Align phosphomannomutase (EC 5.4.2.8) (characterized)
to candidate GFF3376 HP15_3318 phosphomannomutase
Query= BRENDA::P26276 (463 letters) >lcl|FitnessBrowser__Marino:GFF3376 HP15_3318 phosphomannomutase Length = 880 Score = 612 bits (1579), Expect = e-179 Identities = 299/455 (65%), Positives = 359/455 (78%) Query: 9 LPASIFRAYDIRGVVGDTLTAETAYWIGRAIGSESLARGEPCVAVGRDGRLSGPELVKQL 68 LP IFRAYDIRG+VG+TLTAE IGRAIGSE+ RG + +G DGR S P+L L Sbjct: 426 LPQDIFRAYDIRGIVGETLTAEGVEVIGRAIGSEARERGVDSLCIGYDGRHSSPDLADAL 485 Query: 69 IQGLVDCGCQVSDVGMVPTPVLYYAANVLEGKSGVMLTGSHNPPDYNGFKIVVAGETLAN 128 +G++ GC V VG VPTPVLY+A + L+ SGVM+TGSHNP +YNG KI++ GETL+ Sbjct: 486 ARGVMAAGCNVIHVGAVPTPVLYFATHELQTGSGVMVTGSHNPANYNGLKIMLGGETLSG 545 Query: 129 EQIQALRERIEKNDLASGVGSVEQVDILPRYFKQIRDDIAMAKPMKVVVDCGNGVAGVIA 188 E IQ L +RI+ D ASG GS D+ Y +I DIA+A P+KVVVD GNG+AG +A Sbjct: 546 EAIQKLYQRIQTGDFASGRGSQSTEDVRRAYLDRIVGDIAVAAPLKVVVDAGNGIAGELA 605 Query: 189 PQLIEALGCSVIPLYCEVDGNFPNHHPDPGKPENLKDLIAKVKAENADLGLAFDGDGDRV 248 P LIE LGC VIPLYCEVDG+FPNHHPDPGKP NL DLIA+V++E AD+GLAFDGDGDR+ Sbjct: 606 PMLIEELGCEVIPLYCEVDGDFPNHHPDPGKPANLADLIARVESEGADIGLAFDGDGDRL 665 Query: 249 GVVTNTGTIIYPDRLLMLFAKDVVSRNPGADIIFDVKCTRRLIALISGYGGRPVMWKTGH 308 GVVTN+G II+PDRL+MLFA+DVVSRNPGAD+++DVKC+RRL +IS GGRP+MWKTGH Sbjct: 666 GVVTNSGKIIWPDRLMMLFARDVVSRNPGADVLYDVKCSRRLAGVISEAGGRPIMWKTGH 725 Query: 309 SLIKKKMKETGALLAGEMSGHVFFKERWFGFDDGIYSAARLLEILSQDQRDSEHVFSAFP 368 SL+K KMKETGALLAGEMSGH+FF ERW+GFDDG+YSAARLLEIL + R S+ VF FP Sbjct: 726 SLMKAKMKETGALLAGEMSGHIFFGERWYGFDDGLYSAARLLEILGIEDRHSDEVFEDFP 785 Query: 369 SDISTPEINITVTEDSKFAIIEALQRDAQWGEGNITTLDGVRVDYPKGWGLVRASNTTPV 428 DISTPE+N+ VTE SKF II+ L +G+GNI+T+DG+RVDY GWGL RASNTTPV Sbjct: 786 DDISTPELNVQVTESSKFDIIKRLGESGDFGDGNISTIDGIRVDYADGWGLCRASNTTPV 845 Query: 429 LVLRFEADTEEELERIKTVFRNQLKAVDSSLPVPF 463 LVLRFEA+T+E LERIK+VFR+QL+ L F Sbjct: 846 LVLRFEAETDEALERIKSVFRDQLQKAAPDLVADF 880 Lambda K H 0.319 0.138 0.410 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: 1088 Number of extensions: 43 Number of successful extensions: 1 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: 463 Length of database: 880 Length adjustment: 38 Effective length of query: 425 Effective length of database: 842 Effective search space: 357850 Effective search space used: 357850 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 54 (25.4 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 paper from 2022 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