Align Phosphoglucosamine/phosphogalactosamine mutase; PGlcNM; EC 5.4.2.10; EC 5.4.2.13 (characterized)
to candidate WP_101447241.1 BD749_RS18370 phosphoglucosamine mutase
Query= SwissProt::Q976E4 (455 letters) >NCBI__GCF_002846395.1:WP_101447241.1 Length = 463 Score = 227 bits (579), Expect = 5e-64 Identities = 151/469 (32%), Positives = 252/469 (53%), Gaps = 21/469 (4%) Query: 1 MGKLFGTDGVRGIVNKE----LTPELVLKLSKAIGTFFGK---NSKILVGRDVRAGGDML 53 M + G+RG + + LTP V+K + A GT+ + N+ I+VGRD R GDM+ Sbjct: 1 MALIKSISGIRGTIGGQAGEALTPVDVVKFAAAFGTWVLQTTGNNTIIVGRDARLSGDMV 60 Query: 54 VKIVEGGLLSVGVEVYDGGMAPTPALQYAVKTLGYDGGVVITASHNPAPYNGIKVVDKDG 113 K+V L +G+ V D G++ TP ++ AV GG+++TASHNP +N +K++++ G Sbjct: 61 NKLVCATLQGLGINVVDLGLSTTPTVEMAVPDYKAGGGIILTASHNPKQWNALKLLNQKG 120 Query: 114 IEIRREKENEIEDLFFTERFNTIEWSSLTTEVKREDRVISTYVNGILS--HVDIEKIKKK 171 I + + +L E F + + L + +R+D + +++ IL+ VD++ IK+K Sbjct: 121 EFISDAEGKLVLELADKEAFEFAQVNDL-GKYQRDDEALQKHIDAILALPLVDVQAIKEK 179 Query: 172 NYKVLIDPANSVGALSTPLVARALGC-KIYTINGNLDPLFSARQPEPTFDSLKETAEVVK 230 ++ V ID NS G ++ P++ ALG K+ + D F PEP ++L+E + V++ Sbjct: 180 DFSVAIDCVNSSGGIAIPMLLEALGVNKVEKLFCEPDGNF-PHNPEPLPENLREISRVIE 238 Query: 231 TLKVDLGVAHDGDADRAIFIDSEGRVQWGDRSGTLLSYWASVKNPKAIKKIVTAVSSSSL 290 K DLG+ D D DR I+ +G + + + +S + + V+ +SS+ Sbjct: 239 KGKFDLGIVVDPDVDRLALINEDGSMFGEEYTLVAVSDYVL---QNQMGNTVSNLSSTRA 295 Query: 291 VEEYLSKYNIQVDWTKVGSVDIAHKVADENALAGFEENGGFMYPPHQYVRDGAMSFALML 350 + + K VG V++ + + ENA+ G E NGG +YP Y RD + AL L Sbjct: 296 LRDVTEKAGGSYYAAAVGEVNVVNMMKAENAIIGGEGNGGIIYPELHYGRDALVGIALFL 355 Query: 351 ELLANENVSSAELFDRLPKYYLVKTKVDLKPGLMVEEIYKKILEVYSTSSVKAITIDGVK 410 LA +S L P YY+ K K++L P + V+++ ++ E Y+ + TIDGVK Sbjct: 356 THLAKSGMSMTRLRASYPNYYISKNKIELTPEVDVDQVLIQMQERYAKQPIN--TIDGVK 413 Query: 411 IIGKDFWFLVRKSGTEPIIRIMAEAKD----ENVANNLVNELKKIVEGK 455 I W +RKS TEPIIRI AE++ E++AN ++ ++K+I+ K Sbjct: 414 IEFDKEWVHLRKSNTEPIIRIYAESESNATAEHLANKIIADIKEIISTK 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: 485 Number of extensions: 23 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: 463 Length adjustment: 33 Effective length of query: 422 Effective length of database: 430 Effective search space: 181460 Effective search space used: 181460 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