Align D-lactate oxidase and glycolate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized)
to candidate WP_101289457.1 CXZ10_RS11675 FAD-binding oxidoreductase
Query= reanno::psRCH2:GFF3772 (499 letters) >NCBI__GCF_002844595.1:WP_101289457.1 Length = 475 Score = 162 bits (409), Expect = 3e-44 Identities = 145/478 (30%), Positives = 225/478 (47%), Gaps = 40/478 (8%) Query: 21 LLAELQAQLPDLDILHRSEDLKPYECDGLSAYRTTPLLVVLPERIEQVETLLKLCHQRGV 80 LL+ A + L D Y + YR LV+ P +V +L+L H+ Sbjct: 9 LLSRFAALVGPGHALVEEADKARYLVEWRDLYRGETPLVLRPANTAEVAAILRLAHETRT 68 Query: 81 PVVARGAGTGLSGGALPL--EQGILLVMARFNKILEVDPAGRFARVQPGVRNLAISQAAA 138 +V +G TGL GG +P+ + I++ + R +K+ +DP G V+ G+ ++ AA Sbjct: 69 AIVPQGGNTGLVGGQVPIPGQHEIVVSLERLDKVRSIDPLGNSMIVEAGMPLASVHAAAE 128 Query: 139 PYELYYAPDPSSQIACSIGGNVAENAGGVHCLKYGLTVHNLLKVDILTVEGERMTLGSDA 198 + + +S +C IGGN+A NAGG L YG + +L ++++ +G R+ G Sbjct: 129 AADRMFPLTLASLGSCQIGGNIATNAGGTAVLAYGNARNLVLGLEVVLADG-RIWNGLRQ 187 Query: 199 L--DSPGFDLLALFTGSEGMLGIVTEVTVKLLPKPQVAKVLLAAFDSVEKAGRAVGDI-- 254 L D+ G+DL LF GSEG LGI+T ++L +P + + AAF SV A+G Sbjct: 188 LGKDNAGYDLKQLFIGSEGTLGIITAAALRLRHRP---RGVAAAFVSVGSPAAALGLFAR 244 Query: 255 --IAAGIIPGGLEMMDNLSIRAAEDFIHAGYPVDAEA---ILL---CELDGVEADVHDDC 306 AAG G E+M L++ A I A A +L+ L G EAD Sbjct: 245 AQAAAGFGLTGFELMSGLAMEFALRHIPGARLPTAPAPWYVLIEVSSSLSGSEAD----- 299 Query: 307 ARVSEVLKLAGAT----EVRLAKDEAERVRFWAGRKNAFPAVGRISPDYYCMDGTIPRRE 362 A V ++L A A E +A+ + FW R + V + D ++P + Sbjct: 300 ATVLDILTGATAAGEALEAAVAQSFTQIDDFWRLR-HGMSEVQKHEGGSIKHDVSVPIGD 358 Query: 363 LPGVL-KGISDLSEQF-GLRVANVFHAGDGNMHPLILFDANQP------GELERAEDLGG 414 LP L + ++ + F G R H GDGN+H F+ +QP L R ++ Sbjct: 359 LPAFLEEAMAAVEAAFPGCRPVPFGHMGDGNIH----FNVSQPVGGDRQAFLARWNEMNA 414 Query: 415 KILELCVKVGGSITGEHGVGREKINQMCSQFNADELTLFHAVKAAFDPSGLLNPGKNI 472 + + K GS+ EHG+GR K++ + +L L +KAAFDP G+LNPG+ I Sbjct: 415 VVHGVVRKYDGSVAAEHGIGRLKVDLLAEVKPPLDLELMGRLKAAFDPLGILNPGRVI 472 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: 26 Number of successful extensions: 5 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: 475 Length adjustment: 34 Effective length of query: 465 Effective length of database: 441 Effective search space: 205065 Effective search space used: 205065 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