARKL-NLTKIAPLNMEHFEKVIPDLPS--PKERKKRANRYISKRPATAKIAFFT 193 Query: 206 GCAQPVLRPEINDATIRLLTGQGVEVVVSAGEGCCGALVHHMGRDEQALQAGRHNIDVWL 265 GC + E N TI LL G EV++ + CCGAL H G+ +++++ + NI Sbjct: 194 GCVMDSMFFETNKNTIHLLVKSGAEVILPKQQTCCGALHAHSGKVDESIELAKANI---- 249 Query: 266 KAAEEDGLDAIIITASGCGTTIKDYGHMLRLDPAYAEKAARVSALAKDVTEYLATLDLPE 325 KA EE+ +D II A GCG + +Y H+ + E+A + KD+T+ L LD E Sbjct: 250 KAFEEEQVDYIINNAGGCGARLIEYHHLFEEGSEWHERAKKFVTKVKDITQILVELDQIE 309 Query: 326 QGAR-NLTVAYHSACSMQHGQKITSAPKQLL-KRAGFSVREPAEGHLCCGSAGTYNILQP 383 + TV Y +C M + Q + PKQLL K G +++E CCGSAGTYN+LQ Sbjct: 310 YTKPVHKTVTYQPSCHMTNVQGVIEPPKQLLNKIPGLTLKELKRPEFCCGSAGTYNMLQY 369 Query: 384 EISAKLKARKVRNIEATKPEVIATGNIGCITQIASGT-------EIPILHTVELLDWAYG 436 + S K+ K+ ++ +TK + T N GC+ Q+ G E+ +H V+LL A Sbjct: 370 DESMKILDMKMEDVCSTKASDVVTTNPGCLLQMKLGIEREGTTGEMEAVHIVDLL--AQA 427 Query: 437 GP 438 GP Sbjct: 428 GP 429 Score = 27.7 bits (60), Expect = 8e-04 Identities = 11/31 (35%), Positives = 16/31 (51%) Query: 32 ETILRKCVHCGFCTATCPTYVVLGDELDSPR 62 E + KC+ C CT CP+ V G L+ + Sbjct: 63 EDPIEKCLGCMACTTVCPSNVQYGQILEGAK 93 Lambda K H 0.320 0.135 0.409 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: 460 Number of extensions: 20 Number of successful extensions: 7 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 443 Length of database: 439 Length adjustment: 32 Effective length of query: 411 Effective length of database: 407 Effective search space: 167277 Effective search space used: 167277 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