Align Phosphoglucosamine/phosphogalactosamine mutase; PGlcNM; EC 5.4.2.10; EC 5.4.2.13 (characterized)
to candidate WP_019387483.1 P735_RS0107910 phosphoglucosamine mutase
Query= SwissProt::Q976E4 (455 letters) >NCBI__GCF_000283015.1:WP_019387483.1 Length = 462 Score = 212 bits (540), Expect = 2e-59 Identities = 139/460 (30%), Positives = 238/460 (51%), Gaps = 26/460 (5%) Query: 10 VRGIVNKELTPELVLKLSKAIGTFFGK-----NSKILVGRDVRAGGDMLVKIVEGGLLSV 64 + G V + LTP +K + A G + + N K++VGRD R G M+ +V L+ + Sbjct: 14 IGGQVGENLTPIDAVKFASAYGVWLKQQRDKENYKVVVGRDARISGKMIQNLVMNTLIGL 73 Query: 65 GVEVYDGGMAPTPALQYAVKTLGYDGGVVITASHNPAPYNGIKVVDKDGIEIRREKENEI 124 G++V D G++ TP ++ AV DGG+++TASHNP +N +K++++ G + + +I Sbjct: 74 GIDVVDVGLSTTPTVEVAVPMEHADGGIILTASHNPKQWNALKLLNEKGEFLDAVEGAKI 133 Query: 125 EDLFFTERFNTIEWSSLTTEVKREDRVISTYVNGI--LSHVDIEKIKKKNYKVLIDPANS 182 D+ ++ + SL ++ + I ++ + L V+++ I++ +KV++D NS Sbjct: 134 LDIAESDNMIFADVDSL-GKITKNKAYIDLHIIEVLDLDLVNVKAIEEARFKVVVDGVNS 192 Query: 183 VGALSTPLVARALGCKIYTI----NGNLDPLFSARQPEPTFDSLKETAEVVKTLKVDLGV 238 G ++ PL+ LG + + NG+ PEP + L + ++ VK D G+ Sbjct: 193 TGGIAIPLLLERLGVDVVKLYCEPNGHF-----PHNPEPLKEHLTDLSDAVKKHNADFGI 247 Query: 239 AHDGDADRAIFIDSEGRVQWGDRSGTLLSYWASVKNPKAIKKIVTAVSSSSLVEEYLSKY 298 D D DR F+D G + + + + + + P V+ +SS+ + + K+ Sbjct: 248 VVDPDVDRLAFMDENGEMFGEEYTLVACADYVLSRTP---GNTVSNMSSTRALRDVTEKH 304 Query: 299 NIQVDWTKVGSVDIAHKVADENALAGFEENGGFMYPPHQYVRDGAMSFALMLELLANENV 358 + + VG V++ + + G E NGG +YP Y RD + AL L LLA++ + Sbjct: 305 GGTYEASAVGEVNVVKLMKKNKVVIGGEGNGGIIYPDAHYGRDALVGVALFLSLLADKKM 364 Query: 359 SSAELFDRLPKYYLVKTKVDLKPGLMVEEIYKKILEVYSTSSVKAITIDGVKIIGKDFWF 418 S + L P Y++ K K++L PGL V+ I K I + Y + TIDGVKI + W Sbjct: 365 SVSALRKTYPSYFMGKKKIELTPGLDVDGILKTIEKRYQIEQL--TTIDGVKIDFPESWV 422 Query: 419 LVRKSGTEPIIRIMAEAKDENVANNL----VNELKKIVEG 454 +RKS TEPIIRI EAK + A+ L + E+ +I +G Sbjct: 423 HLRKSNTEPIIRIYTEAKSQQEADVLGDKFIAEIGEIAKG 462 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: 502 Number of extensions: 34 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