Align Phosphoglucosamine/phosphogalactosamine mutase; PGlcNM; EC 5.4.2.10; EC 5.4.2.13 (characterized)
to candidate WP_007691377.1 C447_RS04600 phosphoglucosamine mutase
Query= SwissProt::Q976E4 (455 letters) >NCBI__GCF_000336675.1:WP_007691377.1 Length = 454 Score = 266 bits (680), Expect = 1e-75 Identities = 167/457 (36%), Positives = 253/457 (55%), Gaps = 16/457 (3%) Query: 3 KLFGTDGVRGIVNKELTPELVLKLSKAIGTFFGKNSKILVGRDVRAGGDMLVKIVEGGLL 62 +LFG+ G+RG N+E+TPE L+++ A+GT G ++ +GRD RA G ML V GL+ Sbjct: 2 RLFGSSGIRGTANEEVTPEFSLRVAMAVGTVVG-GGRVALGRDTRASGPMLADAVASGLV 60 Query: 63 SVGVEVYDGGMAPTPALQYAVKTLGYDGGVVITASHNPAPYNGIKVVDKDGIEIRREKEN 122 SVG +V G PTPA+Q + G VVITASHNP NGIK+V DG+E E+ Sbjct: 61 SVGCDVDRLGALPTPAVQCYAEAEGVPA-VVITASHNPPTDNGIKLVGPDGVEFPIERLE 119 Query: 123 EIEDLFFTERFNTIEWSSLTTEVKREDRVISTYVNGILSHVDIEKIKKKNYKVLIDPANS 182 +ED+ E F+ W+ T + ++ + YV+ ++ V E+I + V +DP + Sbjct: 120 RVEDVLAAEEFDRAPWNE-TGDSRQVEGARRRYVDSVVDAVARERIAAADLTVALDPGHG 178 Query: 183 VGALSTPLVARALGCKIYTINGNLDPLFSARQPEPTFDSLKETAEVVKTLKVDLGVAHDG 242 GAL++P + R LGC++ T+N D F R PEP DSL + +V+ D+GVAHDG Sbjct: 179 AGALTSPGIFRELGCRVVTVNAQPDGSFPGRDPEPVPDSLGDLKRLVRATDADVGVAHDG 238 Query: 243 DADRAIFIDSEGRVQWGDRSGTLLSYWASVKNPKAIKKIVTAVSSSSLVEEYLSKYNIQV 302 DADRA+F+D G GD S L + A +P + V+AV+ S + + + + + Sbjct: 239 DADRAVFVDEHGAAITGDAS--LAALAAGALSPG--DRTVSAVTVSQRLVDVADRVDAGL 294 Query: 303 DWTKVGSVDIAHKVAD------ENALAGFEENGGFMYPPHQYVRDGAMSFALMLELLANE 356 + T VGS I ++ D +AG E NGG ++P ++ RDGA + A LEL+A E Sbjct: 295 ELTPVGSTRIVSRIRDLQHQGVSVPVAG-EGNGGVLFPEYRLARDGAYTAARFLELVA-E 352 Query: 357 NVSSAELFDRLPKYYLVKTKVDLKPGLMVEEIYKKILEVYSTSSVKAITIDGVKIIGKDF 416 +SA + D + Y+ +T V+ E + S + DG ++ D Sbjct: 353 RPASAVIAD-VGGYHNRRTAVEYDGDAERETLLDAAATYADASPGELDATDGYRLNFGDA 411 Query: 417 WFLVRKSGTEPIIRIMAEAKDENVANNLVNELKKIVE 453 W LVR+SGTEP IRI AEA++ + A +L ++++ +E Sbjct: 412 WVLVRESGTEPKIRIYAEARENDRAEHLATDVREALE 448 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: 468 Number of extensions: 22 Number of successful extensions: 7 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: 454 Length adjustment: 33 Effective length of query: 422 Effective length of database: 421 Effective search space: 177662 Effective search space used: 177662 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