Align Phosphonoacetaldehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_085635111.1 MGEO_RS02570 phosphonoacetaldehyde dehydrogenase
Query= SwissProt::Q92UV7 (485 letters) >NCBI__GCF_002115805.1:WP_085635111.1 Length = 479 Score = 694 bits (1790), Expect = 0.0 Identities = 341/476 (71%), Positives = 393/476 (82%) Query: 10 VRHEPMRIAGRLVDTDDRVEVRYPWNDTVVGTVPAGRAEHAREAFAIAAAYQPKLTRYER 69 +RHE MRI G VDTD R+EVRYP+ D V+GTVP G AEHAR AF IAA YQPKLTRYER Sbjct: 4 IRHEQMRIGGEKVDTDARLEVRYPYTDEVIGTVPMGTAEHARRAFEIAANYQPKLTRYER 63 Query: 70 QKILLATAEALAARKEEISDVITLELGISKADSLYEVGRAFDVFTLAGQMCIRDDGEIFS 129 +IL E + R++ ++ +TLELGI S+YE RA DV+ A ++DDGEIFS Sbjct: 64 SRILQRAGELIGERRDYLAKWLTLELGICHQHSIYETKRAQDVYQFAAAEALKDDGEIFS 123 Query: 130 CDLTPHGKARKIFTMREPLTAISAITPFNHPLNMVAHKVAPAIATNNCVVVKPTELTPMT 189 CDLT +GKARKIFTMREP+ AISAITPFNHPLNMV+HK+AP+IATNNC+V KPTELTP+T Sbjct: 124 CDLTHNGKARKIFTMREPVRAISAITPFNHPLNMVSHKIAPSIATNNCMVCKPTELTPLT 183 Query: 190 ALLLADILYEAGLPPEMLSVVTGWPADIGMEMITNPHVDLVTFTGSVPVGKLIAANAHYK 249 AL LADILYEAGLPPEM VVTG PADIG EM+TN ++D++TFTG VPVGKLIA+ A YK Sbjct: 184 ALTLADILYEAGLPPEMFQVVTGMPADIGDEMVTNENIDIITFTGGVPVGKLIASKAGYK 243 Query: 250 RQVLELGGNDPLIILNDLSDDDLARAADLAVAGATKNSGQRCTAVKRILCQESVADRFVP 309 R LELGGNDPLI+ NDLSD DL +AA +AVAGAT NSGQRCTA+KRIL QESVAD+FVP Sbjct: 244 RTALELGGNDPLIVCNDLSDADLDKAATIAVAGATGNSGQRCTAIKRILVQESVADKFVP 303 Query: 310 LVLERAKRLRFGDPMDRSTDLGTVIHEKAAALFEERVMRAAEEGADILYHPGRSGALLPP 369 LV+E+AK+++FGDP D +T+LG VIH +AA LFE+RV AA++GA +LY PGR GALLPP Sbjct: 304 LVVEKAKKIKFGDPQDPATELGCVIHAQAAELFEKRVYMAADQGAKVLYDPGRRGALLPP 363 Query: 370 IVVDRVPHQSDLVLEETFGPIIPIVRVPDDDDATITLSNSTAFGLSSGVCTNDYRRMQKY 429 IVVD VPH S+LV+EETFGPIIPIVRVPD+D+ + +SNST FGLSSGVCTND R Y Sbjct: 364 IVVDHVPHDSELVMEETFGPIIPIVRVPDNDEEVMRISNSTDFGLSSGVCTNDLNRAIAY 423 Query: 430 IAGLKVGTVNIWEVPGYRIEMSPFGGIKDSGNGYKEGVIEAMKSFTNVKTFSLPWP 485 I GL VGT NIWE PGYRIEMSPFGGIKDSGNG KEGVIEAMK FTNVKT+SLPWP Sbjct: 424 INGLNVGTCNIWEQPGYRIEMSPFGGIKDSGNGVKEGVIEAMKFFTNVKTYSLPWP 479 Lambda K H 0.320 0.136 0.399 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: 677 Number of extensions: 24 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: 485 Length of database: 479 Length adjustment: 34 Effective length of query: 451 Effective length of database: 445 Effective search space: 200695 Effective search space used: 200695 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