Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13); glucose-1-phosphate guanylyltransferase (EC 2.7.7.34); aldose-1-phosphate nucleotidyltransferase (EC 2.7.7.37); mannose-6-phosphate isomerase (EC 5.3.1.8) (characterized)
to candidate WP_068217965.1 AWW68_RS06225 mannose-1-phosphate guanylyltransferase
Query= BRENDA::O58649 (464 letters) >NCBI__GCF_001592965.1:WP_068217965.1 Length = 356 Score = 196 bits (499), Expect = 8e-55 Identities = 126/363 (34%), Positives = 192/363 (52%), Gaps = 39/363 (10%) Query: 4 LILAGGKGTRLWPLSREAMPKQFIKVF-SDRSLFQKTVERALIFSKPKEIFVVTNKEYRF 62 +I+AGG G+R WP SR PKQF+ V + RSL Q T +R L I+V+TNK Y Sbjct: 7 VIMAGGIGSRFWPYSRANKPKQFLDVLGTGRSLIQMTYDRFLNICPSSNIYVITNKSYYD 66 Query: 63 RVLDDLNELGLKVPEENILLEPVGKNTLPAIYWGLKVINDNYGDSVVAVLPSDHAI---E 119 V + L EL ++ ILLEP+G+NT A+ + I + V+ V PSDH + Sbjct: 67 LVKEQLPELS----DDQILLEPIGRNTAAAVAYPAFKIKQRDPEGVMIVAPSDHVVFKDN 122 Query: 120 VNESYMEAFKKAEKLAEKYLVTFGIKPTKPHTGYGYIK----PGEKIEVEGKVLGYLVDE 175 + E + A K ++K L+T GI P++P TGYGYI+ P EK++ V Sbjct: 123 IFEQNLTTAIDAAKGSQK-LITLGIVPSRPETGYGYIQYHSSPQEKVKK--------VKT 173 Query: 176 FKEKPDLETARKYVENG-YYWNSGMFMFKVSVFMEEARKHSPDVVKAFEEGKS------- 227 F EKP+LE A+K++E+G + WN+G+F++ + + ++ DV FEEG Sbjct: 174 FTEKPELELAQKFIESGDFVWNAGIFIWSIDTITKAFHRYLKDVAVIFEEGNDKYYTSDE 233 Query: 228 ---IEEIYELAPEISVDYGIMEKTNKAAVVPLNTYWNDLGSFDAVYEALEKDENGNAVHV 284 I+E Y IS+DYG+MEK +V W+DLGS+D+++E +KD+N N V Sbjct: 234 QSFIDEAYAQCKSISIDYGLMEKAEDVYMVKGEFDWSDLGSWDSLHETKDKDKNNNVVDA 293 Query: 285 TGFKAKYINVDSRNNLVL--TERLTATVGVEDLVIIDTGDALLVAKRGETQKVKEVYKKL 342 T + DS+N V E L ++ +I + + +L+ K+ +K +E Sbjct: 294 TA-----LLYDSKNCYVKGPKETLIVAQDLDGYLITQSDNVILICKKDAEKKFREFLSDA 348 Query: 343 KEE 345 KE+ Sbjct: 349 KEK 351 Lambda K H 0.316 0.137 0.395 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: 434 Number of extensions: 23 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: 464 Length of database: 356 Length adjustment: 31 Effective length of query: 433 Effective length of database: 325 Effective search space: 140725 Effective search space used: 140725 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: 50 (23.9 bits)
This GapMind analysis is from Sep 24 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:
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