Align phosphopentomutase (EC 5.4.2.7) (characterized)
to candidate Dsui_3057 Dsui_3057 phosphoglucosamine mutase
Query= BRENDA::Q6I7B6 (450 letters) >lcl|FitnessBrowser__PS:Dsui_3057 Dsui_3057 phosphoglucosamine mutase Length = 451 Score = 125 bits (315), Expect = 2e-33 Identities = 131/479 (27%), Positives = 206/479 (43%), Gaps = 65/479 (13%) Query: 2 RLFGTAGIRGTLWEK-VTPELAMKVGMAVGTYKSGK----------ALVGRDGRTSSVML 50 + FGT G+RG + E +TP+ AM++G + G + L+G+D R S ML Sbjct: 4 KYFGTDGVRGRVGEAPITPDFAMRLGYSAGQVLVAQDGLPAGERPAVLIGKDTRISGYML 63 Query: 51 KNAMISGLLSTGMEVLDADLIPTPALAWGTRKLA-DAGVMITASHNPPTDNGVKVFNGDG 109 + A+ +G + G++V +PTPA+A+ TR L AG++I+ASHNP DNG+K F+ G Sbjct: 64 EAALEAGFSAAGVDVCLVGPMPTPAVAYLTRALRLQAGIVISASHNPFYDNGIKFFSAQG 123 Query: 110 TEFYVEQERGLEE-------IIFSGNFRKARWDEIKPVRNVEVIPDYINAVLDFVGHETN 162 T+ E +E + S KAR + R +E LD G Sbjct: 124 TKLPDAVEHAIEAGVEAPMGCVPSDRLGKARRIDDARGRYIEFCKSTFPNDLDLRG---- 179 Query: 163 LKVLYDGANGAGSLVAPYLLREMGAKVLSVNAHVDG---HFPGRKPEPRYENIAYLGKLV 219 LK++ D A+GA +AP + E+GA V+++ DG + P+ A LG+ Sbjct: 180 LKIVVDCAHGAAYHIAPDVFHELGADVVAIGNRPDGLNINAAVGATAPKALKEAVLGQ-- 237 Query: 220 RELGVDLAIAQDGDADRIAVFDEKGNYVDEDTVIALFAKLYVEEHGGGTVVVSIDTGSRI 279 DL IA DGD DR+ + D +GN D D + L+A + + G V+ G+ + Sbjct: 238 ---RADLGIALDGDGDRLVMVDGEGNVYDGDQL--LYAIVRGRQALGPVAGVA---GTLM 289 Query: 280 DAVVERAGGRVVRIPLGQPHDGIKRYKAIFAAEPWKLVHPKFGP--WIDPFVT------- 330 + + + IP + G + W G +D T Sbjct: 290 TNLALEDALKALDIPFARAAVGDRYVLEKLVQNGWLYGGENSGHILCLDRHTTGDGIIAA 349 Query: 331 MGLLIKLIDENGPLSELVKEIPTYYLKKANVLCPDEY---KAEVVRRAAEEVERKLSSEI 387 + +L L + G L L+ ++ Y K NV P + + + A VE +L Sbjct: 350 LQVLAALRQQGGSLKALLGDLVLYPQKLINVPMPKGFPWQDSPAIAAAQRAVEAELDGRG 409 Query: 388 KEVLTISGFRIALNDGSWILIRPSGTEPKIRVVAEAPTEKRRDELFEMAYSTVSRIVKE 446 + +L+R SGTEP +RV+ E + L E V + V E Sbjct: 410 R-----------------VLLRASGTEPLLRVMVEGRDGELIARLAEKLAGAVRQAVGE 451 Lambda K H 0.318 0.138 0.402 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: 486 Number of extensions: 29 Number of successful extensions: 6 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: 450 Length of database: 451 Length adjustment: 33 Effective length of query: 417 Effective length of database: 418 Effective search space: 174306 Effective search space used: 174306 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: 51 (24.3 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