Align Phosphoglucosamine/phosphogalactosamine mutase; PGlcNM; EC 5.4.2.10; EC 5.4.2.13 (characterized)
to candidate WP_048080275.1 EJ01_RS02135 phosphoglucosamine mutase
Query= SwissProt::Q976E4 (455 letters) >NCBI__GCF_000745485.1:WP_048080275.1 Length = 451 Score = 261 bits (667), Expect = 3e-74 Identities = 158/457 (34%), Positives = 253/457 (55%), Gaps = 19/457 (4%) Query: 3 KLFGTDGVRGIVNKELTPELVLKLSKAIGTFFG-KNSKILVGRDVRAGGDMLVKIVEGGL 61 +LFGT G+RG + E+T L+ + A T+ G K K ++G D R M+ + G+ Sbjct: 7 RLFGTSGIRGKIGSEITLNLITDVGMAAATYVGGKGRKAVIGYDTRTSNKMVENAIIAGI 66 Query: 62 LSVGVEVYDGGMAPTPALQYAVKTLGYDGGVVITASHNPAPYNGIKVVDKDGIEIRREKE 121 L G +V GM PTP + YA L D G++ITASHNP+ YNGIK+ + G+ +++E Sbjct: 67 LQCGCDVIRLGMVPTPLVGYAAMKLNADIGIMITASHNPSQYNGIKLWNPKGMAYTQDQE 126 Query: 122 NEIEDLFFTERFNTIEWSSLTTEVKREDRVISTYVNGILSHVDIEKIKKKNYKVLIDPAN 181 IE + + F+ + W + ++K +IS Y++ +L++VDI K KV++D AN Sbjct: 127 RTIEKIVHEKTFSKVSWEHIG-DIKDNSSIISGYMDDLLNNVDI----KGGLKVVVDCAN 181 Query: 182 SVGALSTPLVARALGCKIYTINGNLDPLFSARQPEPTFDSLKETAEVVKTLKVDLGVAHD 241 G+ +P V R GC++ T+N D F R PEP+ +L E +VVK D+G+AHD Sbjct: 182 GAGSFVSPTVLRKAGCEVLTLNSQPDGFFPGRMPEPSEANLSELMKVVKATGADIGIAHD 241 Query: 242 GDADRAIFIDSEGRVQWGDRSGTLLSYWASVKNPKAIKKIVTAVSSSSLVEEYLSKYNIQ 301 GDADR + ID EG++ D+ L+S K KIVT V +S V++ + + + Sbjct: 242 GDADRMVAIDDEGKMADFDKLLALVS-------SKIGGKIVTTVDASFCVDKCMKESGGE 294 Query: 302 VDWTKVGSVDIAHKVADENALAGFEENGGFMYPPHQYVRDGAMSFALMLELLANENVSSA 361 V TKVG V +A + + NA G E +G +++P DG +S ++E++ S Sbjct: 295 VVRTKVGDVHVAEAIVECNAAFGGEPSGTWLHPDFCMCPDGILSALKVIEIVEKYGPLS- 353 Query: 362 ELFDRLPKYYLVKTKVD---LKPGLMVEEIYKKILEVYSTSSVKAITIDGVKIIGKD-FW 417 +L + +P Y V+ K++ ++ L++E++ K+ L Y IDGV+I KD W Sbjct: 354 KLLNEIPSYPTVRDKIECENIQKTLIMEKV-KEELPDYFEDVNDVNFIDGVRISMKDGSW 412 Query: 418 FLVRKSGTEPIIRIMAEAKDENVANNLVNELKKIVEG 454 L+R SGTE IRI E ++ +A ++ + ++ +EG Sbjct: 413 VLIRPSGTESYIRITLEGRNVEIAQSIRTKSREFIEG 449 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: 470 Number of extensions: 22 Number of successful extensions: 6 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: 451 Length adjustment: 33 Effective length of query: 422 Effective length of database: 418 Effective search space: 176396 Effective search space used: 176396 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