Align Phosphonoacetaldehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_013094271.1 BC1002_RS32750 phosphonoacetaldehyde dehydrogenase
Query= SwissProt::Q92UV7 (485 letters) >NCBI__GCF_000092885.1:WP_013094271.1 Length = 482 Score = 604 bits (1557), Expect = e-177 Identities = 308/477 (64%), Positives = 375/477 (78%), Gaps = 4/477 (0%) Query: 9 AVRHEPMRIAGRLVDTDDRVEVRYPWNDTVVGTVPAGRAEHAREAFAIAAAYQPKLTRYE 68 A R E MRIAG+ TD+ +EV P+ + VVGTVPAGR EH ++AFA A A++P+LTR+E Sbjct: 8 AFRQESMRIAGQHTTTDELIEVFNPYTNEVVGTVPAGRPEHVQQAFAKAHAFKPRLTRFE 67 Query: 69 RQKILLATAEALAARKEEISDVITLELGISKADSLYEVGRAFDVFTLAGQMCIRDDGEIF 128 RQ+IL TAE L+ RKE+ + +IT E G+ D LYE RA+DV++ A Q+ I+DDGE++ Sbjct: 68 RQRILQRTAEMLSERKEDFARLITAESGLCWKDGLYEASRAYDVWSFAAQLTIKDDGEVY 127 Query: 129 SCDLTPHGKARKIFTMREPLTA-ISAITPFNHPLNMVAHKVAPAIATNNCVVVKPTELTP 187 SCD++P+GK RKIFT R PL ISAITPFNHPLNMV+HK+APAIATNN VV+KPTELTP Sbjct: 128 SCDISPNGKNRKIFTTRLPLLGVISAITPFNHPLNMVSHKLAPAIATNNRVVLKPTELTP 187 Query: 188 MTALLLADILYEAGLPPEMLSVVTGWPADIGMEMITNPHVDLVTFTGSVPVGKLIAANAH 247 +TAL LAD+LYEAGLPPEMLSVVTG P +G MIT+PH DLVTFTGSV VGK IA +A Sbjct: 188 LTALALADVLYEAGLPPEMLSVVTGNPRTMGDAMITDPHCDLVTFTGSVRVGKYIAQHAG 247 Query: 248 YKRQVLELGGNDPLIILNDLSDDDLARAADLAVAGATKNSGQRCTAVKRILCQESVADRF 307 Y+R VLELGGNDPLI++ D DL +AA LAV GATKNSGQRCTAVKRIL +SVAD F Sbjct: 248 YRRTVLELGGNDPLIVMEDA---DLDKAAQLAVTGATKNSGQRCTAVKRILVVQSVADAF 304 Query: 308 VPLVLERAKRLRFGDPMDRSTDLGTVIHEKAAALFEERVMRAAEEGADILYHPGRSGALL 367 V VL AK+L+ GDPMD S D+GTVI+E +A LFE RV A GA +L+ R GAL Sbjct: 305 VERVLVHAKKLKCGDPMDPSVDVGTVINEASAQLFERRVADAQAHGARVLHGAPRQGALF 364 Query: 368 PPIVVDRVPHQSDLVLEETFGPIIPIVRVPDDDDATITLSNSTAFGLSSGVCTNDYRRMQ 427 P VVD VP+ +LV EETFGP+IPI+RVPD + I +SNSTA+GLSSGVCTN + Sbjct: 365 HPTVVDHVPYDCELVREETFGPVIPIIRVPDAIEEVIRVSNSTAYGLSSGVCTNRLDYIT 424 Query: 428 KYIAGLKVGTVNIWEVPGYRIEMSPFGGIKDSGNGYKEGVIEAMKSFTNVKTFSLPW 484 +++ L+VGTVN+WEVPGYR EMSPFGGIKDSGNGYKEG++EAMKS++NV+T+S+PW Sbjct: 425 RFVRELEVGTVNVWEVPGYRTEMSPFGGIKDSGNGYKEGMVEAMKSYSNVRTWSMPW 481 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: 613 Number of extensions: 27 Number of successful extensions: 3 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: 482 Length adjustment: 34 Effective length of query: 451 Effective length of database: 448 Effective search space: 202048 Effective search space used: 202048 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