Align Phosphonoacetaldehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_082798032.1 CAter10_RS02910 phosphonoacetaldehyde dehydrogenase
Query= SwissProt::Q92UV7 (485 letters) >NCBI__GCF_001584165.1:WP_082798032.1 Length = 487 Score = 575 bits (1481), Expect = e-168 Identities = 288/474 (60%), Positives = 362/474 (76%), Gaps = 5/474 (1%) Query: 12 HEPMRIAGRLVDTDDRVEVRYPWNDTVVGTVPAGRAEHAREAFAIAAAYQPKLTRYERQK 71 H+ MRIAG+LV + R+E+R+P+N+ ++G+VP + R AF IA A++ LTRYER + Sbjct: 17 HQNMRIAGKLVGNERRIEIRHPFNNALIGSVPKATVDDIRHAFQIARAFRSPLTRYERSR 76 Query: 72 ILLATAEALAARKEEISDVITLELGISKADSLYEVGRAFDVFTLAGQMCIRDDGEIFSCD 131 I+L TAE L A + ISD+IT E G+ K D+LYEVGRA DVF A + DDG++FSCD Sbjct: 77 IMLRTAELLRANADAISDLITAEAGLCKKDTLYEVGRACDVFVFAANQALVDDGQVFSCD 136 Query: 132 LTPHGKARKIFTMREPLT-AISAITPFNHPLNMVAHKVAPAIATNNCVVVKPTELTPMTA 190 LTPHGK RK++T++EPL AISAITPFNHPLN VAHKVAP+IATNN +V+KPTE TP++A Sbjct: 137 LTPHGKQRKVYTLKEPLLGAISAITPFNHPLNQVAHKVAPSIATNNRMVLKPTEKTPLSA 196 Query: 191 LLLADILYEAGLPPEMLSVVTGWPADIGMEMITNPHVDLVTFTGSVPVGKLIAANAHYKR 250 LLLADILYEAGLPPEM SVVTG PA+I EM+TNP VDLVTFTG VP+GK IAA A YKR Sbjct: 197 LLLADILYEAGLPPEMFSVVTGDPAEIADEMLTNPDVDLVTFTGGVPIGKYIAAKAVYKR 256 Query: 251 QVLELGGNDPLIILNDLSDDDLARAADLAVAGATKNSGQRCTAVKRILCQESVADRFVPL 310 Q+LELGGNDP+I++ D DL AA LAV+G+ KNSGQRCTA+KR++ ++VAD FV L Sbjct: 257 QILELGGNDPIIVMEDA---DLEEAATLAVSGSYKNSGQRCTAIKRMIVHQTVADEFVEL 313 Query: 311 VLERAKRLRFGDPMDRSTDLGTVIHEKAAALFEERVMRAAEEGADILYHPGRSGALLPPI 370 +L + K +++GDPMD D+GTVI ++A FE +V+ A + GA +LY R GAL P Sbjct: 314 LLNKTKAIKYGDPMDPHNDMGTVIDARSACAFEAKVIDAQQRGAKLLYGNLRDGALYSPT 373 Query: 371 VVDRVPHQSDLVLEETFGPIIPIVRVPDDDDATITLSNSTAFGLSSGVCTNDYRRMQKYI 430 V+D VP LV EETFGP+ P++R D DA I +SNST +GLSS VCTN + ++I Sbjct: 374 VLDHVPADCQLVAEETFGPVSPVIRCNDIADA-IRISNSTPYGLSSSVCTNRLDYITRFI 432 Query: 431 AGLKVGTVNIWEVPGYRIEMSPFGGIKDSGNGYKEGVIEAMKSFTNVKTFSLPW 484 L+VG+VN+ EVPGYR+E++PFGGIKDSG GYKEGV EAMKSF N KT+SLPW Sbjct: 433 RELQVGSVNVREVPGYRLELTPFGGIKDSGLGYKEGVQEAMKSFCNTKTYSLPW 486 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: 643 Number of extensions: 26 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: 487 Length adjustment: 34 Effective length of query: 451 Effective length of database: 453 Effective search space: 204303 Effective search space used: 204303 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