Align Phosphonoacetaldehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_013091457.1 BC1002_RS18170 phosphonoacetaldehyde dehydrogenase
Query= SwissProt::Q92UV7 (485 letters) >NCBI__GCF_000092885.1:WP_013091457.1 Length = 483 Score = 518 bits (1334), Expect = e-151 Identities = 279/477 (58%), Positives = 332/477 (69%), Gaps = 5/477 (1%) Query: 9 AVRHEPMRIAGRLVDTDDRVEVRYPWNDTVVGTVPAGRAEHAREAFAIAAAYQPKLTRYE 68 A R E +R+ G D ++V P+ VGTVP + R AF A AY+P L+RYE Sbjct: 10 AFRVEALRLGGERATRDRTLDVFDPYTGMRVGTVPLASMDDVRAAFDYALAYRPTLSRYE 69 Query: 69 RQKILLATAEALAARKEEISDVITLELGISKADSLYEVGRAFDVFTLAGQMCIRDDGEIF 128 R +IL A L R E+ SD+I+LE G+SK DS YE+GR DVF A +RDDG+ F Sbjct: 70 RSQILERAAVLLRERIEQASDLISLESGLSKQDSRYEIGRVADVFRFASFEALRDDGQSF 129 Query: 129 SCDLTPHGKARKIFTMREPLTA-ISAITPFNHPLNMVAHKVAPAIATNNCVVVKPTELTP 187 SCDLTPHGK R++F+ REPL I AITPFNHP+N VAHKVAPAIATNN VVVKP+E P Sbjct: 130 SCDLTPHGKKRRVFSQREPLAGVIVAITPFNHPMNQVAHKVAPAIATNNRVVVKPSEKVP 189 Query: 188 MTALLLADILYEAGLPPEMLSVVTGWPADIGMEMITNPHVDLVTFTGSVPVGKLIAANAH 247 ++AL LAD+LYEAGLP ML V+TG P +I E+IT+ V+LVTFTG V +GK IA A Sbjct: 190 LSALYLADLLYEAGLPAPMLQVMTGDPREIADELITHASVELVTFTGGVAIGKYIATKAG 249 Query: 248 YKRQVLELGGNDPLIILNDLSDDDLARAADLAVAGATKNSGQRCTAVKRILCQESVADRF 307 Y+R VLELGGNDPLI+L+D DL RAA LAV G+ KNSGQRCTAVKR+L Q+ VA F Sbjct: 250 YRRVVLELGGNDPLIVLDDA---DLERAATLAVQGSYKNSGQRCTAVKRMLVQQRVAAEF 306 Query: 308 VPLVLERAKRLRFGDPMDRSTDLGTVIHEKAAALFEERVMRAAEEGADILYHPGRSGALL 367 V+E+ + FGDP D S +GTVI AA LFE RV A GA + RSGAL Sbjct: 307 TERVVEKTRAWTFGDPFDASNQMGTVIDAAAAQLFEARVNEAVAAGARLRIGNERSGALY 366 Query: 368 PPIVVDRVPHQSDLVLEETFGPIIPIVRVPDDDDATITLSNSTAFGLSSGVCTNDYRRMQ 427 P V+D V LV EETFGP+ PI+ DDA I +SN T FGLSSGVCTN + Sbjct: 367 APTVLDNVDPSMTLVREETFGPVSPIIAFDTLDDA-IRISNGTPFGLSSGVCTNRQDAIT 425 Query: 428 KYIAGLKVGTVNIWEVPGYRIEMSPFGGIKDSGNGYKEGVIEAMKSFTNVKTFSLPW 484 ++I L+VGTVN+WEVPGYRIE++PFGGIKDSG GYKEGV EAMKSFTN+KTFSLPW Sbjct: 426 RFINELRVGTVNVWEVPGYRIELTPFGGIKDSGLGYKEGVQEAMKSFTNLKTFSLPW 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: 629 Number of extensions: 32 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: 483 Length adjustment: 34 Effective length of query: 451 Effective length of database: 449 Effective search space: 202499 Effective search space used: 202499 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 Apr 09 2024. 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