Align 3-hydroxypropionate dehydrogenase (EC 1.1.1.59) (characterized)
to candidate WP_047215454.1 PATSB16_RS18245 FAD-binding protein
Query= metacyc::MONOMER-15202 (579 letters) >NCBI__GCF_001931675.1:WP_047215454.1 Length = 530 Score = 350 bits (899), Expect = e-101 Identities = 222/540 (41%), Positives = 290/540 (53%), Gaps = 23/540 (4%) Query: 36 FDYIVVGAGTAGCLLANRLS-ADPANRVLLIEAGGRDNYHW-IHIPVGYLYCIN-NPRTD 92 +DY+VVGAG+ GC LA RL+ A P + L+EAG D++HW + P+G + + Sbjct: 3 YDYLVVGAGSGGCALAARLADALPERTIALLEAGP-DDHHWLVKTPLGLAGLVPFKSARN 61 Query: 93 WRFRTEPDPGLNGRSLIYPRGKTLGGCSSINGMLYLRGQARDYDGWAELTGDDAWRWDNC 152 W F T P P L+GR PRG+ LGG SSIN M+Y RG DYD WA+ G WRW + Sbjct: 62 WAFHTTPQPALDGRRGYQPRGRGLGGSSSINAMIYTRGHPLDYDAWAD-AGCPGWRWQDV 120 Query: 153 LPDFMRHEDHYRLDEGGDADPDHYKFHGHGGEWRIEKQRLKWQVLADFATAAVEAGVPRT 212 LP F R E + R G DA +HG G + R F A +AG Sbjct: 121 LPYFKRAEHNER---GADA------WHGTQGPLNVADLRSPNPFSMRFVEAGRQAGFAVN 171 Query: 213 RDFNRGDNEGVDAFEVNQRSGWRWNASKAFLRGVEQRGNLTVWHSTQVLKLDFASGEGSE 272 DFN EGV ++V Q++G RWNA++A+L G R NL V T L++ F EG Sbjct: 172 GDFNGASQEGVGLYQVTQKNGERWNAARAYLHG-RTRQNLHVMTGTSALRIVF---EGR- 226 Query: 273 PRCCGVTVERAGKKVVTTARCEVVLSAGAIGSPQLLQLSGIGPTALLAEHAIPVVADLPG 332 R GV V+R G++ AR E+VL+AGA SPQLL SGIGPT L IP + + PG Sbjct: 227 -RAVGVEVQRGGRRETLRARAEIVLAAGAFNSPQLLMCSGIGPTEHLQSLGIPALVEAPG 285 Query: 333 VGENLQDHLQIRSIYKVKGAKTLNTMANSLIGKAKIGLEYILKRSGPMSMAPSQLCIFTR 392 VG NLQDHL + V + + + + Y+ +R G S ++ F Sbjct: 286 VGANLQDHLDVIINKCVPSSDLIGFSPAGIAHLSGALFGYLRERRGVFSSNVAEAGGFLS 345 Query: 393 SSKEYEHPNLEYHVQPLSLEAFGQPLHDFPAITASVCNLNPTSRGTVRIKSGNPRQAPAI 452 S + P+L+ H + + LH + VC L P SRG V + S + RQAP I Sbjct: 346 SQPGLDRPDLQLHFLVGISDDHNRKLHVRHGFSCHVCVLRPKSRGNVTLASADARQAPVI 405 Query: 453 SPNYLSTEEDRQVAADSLRVTRHIASQPAFAKYDPEEFKPGVQYQSDEDLARLAGDIGTT 512 P +LS ED + LR+ R I + PA A++ +E QSD+ L L T Sbjct: 406 DPRFLSEPEDLEGLLRGLRIVRKILAAPALAEFGGKELY-SQDVQSDDGLRALIRARADT 464 Query: 513 IFHPVGTAKMGRDDDPMAVVDSHLRVRGVTGLRVVDASIMPTITSGNTNSPTLMIAEKAA 572 I+HPVGT +MG D AVVD LRVRG+ LRVVDASIMPT+ GNTN+PT+MIAEKAA Sbjct: 465 IYHPVGTCRMG--SDAAAVVDPQLRVRGIERLRVVDASIMPTLIGGNTNAPTIMIAEKAA 522 Lambda K H 0.318 0.135 0.418 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: 884 Number of extensions: 44 Number of successful extensions: 9 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: 579 Length of database: 530 Length adjustment: 36 Effective length of query: 543 Effective length of database: 494 Effective search space: 268242 Effective search space used: 268242 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 53 (25.0 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