Align phosphomannose mutase (EC 5.4.2.8) (characterized)
to candidate WP_068330934.1 A3K86_RS10930 phosphoglucomutase/phosphomannomutase family protein
Query= metacyc::MONOMER-13382 (455 letters) >NCBI__GCF_001650345.1:WP_068330934.1 Length = 470 Score = 207 bits (526), Expect = 8e-58 Identities = 145/466 (31%), Positives = 221/466 (47%), Gaps = 21/466 (4%) Query: 5 FGTFGVRGIANEKITPEFAMKIGMAFGTLLKREGRKKPLVVVGRDTRVSGEMLKEALISG 64 FGT G R + E+ T + + A ++ E ++ V+G D R + Sbjct: 4 FGTGGWRALIGEEFTKDNVRLVAQALANIMLAENVQQNGFVIGYDRRFLSDKAAAWFAEV 63 Query: 65 LLSVGCDVIDVG-IAPTPAVQWATKHFNADGGAVITASHNPPEYNGIKLLEPNGMGLKKE 123 L G V + PTP V + +K A A ITASHNP +YNGIK+ G + Sbjct: 64 LAGNGIPVSFINKYVPTPIVMFKSKAIGATYSACITASHNPADYNGIKVFIEGGRDADEV 123 Query: 124 REAIVEELFFKEDFDRAKWYEIGEVRREDII------KPYIEAIKSKVDVEAIKKRKPFV 177 +E + K + + + + +I ++++I + +D++AIK+ V Sbjct: 124 ITGKIEHQIAQISAQDVKAVDFEQAQNDGVITVINPMNEFVDSIINFIDIDAIKRANLRV 183 Query: 178 VVDTSNGAGSLTLPYLLRELGCKVITVNAQPDGYFPARNPEPNEENLKEFMEIVKALGAD 237 V+D G L +L C V +N + F P PN L IV G D Sbjct: 184 VIDPMFGVAKNALQTVLISGRCDVDVINDGQNPAFGGLMPSPNAATLYRLKHIVAHEGYD 243 Query: 238 FGVAQDGDADRAVFIDENGRFIQGDKTFALVADAVLKEKGG-GLLVTTVATSNLLDDIAK 296 G+ DGDADR IDE G FI ++ L+ +L+ KG G +V +AT++LLD +A+ Sbjct: 244 IGIGTDGDADRLGIIDEKGNFIHPNEVLLLLYYYLLEYKGWKGSVVRNIATTHLLDKVAQ 303 Query: 297 KHGAKVMRTKVGDLIVARALYENNGTIGGEENGGVIFPEHVLGRDGAMTVAKVVEIFAKS 356 H K VG ++ + ++ +GGE +GG+ H+ G+DG + +VE+ + + Sbjct: 304 AHNEKCFEVPVGFKHISSQMEADDALLGGESSGGLTIRGHIKGKDGVFASSLLVEMISVT 363 Query: 357 GKKFSELIDEL-PKYYQIKTKR----HVEGDRHAIVNKV------AEMARERGYTVDTTD 405 GKK SE++DE+ KY T D+ + NK+ E A E V D Sbjct: 364 GKKLSEMLDEIYDKYGYAYTAEGDCTFKPADKERLYNKIYVERPLPEFA-EEVEKVSYAD 422 Query: 406 GAKIIFED-GWVLVRASGTEPIIRIFSEAKSKEKAQEYLNLGIELL 450 GAK+ F++ GW L R SGTEP++RIF E +SKEKA+ L E L Sbjct: 423 GAKVYFKNGGWALARFSGTEPLLRIFVEMESKEKAEAILEQMREFL 468 Lambda K H 0.317 0.138 0.391 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: 539 Number of extensions: 28 Number of successful extensions: 4 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: 470 Length adjustment: 33 Effective length of query: 422 Effective length of database: 437 Effective search space: 184414 Effective search space used: 184414 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