Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_012411500.1 NPUN_RS26385 phosphoglycerate dehydrogenase
Query= reanno::Cola:Echvi_2777 (630 letters) >NCBI__GCF_000020025.1:WP_012411500.1 Length = 526 Score = 170 bits (431), Expect = 1e-46 Identities = 111/346 (32%), Positives = 183/346 (52%), Gaps = 13/346 (3%) Query: 235 VLLLENVHPIGVEIMKQEGYNVEVVSSAMSEEELCEKIKNVSIIGIRSKTQITKKVLENA 294 VL+ +++ G++I+ Q V + +L E I + IRS T++T++++E Sbjct: 4 VLVSDSIDQAGIDILSQVA--TVDVKIGLKPAQLLEIIGEYDALMIRSSTRVTQEIIEAG 61 Query: 295 NRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLHDKTLK 354 +L +G +G + +D+ +GI V N+P NT + E A++ I+ L R++ D Sbjct: 62 TQLKIIGRAGVGVDNVDVPAATRRGIVVVNSPEGNTIAAAEHALAMILALSRHIPDANAS 121 Query: 355 MHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD--IVERLALGNA 412 + +G W++++ EV K LG++G G IG+ ++ +A+ MGM + YD I A Sbjct: 122 VKRGAWDRNSFVGAEVYKKTLGVVGLGKIGSHVAAVAKTMGMKLLAYDPFISTERAEQIG 181 Query: 413 TKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVVDVPALRD 472 ++ LD L + D I+LH+ E +++N + KMK A ++N +RG ++D AL Sbjct: 182 CQLVELDLLFQQADYITLHIPKTPETTHLINATTLAKMKPTARIINCARGGIIDEVALAA 241 Query: 473 ALESGHLAGAAVDVFPTEPKNNDEPFESELIGC-PNTILTPHIGGSTLEAQENIAQFVPG 531 AL++G + GAA+DVF +EP ESEL ILTPH+G ST EAQ N+A V Sbjct: 242 ALKAGKIGGAALDVFESEPLG-----ESELRSLGKEVILTPHLGASTAEAQVNVAIDVAE 296 Query: 532 KIIEYINSGNTFNSVNFPNI---QLPFLKDAHRLIHIHQNAPGVLA 574 +I + + ++VN P + L LK +L N G LA Sbjct: 297 QIRDVLLGLPARSAVNIPGLGPDVLEELKPYMQLAETLGNLVGQLA 342 Score = 31.2 bits (69), Expect = 1e-04 Identities = 15/67 (22%), Positives = 35/67 (52%), Gaps = 6/67 (8%) Query: 560 HRLIHIHQNAPGVLAKINQVLASYKINI----VGQYLKTNEKIGYVITDIDKRYSNDVID 615 + L +H++ PG++ K+ +L S+ +NI VG+ + + + + ID ++D Sbjct: 453 YMLFTLHRDMPGIIGKLGSLLGSFNVNIASMQVGRKIVRGDAV--MALSIDDPLPEGILD 510 Query: 616 ALKEIEG 622 + ++ G Sbjct: 511 EIIKVPG 517 Lambda K H 0.317 0.136 0.377 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: 644 Number of extensions: 35 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 630 Length of database: 526 Length adjustment: 36 Effective length of query: 594 Effective length of database: 490 Effective search space: 291060 Effective search space used: 291060 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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