Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_085641414.1 MGEO_RS19505 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_002115805.1:WP_085641414.1 Length = 475 Score = 412 bits (1060), Expect = e-119 Identities = 211/469 (44%), Positives = 296/469 (63%), Gaps = 4/469 (0%) Query: 3 PVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLAFDGMQAPLLVCNKEHRFI 62 PV+L GGSG+RLWPLSRK YPKQF G ++LFQ+ +R++ D APL V RFI Sbjct: 9 PVLLCGGSGTRLWPLSRKSYPKQFAPFLGKESLFQEAARRVSGDVFAAPLAVTGDGFRFI 68 Query: 63 VQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQRAFQ 122 V EQL+ + IL+EP GRNTAPA A AA+ L L+L++PADH I D +AF+ Sbjct: 69 VAEQLDHCEVRPAGILIEPEGRNTAPAAAAAALHLAETDPGALMLLVPADHAIPDAQAFR 128 Query: 123 QALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEARAR 182 A+ AA++G++V FGI +R ETGYG++ A A+ GV+ ++ F+EKPD A+A Sbjct: 129 DAVMTGAVAADQGQIVTFGIQPTRAETGYGWLEAGAETH--PGVNALERFIEKPDAAKAE 186 Query: 183 EFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAATFEC 242 A Y WN+G+FL RA + + H DI D A++ ++ D + ID + Sbjct: 187 TLFADDRYLWNAGLFLTRADTLIAAFEAHAPDILDATRAAMQAAKTDLGFLRIDPDLWGQ 246 Query: 243 CPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHDSHNC 302 SIDYAVME+ +V ++GW+D+GSW ++W +DA+GN G D N Sbjct: 247 VRAESIDYAVMEQAKNVSLVRFASGWSDLGSWEAVWQESPRDADGNAMAGLSTAIDCENT 306 Query: 303 LVHGNGKLVSV--IGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNHCEV 360 L+ + + IGL+++V V +DA+++A Q V+ V L+A+G + Sbjct: 307 LLRSESNEIELVGIGLKNVVAVAMRDAVLVADLTDSQSVRRAVDTLNARGAKQAVQLPVD 366 Query: 361 YRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTFLLT 420 +RPWG ++++ + RFQVK I V PGA LSLQ H HR+EHWIVV+GTA+VT DD+ LLT Sbjct: 367 HRPWGWFETLILADRFQVKRIHVHPGAALSLQSHVHRSEHWIVVAGTAKVTVDDEVRLLT 426 Query: 421 ENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGRT 469 ENQS YIP+ +VHR+ NPGK+P+ +IEVQ+G+YLGEDDI R ED+Y R+ Sbjct: 427 ENQSVYIPLGAVHRMENPGKVPMVLIEVQTGTYLGEDDIIRYEDIYARS 475 Lambda K H 0.319 0.134 0.400 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: 571 Number of extensions: 18 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: 481 Length of database: 475 Length adjustment: 34 Effective length of query: 447 Effective length of database: 441 Effective search space: 197127 Effective search space used: 197127 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 (21.8 bits) S2: 51 (24.3 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