Align phosphomannose mutase (EC 5.4.2.8) (characterized)
to candidate HSERO_RS06955 HSERO_RS06955 phosphoglucosamine mutase
Query= metacyc::MONOMER-13382 (455 letters) >lcl|FitnessBrowser__HerbieS:HSERO_RS06955 HSERO_RS06955 phosphoglucosamine mutase Length = 444 Score = 214 bits (546), Expect = 3e-60 Identities = 154/455 (33%), Positives = 225/455 (49%), Gaps = 42/455 (9%) Query: 3 KLFGTFGVRG-IANEKITPEFAMKIGMAFGTLLKR--EGRKKPLVVVGRDTRVSGEMLKE 59 K FGT GVRG + ITP+F M++G A G +L + +G +P V++G+DTR+SG ML+ Sbjct: 4 KYFGTDGVRGRVGVAPITPDFVMRLGYAAGKVLAKAKDGMTRPTVLIGKDTRISGYMLEA 63 Query: 60 ALISGLLSVGCDVIDVGIAPTPAVQWATKHFNADGGAVITASHNPPEYNGIKLLEPNGMG 119 AL +G + G DV G PTPAV + T+ G VI+ASHNP NGIK +G Sbjct: 64 ALEAGFAAAGVDVWLAGPLPTPAVAYLTRALRLSAGVVISASHNPYHDNGIKFFSASGNK 123 Query: 120 LKKEREAIVEELFFKEDFDRAKWYEIGEVRR-EDIIKPYIEAIKSKVDVEAIKKRKPFVV 178 L EA +E ++ D ++G+ RR D YIE KS A+ R +V Sbjct: 124 LPDSVEADIEAA-LEQPMDCVPSEKLGKARRLSDAPGRYIEFCKSTFP-NAMNLRGMRLV 181 Query: 179 VDTSNGAGSLTLPYLLRELGCKVITVNAQPDGYFPARNPEPNEENLKEFMEIVKALGADF 238 VD ++GA P++ ELG +VIT+ QPDG N + K + V+ AD Sbjct: 182 VDCAHGAAYNIAPHVFHELGAEVITIGNQPDGL--NINEDCGATAPKTLVASVREYRADL 239 Query: 239 GVAQDGDADRAVFIDENGRFIQGDKTFALVADAVLKEKGGGLLVTTVATSNLLDDIAKKH 298 G+A DGDADR + +D GR GD+ L+ L V T+ T+ L+ KK Sbjct: 240 GIALDGDADRLIMVDGEGRIYNGDELLYLMVKDRLATGPVHGAVGTLMTNMALEVAFKKM 299 Query: 299 GAKVMRTKVGDLIVARALYENNGTIGGEENGGVI-FPEHVLGRDGAMTVAKVVEIFAKSG 357 G R KVGD V L E +GGE +G ++ +H G DG ++ +V+ +SG Sbjct: 300 GVPFERAKVGDRYVLEVLQEKGWVLGGEGSGHLLALDKHTTG-DGIVSALQVLSALKRSG 358 Query: 358 KKFSELIDELPKY------------YQIKTKRHVEGDRHAIVNKVAEMARERGYTVDTTD 405 K +EL ++ Y Y K+ ++ ++ A+ ++ E R Sbjct: 359 KTLAELTSDISMYPQSLVNVKIPAGYDWKSNTALQAEKAAVEEELGERGR---------- 408 Query: 406 GAKIIFEDGWVLVRASGTEPIIRIFSEAKSKEKAQ 440 VL+R SGTEP+IR+ EA+ + A+ Sbjct: 409 ----------VLLRPSGTEPLIRVMVEAQQADLAR 433 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: 454 Number of extensions: 28 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: 444 Length adjustment: 33 Effective length of query: 422 Effective length of database: 411 Effective search space: 173442 Effective search space used: 173442 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 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