Align Phosphate propanoyltransferase; Phosphate acyltransferase PduL; Phosphotransacylase PduL; PTAC; Propanediol utilization protein PduL; EC 2.3.1.222 (characterized)
to candidate BWI76_RS23150 BWI76_RS23150 propanediol utilization phosphotransacylase
Query= SwissProt::Q9XDN5 (210 letters) >FitnessBrowser__Koxy:BWI76_RS23150 Length = 210 Score = 387 bits (995), Expect = e-113 Identities = 196/210 (93%), Positives = 203/210 (96%) Query: 1 MDKELLQSTVRKVLDEMRQRPIPLGVSNRHIHLSAQDYERLFPGHPISEKKALLQPGQYA 60 MDK+LL+STV KVLDEMR RPIPLGVSNRHIHLSA DYERLFPGHPISEKKALLQPGQYA Sbjct: 1 MDKQLLESTVSKVLDEMRLRPIPLGVSNRHIHLSAADYERLFPGHPISEKKALLQPGQYA 60 Query: 61 AEQTVTLVGPKGQLKNVRLLGPLRSVSQVEISRTDARTLGIAAPLRMSGNLKGTPGIRLV 120 AEQTVTLVGPKGQLKNVRLLGPLRSVSQVEISRTDARTLG+AAPLRMSGNLKGTPGIRLV Sbjct: 61 AEQTVTLVGPKGQLKNVRLLGPLRSVSQVEISRTDARTLGVAAPLRMSGNLKGTPGIRLV 120 Query: 121 SPFAELELPSGVIVAQRHIHMSPLDALILRVSHGDMVSVAIEGDDRGLIFNNVAIRVSPD 180 SPF ELEL SGVIVAQRHIHMSPLDALILRV+HGD VSVAIEGD+RGLIFNNVA+RVSPD Sbjct: 121 SPFGELELTSGVIVAQRHIHMSPLDALILRVAHGDRVSVAIEGDERGLIFNNVAVRVSPD 180 Query: 181 MRLEMHIDTDEANAAGADNPHAFARLVGPR 210 MRLEMHIDTDEANAAGAD+P AFARLVGPR Sbjct: 181 MRLEMHIDTDEANAAGADSPQAFARLVGPR 210 Lambda K H 0.319 0.136 0.388 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: 295 Number of extensions: 9 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: 210 Length of database: 210 Length adjustment: 21 Effective length of query: 189 Effective length of database: 189 Effective search space: 35721 Effective search space used: 35721 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 (21.7 bits) S2: 45 (21.9 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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