Align phosphomannose mutase (EC 5.4.2.8) (characterized)
to candidate 353476 BT3950 phosphoglucomutase/phosphomannomutase (NCBI ptt file)
Query= metacyc::MONOMER-13382 (455 letters) >lcl|FitnessBrowser__Btheta:353476 BT3950 phosphoglucomutase/phosphomannomutase (NCBI ptt file) Length = 462 Score = 254 bits (650), Expect = 3e-72 Identities = 166/443 (37%), Positives = 241/443 (54%), Gaps = 13/443 (2%) Query: 6 GTFGVRGIANEKITPEFAMKIGMAFGTLLKREGRKKP-LVVVGRDTRVSGEMLKEALISG 64 GT G G A E + P +K A+ TL+++ + + +VVGRD R+SGEM+K ++ Sbjct: 12 GTIG--GGAGEGLNPLDIVKFTSAYATLIRKTCKAQSNKIVVGRDARISGEMVKNVVVGT 69 Query: 65 LLSVGCDVIDVGIAPTPAVQWATKHFNADGGAVITASHNPPEYNGIKLLEPNGMGLKKER 124 L+ +G DV+D+ +A TP + A A GG ++TASHNP ++N +KLL +G L E Sbjct: 70 LMGMGWDVVDIDLASTPTTELAVTMEGACGGIILTASHNPKQWNALKLLNEHGEFLNAEE 129 Query: 125 EAIVEELFFKEDFDRAKWYEIGEVRRE-DIIKPYIEAIKS--KVDVEAIKKRKPFVVVDT 181 V + E+FD A +G R++ + +I+++ + VDVEAIKK V +D Sbjct: 130 GNEVLRIAEAEEFDYADVDHLGSYRKDLTYNQKHIDSVLALDLVDVEAIKKANFRVAIDC 189 Query: 182 SNGAGSLTLPYLLRELGCK-VITVNAQPDGYFPARNPEPNEENLKEFMEIVKALGADFGV 240 N G + LP LL LG K V + +P G F NPEP E+NL + M ++K AD Sbjct: 190 VNSVGGIILPELLERLGVKHVEKLYCEPTGNF-QHNPEPLEKNLGDIMNLMKGGKADVAF 248 Query: 241 AQDGDADRAVFIDENGRFIQGDKTFALVADAVLKEKGGGLLVTTVATSNLLDDIAKKHGA 300 D D DR I ENG + T VAD VLK G V+ ++++ L D+ +K+G Sbjct: 249 VVDPDVDRLAMICENGVMYGEEYTLVTVADYVLKHTPGN-TVSNLSSTRALRDVTRKYGM 307 Query: 301 KVMRTKVGDLIVARALYENNGTIGGEENGGVIFPEHVLGRDGAMTVAKVVEIFAKSGKKF 360 + + VG++ V + N IGGE NGGVI+P GRD + +A + A GKK Sbjct: 308 EYSASAVGEVNVVTKMKATNAVIGGEGNGGVIYPASHYGRDALVGIALFLSHLAHEGKKV 367 Query: 361 SELIDELPKYYQIKTKRHV--EGDRHAIVNKVAEMARERGYTVDTTDGAKIIFEDGWVLV 418 SEL P Y+ K + + E D AI+ KV E+ + ++ DG KI F D WV + Sbjct: 368 SELRATYPPYFIAKNRVDLIPEIDVDAILAKVKEIYKNE--EINDIDGVKIDFADKWVHL 425 Query: 419 RASGTEPIIRIFSEAKSKEKAQE 441 R S TEPIIR++SEA + A+E Sbjct: 426 RKSNTEPIIRVYSEASTMGAAEE 448 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: 494 Number of extensions: 31 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.
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