Align Phosphoglucosamine/phosphogalactosamine mutase; PGlcNM; EC 5.4.2.10; EC 5.4.2.13 (characterized)
to candidate WP_009123552.1 HMPREF9446_RS00850 phosphoglucosamine mutase
Query= SwissProt::Q976E4 (455 letters) >NCBI__GCF_000195635.1:WP_009123552.1 Length = 462 Score = 217 bits (552), Expect = 7e-61 Identities = 147/466 (31%), Positives = 232/466 (49%), Gaps = 37/466 (7%) Query: 9 GVRGIVN----KELTPELVLKLSKAIGTFFGK-----NSKILVGRDVRAGGDMLVKIVEG 59 G+RG + + L P ++K + A T K ++KI+VGRD R G+M+ +V G Sbjct: 9 GIRGTIGGGAGEGLNPLDIVKFTSAYATLIRKTCTVKSNKIVVGRDARISGEMVKNVVVG 68 Query: 60 GLLSVGVEVYDGGMAPTPALQYAVKTLGYDGGVVITASHNPAPYNGIKVVDKDGIEIRRE 119 L+ +G +V D +A TP + AV G GG+++TASHNP +N +K++++ G + Sbjct: 69 TLMGMGWDVVDIDLASTPTTELAVTMEGASGGIILTASHNPKQWNALKLLNEKGEFLNAA 128 Query: 120 KENEIEDLFFTERFNTIEWS-------SLTTEVKREDRVISTYVNGILSHVDIEKIKKKN 172 + E+ + E F+ + LT K D V++ L VD+E IKK N Sbjct: 129 EGQEVLRIAAAEEFDFADVDHLGSYRKDLTYNQKHIDSVLA------LELVDVEAIKKAN 182 Query: 173 YKVLIDPANSVGALSTPLVARALGC----KIYTI-NGNLDPLFSARQPEPTFDSLKETAE 227 ++V ID NSVG + P + + LG K+Y GN PEP +L + Sbjct: 183 FRVAIDCVNSVGGIILPELFKQLGVQHVEKLYCEPTGNFQ-----HNPEPLEKNLGDIMN 237 Query: 228 VVKTLKVDLGVAHDGDADRAIFIDSEGRVQWGDRSGTLLSYWASVKNPKAIKKIVTAVSS 287 ++K K D+ D D DR I +G++ + + ++ + P V+ +SS Sbjct: 238 LMKGGKADVAFVVDPDVDRLAMICEDGKMYGEEYTLVTVADYVLKHTPG---NTVSNLSS 294 Query: 288 SSLVEEYLSKYNIQVDWTKVGSVDIAHKVADENALAGFEENGGFMYPPHQYVRDGAMSFA 347 + + + KY + + VG V++ K+ + A+ G E NGG +YP Y RD + A Sbjct: 295 TRALRDVTRKYGQEYSASAVGEVNVTTKMKEVGAVIGGEGNGGVIYPASHYGRDALVGIA 354 Query: 348 LMLELLANENVSSAELFDRLPKYYLVKTKVDLKPGLMVEEIYKKILEVYSTSSVKAITID 407 L L LA+E +EL P Y++ K +VDL P V+ I K+ E+Y + ID Sbjct: 355 LFLSHLAHEGKKVSELRASYPAYFMAKNRVDLTPDTDVDAILAKVKEIYKNEEIN--DID 412 Query: 408 GVKIIGKDFWFLVRKSGTEPIIRIMAEAKDENVANNLVNELKKIVE 453 GVKI D W +RKS TEPIIR+ +EA A + ++ K++E Sbjct: 413 GVKIDFPDKWVHLRKSNTEPIIRVYSEAGTPEAAEEIGQQIMKVIE 458 Lambda K H 0.316 0.136 0.384 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: 472 Number of extensions: 25 Number of successful extensions: 5 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: 455 Length of database: 462 Length adjustment: 33 Effective length of query: 422 Effective length of database: 429 Effective search space: 181038 Effective search space used: 181038 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 24 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:
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