Align Phosphoglucosamine/phosphogalactosamine mutase; PGlcNM; EC 5.4.2.10; EC 5.4.2.13 (characterized)
to candidate WP_009135094.1 HMPREF9450_RS11515 phosphoglucosamine mutase
Query= SwissProt::Q976E4 (455 letters) >NCBI__GCF_000231275.1:WP_009135094.1 Length = 462 Score = 207 bits (528), Expect = 4e-58 Identities = 141/465 (30%), Positives = 237/465 (50%), Gaps = 34/465 (7%) Query: 9 GVRGIVN----KELTPELVLKLSKAIGTFF-----GKNSKILVGRDVRAGGDMLVKIVEG 59 G+RG + LTP ++K + A + G+ K+++GRD R G+M IVEG Sbjct: 9 GIRGTIGGAAGDNLTPLDLVKFTSAYAEWLKGEHPGRRLKVVIGRDARLSGEMAAAIVEG 68 Query: 60 GLLSVGVEVYDGGMAPTPALQYAVKTLGYDGGVVITASHNPAPYNGIKVVDKDGIEIRRE 119 L GV+V + G+A TP ++ AV DGG+++TASHNP +N +K+++ G + Sbjct: 69 TLCGCGVDVINIGLATTPTVELAVTGKQADGGIILTASHNPKQWNALKLLNSHGEFLNDA 128 Query: 120 KENEIEDLFFTERFNTIEWSSLTTEVKREDRVI------STYVNGILS--HVDIEKIKKK 171 + ++ L S E+ R RVI ++ G L+ D++ ++K Sbjct: 129 EGKKVLAL-------AQAGVSAYPEIDRIGRVIERSSYNDEHIRGALALKLADLDAVRKA 181 Query: 172 NYKVLIDPANSVGALSTPLVARALGCKIYTINGNLDPLFSARQPEPTFDSLKETAEVVKT 231 +KV++D NSVG + P + R +G ++ +N D F A PEP ++L E + V Sbjct: 182 KFKVVVDAVNSVGGVVIPKLLREMGVEVVELNCTPDGNF-AHNPEPIPENLTEISARVPA 240 Query: 232 LKVDLGVAHDGDADRAIFIDSEGRVQWGDRSGTLLSYWASVKNPKAIKKIVTAVSSSSLV 291 K DLG+ D D DR + +G + + + ++ + A V+ +SSS + Sbjct: 241 EKADLGIIVDPDVDRLALVCEDGTMFGEEYTLVAVADYVLTHTKGA---TVSNLSSSRAL 297 Query: 292 EEYLSKYNIQVDWTKVGSVDIAHKVADENALAGFEENGGFMYPPHQYVRDGAMSFALMLE 351 ++ K+ + VG V++ K+ + A+ G E NGG +YP Y RD + L L Sbjct: 298 KDVTEKHGCKYAAAAVGEVNVVTKMKEVAAVIGGEGNGGVIYPELHYGRDALVGVVLFLT 357 Query: 352 LLANENVSSAELFDRLPKYYLVKTKVDLKPGLMVEEIYKKILEVYSTSSVKAITIDGVKI 411 LLA + +++L P Y++ K K++L P + V+++ ++ Y+ V IDGVKI Sbjct: 358 LLAKSGLKASQLRATYPAYHISKNKIELTPDIDVDKVLAQMKAKYAGEQV--TDIDGVKI 415 Query: 412 IGKDFWFLVRKSGTEPIIRIMAEAKD----ENVANNLVNELKKIV 452 W +RKS TEPIIRI +E++D + +A ++ E++ IV Sbjct: 416 DFPAEWVHLRKSNTEPIIRIYSESRDKAAADALAEKIIGEIRAIV 460 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: 462 Number of extensions: 20 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