Align phosphomannomutase (EC 5.4.2.8) (characterized)
to candidate Ac3H11_2215 Phosphomannomutase (EC 5.4.2.8)
Query= BRENDA::P26276 (463 letters) >lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_2215 Phosphomannomutase (EC 5.4.2.8) Length = 462 Score = 509 bits (1310), Expect = e-149 Identities = 258/439 (58%), Positives = 324/439 (73%), Gaps = 8/439 (1%) Query: 12 SIFRAYDIRGVVGDTLTAETAYWIGRAIGSESLARGEPCVAVGRDGRLSGPELVKQLIQG 71 +IF+AYDIRG+V TL E A +GRA G+ + A G+ VAVGRDGRLSGP + LIQG Sbjct: 6 AIFKAYDIRGIVPSTLNEEVALGLGRAFGTAARAEGQTTVAVGRDGRLSGPAMSAALIQG 65 Query: 72 LVDCGCQVSDVGMVPTPVLYYAANVLEGKSGVMLTGSHNPPDYNGFKIVVAGETLANEQI 131 LV+ G +V DVG+V TP+LY+AA+ L SG+ +TGSHNP DYNGFK+V+ G + E+I Sbjct: 66 LVEAGIEVIDVGLVTTPLLYFAASTL-CNSGIQVTGSHNPKDYNGFKMVLNGRAIYGEEI 124 Query: 132 QALRERIEKND--LASGVGSVEQVDILPRYFKQIRDDIAMAKPMKVVVDCGNGVAGVIAP 189 Q LR +E+ LA G GSV VD+LP Y ++I D+ +A+PMK+VVDCGNG+AG AP Sbjct: 125 QGLRRTMEQESWQLAPG-GSVRHVDVLPTYRERIVGDVKLARPMKIVVDCGNGIAGASAP 183 Query: 190 QLIEALGCSVIPLYCEVDGNFPNHHPDPGKPENLKDLIAKVKAENADLGLAFDGDGDRVG 249 + ALGC VI L+ EVDGNFPNHHPDP KPENL+DLI +KA +A+LGLAFDGDGDR+G Sbjct: 184 AIFRALGCEVIELFSEVDGNFPNHHPDPSKPENLRDLIDALKASDAELGLAFDGDGDRLG 243 Query: 250 VVTNTGTIIYPDRLLMLFAKDVVSRNPGADIIFDVKCTRRLIALISGYGGRPVMWKTGHS 309 +VT GT I+PDR +MLFA+DV+SR PG +IIFDVKCT+RL I+ GG PVM+KTGHS Sbjct: 244 IVTKDGTNIFPDRQMMLFAQDVLSRVPGGEIIFDVKCTQRLAPAIAAAGGVPVMFKTGHS 303 Query: 310 LIKKKMKETGALLAGEMSGHVFFKERWFGFDDGIYSAARLLEILSQDQRDSEHVFSAFPS 369 LIK +MKET + L GEMSGH+FFKERW+GFDDG Y+ RLLEILS+ Q D V +A P+ Sbjct: 304 LIKARMKETNSPLGGEMSGHIFFKERWYGFDDGTYAGCRLLEILSKSQ-DPSAVLNALPT 362 Query: 370 DISTPEINITVTEDSKF---AIIEALQRDAQWGEGNITTLDGVRVDYPKGWGLVRASNTT 426 STPE+N+ E A ++AL ++T+DG+RVD+P G+GL+RASNTT Sbjct: 363 SFSTPELNVACAEGEPHRLTAELQALAAGQFAAPATVSTIDGLRVDWPDGFGLIRASNTT 422 Query: 427 PVLVLRFEADTEEELERIK 445 PVLVLRFE T E L RI+ Sbjct: 423 PVLVLRFEGHTPEALARIE 441 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: 630 Number of extensions: 23 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: 463 Length of database: 462 Length adjustment: 33 Effective length of query: 430 Effective length of database: 429 Effective search space: 184470 Effective search space used: 184470 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