Align Phosphonoacetaldehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_047215084.1 PATSB16_RS16135 phosphonoacetaldehyde dehydrogenase
Query= SwissProt::Q92UV7 (485 letters) >NCBI__GCF_001931675.1:WP_047215084.1 Length = 484 Score = 525 bits (1353), Expect = e-153 Identities = 272/475 (57%), Positives = 340/475 (71%), Gaps = 5/475 (1%) Query: 11 RHEPMRIAGRLVDTDDRVEVRYPWNDTVVGTVPAGRAEHAREAFAIAAAYQPKLTRYERQ 70 R E +RI G V + ++V P+ + +VGTVP + R A+ IA Y+ +LTR+ER Sbjct: 12 RAEALRIGGEKVLRERVIDVFNPYTNELVGTVPKATQDDVRRAYGIARQYRSRLTRFERA 71 Query: 71 KILLATAEALAARKEEISDVITLELGISKADSLYEVGRAFDVFTLAGQMCIRDDGEIFSC 130 IL A L R E + +ITLE G+ K D++YE+GR DV A +RDDG+ FSC Sbjct: 72 NILNRAAALLRERTSEAAGLITLESGLCKKDAVYEIGRVADVLNFAATEALRDDGQAFSC 131 Query: 131 DLTPHGKARKIFTMREPLT-AISAITPFNHPLNMVAHKVAPAIATNNCVVVKPTELTPMT 189 DLTPHGK R++ T R+PL AI AITPFNHP+N VAHKVAP+IATNN +V+KP+E P++ Sbjct: 132 DLTPHGKKRRVITQRDPLLGAICAITPFNHPMNQVAHKVAPSIATNNRMVLKPSEKVPLS 191 Query: 190 ALLLADILYEAGLPPEMLSVVTGWPADIGMEMITNPHVDLVTFTGSVPVGKLIAANAHYK 249 A LAD+LYEAGLPPEML VVTG P +I E++TN +VDL+TFTG V +GK IAA A Y+ Sbjct: 192 AFYLADVLYEAGLPPEMLQVVTGDPREIADELLTNENVDLITFTGGVQIGKYIAAKAGYR 251 Query: 250 RQVLELGGNDPLIILNDLSDDDLARAADLAVAGATKNSGQRCTAVKRILCQESVADRFVP 309 R VLELGGNDPLI++ D DL +A+DLAV G+ KNSGQRCTAVKR+L Q VA RF Sbjct: 252 RIVLELGGNDPLIVMEDA---DLDKASDLAVQGSYKNSGQRCTAVKRMLVQRDVAARFTE 308 Query: 310 LVLERAKRLRFGDPMDRSTDLGTVIHEKAAALFEERVMRAAEEGADILYHPGRSGALLPP 369 LV+E+ + ++GDP D D+GTVI E+AA LFE RV A +GA +L R GAL PP Sbjct: 309 LVVEKTRAWKYGDPNDGGVDMGTVIDEEAARLFESRVNEAVAQGARLLAGNRRDGALYPP 368 Query: 370 IVVDRVPHQSDLVLEETFGPIIPIVRVPDDDDATITLSNSTAFGLSSGVCTNDYRRMQKY 429 V+DRV +V EETFGP+ PI+ D +A I +SN TAFGLSSGVCTN + ++ Sbjct: 369 TVIDRVDPAMTVVREETFGPVSPIITFGDIAEA-IHISNGTAFGLSSGVCTNRLDYITRF 427 Query: 430 IAGLKVGTVNIWEVPGYRIEMSPFGGIKDSGNGYKEGVIEAMKSFTNVKTFSLPW 484 + L+VGTVN+WEVPGYRIE++PFGGIKDSG GYKEGV EAMKSFTN KTF+LPW Sbjct: 428 ASELEVGTVNVWEVPGYRIELTPFGGIKDSGLGYKEGVQEAMKSFTNQKTFTLPW 482 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: 631 Number of extensions: 24 Number of successful extensions: 4 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: 484 Length adjustment: 34 Effective length of query: 451 Effective length of database: 450 Effective search space: 202950 Effective search space used: 202950 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