Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_073037960.1 BUB04_RS06135 phosphoglycerate dehydrogenase
Query= reanno::Cola:Echvi_2777 (630 letters) >NCBI__GCF_900129305.1:WP_073037960.1 Length = 527 Score = 197 bits (502), Expect = 7e-55 Identities = 125/360 (34%), Positives = 197/360 (54%), Gaps = 25/360 (6%) Query: 233 INVLLLENVHPIGVEIMKQ-EGYNVEVVSSAMSEEELCEKIKNVSIIGIRSKTQITKKVL 291 + VL+ + + G+E ++ + VEV +++++ EELC+ IK + IRS T++T++V+ Sbjct: 1 MKVLVSDALAESGIEKLRAIPDFEVEV-NTSLTHEELCQIIKEYDALVIRSATKVTREVI 59 Query: 292 ENANRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLHDK 351 ENA+RL + IG + +D+ ++GI V N P N + E I+ ++ L RN+ Sbjct: 60 ENADRLKVIARAGIGLDNVDISAATKRGIVVMNTPEGNVITTAEHTIAMLMALSRNIPQA 119 Query: 352 TLKMHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD------IVE 405 T M G W K EV K LGIIG G IG ++ A+ + MNV +D + Sbjct: 120 TQSMKAGKWEKKKFRGKEVFNKTLGIIGIGRIGRVVADRAKGLKMNVIAFDPYIGPETIN 179 Query: 406 RLALGNATKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVV 465 +L + T L+ELL D I++H E +N++NK+ KMK+G ++N +RG +V Sbjct: 180 KLGVEAVT----LEELLARADYITVHTPMTQETRNLINKDAFRKMKRGVFIINCARGGIV 235 Query: 466 DVPALRDALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENI 525 + L DA++ G +AGAA+DVF EP P + L+ I TPH+G ST EAQEN+ Sbjct: 236 NEQDLYDAIQEGIVAGAALDVFVEEP-----PKDHPLLALDKVIATPHLGASTDEAQENV 290 Query: 526 AQFVPGKIIEYINSGNTFNSVNFPNIQ-------LPFLKDAHRL-IHIHQNAPGVLAKIN 577 A V ++I+Y+ G N+VN P I P+L+ A +L + Q PG +I+ Sbjct: 291 ALAVADQVIDYLLHGTIRNAVNAPAIDGEVLATLWPYLQLAEKLGSLVQQITPGAPEEIS 350 Score = 28.5 bits (62), Expect = 8e-04 Identities = 22/88 (25%), Positives = 39/88 (44%), Gaps = 6/88 (6%) Query: 546 VNFPNIQLPFLKDAHRLIHIHQNAPGVLAKINQVLASYKINI----VGQYLKTNEKIGYV 601 V + +L + H ++ + + PG + I L + INI VGQ L+ + I ++ Sbjct: 440 VRINDFRLEAAMEGHLVLIYNIDTPGTIGAIGTCLGRHNINISMMDVGQVLERGQNIIFL 499 Query: 602 ITDIDKRYSNDVIDALKEIEGTIRFRIL 629 TD +V+ L +E +IL Sbjct: 500 RTDTP--VPENVVQELLSLENVNIVQIL 525 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: 738 Number of extensions: 33 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: 527 Length adjustment: 36 Effective length of query: 594 Effective length of database: 491 Effective search space: 291654 Effective search space used: 291654 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