Align phosphoglucomutase (alpha-D-glucose-1,6-bisphosphate-dependent) (EC 5.4.2.2) (characterized)
to candidate 3608505 Dshi_1900 Phosphomannomutase (RefSeq)
Query= BRENDA::Q8PGN7 (450 letters) >FitnessBrowser__Dino:3608505 Length = 456 Score = 474 bits (1221), Expect = e-138 Identities = 245/450 (54%), Positives = 308/450 (68%), Gaps = 7/450 (1%) Query: 5 LPAFKAYDIRGRVPDELNEDLARRIGVALAAQLDQGPVVLGHDVRLASPALQEALSAGLR 64 L FKAYD+RGR+ D L+ ++A+ +G A+A L VV+G D+R +SPAL EAL AGLR Sbjct: 4 LACFKAYDVRGRIGDTLDTEIAQDVGRAVAEVLGARCVVVGRDIRDSSPALCEALGAGLR 63 Query: 65 ASGRDVIDIGLCGTEEVYFQTDYLKAAGGVMVTASHNPMDYNGMKLVREQARPISSDTGL 124 A+G DV DIGLCGTEEVYF TD+L A GVMVTASHNP+DYNG K+V ARP+ D Sbjct: 64 AAGADVRDIGLCGTEEVYFATDHLDACAGVMVTASHNPIDYNGFKIVGRGARPLP-DAQF 122 Query: 125 FAIRDTVAADT-AAPGEPTASEQSRTDKTAYLEHLLSYVDRSTLKPLKLVVNAGNGGAG- 182 AI A AAP + + + AY+ + S+VD + L P+ +V NAGNG AG Sbjct: 123 RAIERLAATRAFAAPTAQSGTHLEADTRAAYVARVCSFVDPAALGPVHVVANAGNGCAGS 182 Query: 183 ----LIVDLLAPHLPFEFVRVFHEPDGNFPNGIPNPLLPENRDATAKAVKDNGADFGIAW 238 +I L A E R+ H PD FPNGIPNPLLPEN+ AT+ A+ GAD GIAW Sbjct: 183 TFDAVIAALEAGGAKIEVTRLHHAPDARFPNGIPNPLLPENQPATSAAITRAGADLGIAW 242 Query: 239 DGDFDRCFFFDHTGRFIEGYYLVGLLAQAILAKQPGGKVVHDPRLTWNTVEQVEEAGGIP 298 DGDFDRCFFFD TG FI G ++VGLLA+AIL + PG +V+DPR+ WNT VE AGG Sbjct: 243 DGDFDRCFFFDETGAFIPGEFVVGLLAEAILEQTPGASIVYDPRVVWNTRRIVEAAGGAA 302 Query: 299 VLCKSGHAFIKEKMRSENAVYGGEMSAHHYFREFAYADSGMIPWLLIAELVSQSGRSLAD 358 VL K+GH +K+ MR +A YGGEMSAHHYFR+F + DSGMIPWLL+ E +S+SGR L+ Sbjct: 303 VLSKTGHVLVKDTMRRNDAAYGGEMSAHHYFRDFMFCDSGMIPWLLMLERLSKSGRPLSA 362 Query: 359 LVEARMQKFPCSGEINFKVADAKASVARVMEHYASLSPELDYTDGISADFGQWRFNLRSS 418 V ++ P SGEINF+V+DA +A + +HYA + +D DG+S +F WRFNLR+S Sbjct: 363 AVAEMRRRHPSSGEINFRVSDAARVMATLRQHYADSAEHIDTLDGVSMEFADWRFNLRAS 422 Query: 419 NTEPLLRLNVETRGDAALLETRTQEISNLL 448 NTEPLLRLNVET AALL+ R EI +++ Sbjct: 423 NTEPLLRLNVETLESAALLDRRVGEIRSMI 452 Lambda K H 0.319 0.136 0.404 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: 574 Number of extensions: 17 Number of successful extensions: 3 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: 450 Length of database: 456 Length adjustment: 33 Effective length of query: 417 Effective length of database: 423 Effective search space: 176391 Effective search space used: 176391 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: 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 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