Align phosphomannose mutase (EC 5.4.2.8) (characterized)
to candidate 5210391 Shew_2832 phosphoglucosamine mutase (RefSeq)
Query= metacyc::MONOMER-13382 (455 letters) >FitnessBrowser__PV4:5210391 Length = 443 Score = 211 bits (538), Expect = 3e-59 Identities = 154/460 (33%), Positives = 235/460 (51%), Gaps = 29/460 (6%) Query: 1 MGKLFGTFGVRG-IANEKITPEFAMKIGMAFGTLLKREGRKKPLVVVGRDTRVSGEMLKE 59 M K FGT G+RG + K+TPE A+K+G A G +L R G KK V++G+DTR+SG + + Sbjct: 1 MRKFFGTDGIRGKVGAGKMTPELALKLGWAAGRVLSRTGTKK--VIIGKDTRISGYLFES 58 Query: 60 ALISGLLSVGCDVIDVGIAPTPAVQWATKHFNADGGAVITASHNPPEYNGIKLLEPNGMG 119 A+ +GL + G +V+ +G PTPAV + T+ F A+ G VI+ASHNP NGIK +G Sbjct: 59 AMEAGLSAAGLNVMLMGPMPTPAVAYLTRTFRAEAGVVISASHNPYYDNGIKFFSTDGSK 118 Query: 120 LKKEREAIVEELFFKEDFDRAKWYEIGEVRR-EDIIKPYIEAIKSKVDVE-AIKKRKPFV 177 L E E +E ++ + + + +G+V R ED YIE K E + K + Sbjct: 119 LDDEVELEIER-ELEKPLECVESHLLGKVSRIEDAAGRYIEYCKGNFPAEHTLNGLK--I 175 Query: 178 VVDTSNGAGSLTLPYLLRELGCKVITVNAQPDGYFPARNPEPNEENLKEFMEIVKALGAD 237 VVD ++GA P + RELG +VIT+ +PDG N E ++ + E V A AD Sbjct: 176 VVDCAHGATYHIAPSVFRELGAEVITIGDKPDGI--NINHEVGATSMGKIRETVIAEKAD 233 Query: 238 FGVAQDGDADRAVFIDENGRFIQGDK-TFALVADAVLKEKGGGLLVTTVATSNLLDDIAK 296 G+A DGD DR + ++ +G+ I GD+ + L DA + G +V T+ ++ LD K Sbjct: 234 LGIALDGDGDRIMMVNRHGKVIDGDEILYILACDAQDRGVLKGGVVGTLMSNLGLDLALK 293 Query: 297 KHGAKVMRTKVGDLIVARALYENNGTIGGEENGGVIFPEHVLGRDGAMTVAKVVEIFAKS 356 R+KVGD V L E + IGGE +G ++ +H DG + V+ + Sbjct: 294 ARDIPFARSKVGDRYVMELLKEKDWRIGGENSGHILNLDHGTTGDGIVAGILVLAAMCRK 353 Query: 357 GKKFSELIDELPKYYQIKTKRHVEG-----DRHAIVNKVAEMARERGYTVDTTDGAKIIF 411 EL + + Q+ EG + ++++ AE+ + G Sbjct: 354 QATLEELTEGIKMLPQVLVNVRFEGTHNPLEADSVLSAQAEVEAKLG------------- 400 Query: 412 EDGWVLVRASGTEPIIRIFSEAKSKEKAQEYLNLGIELLE 451 E G VL+R SGTEP+IR+ E + + N E ++ Sbjct: 401 ERGRVLLRKSGTEPLIRVMVEGDVASDVKAHANYIAEAIK 440 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: 519 Number of extensions: 30 Number of successful extensions: 7 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: 443 Length adjustment: 33 Effective length of query: 422 Effective length of database: 410 Effective search space: 173020 Effective search space used: 173020 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