Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_037448989.1 N825_RS07085 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_000576635.1:WP_037448989.1 Length = 478 Score = 516 bits (1330), Expect = e-151 Identities = 250/466 (53%), Positives = 323/466 (69%) Query: 3 PVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLAFDGMQAPLLVCNKEHRFI 62 PV+LSGGSGSRLWP+SR+ YPKQ L L G+ T+ Q T+ R+A +G PL++CN EHRF+ Sbjct: 12 PVLLSGGSGSRLWPISRESYPKQLLPLVGERTMLQDTVGRVAGEGFARPLVICNDEHRFV 71 Query: 63 VQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQRAFQ 122 + EQL ++ AI LEP GRNTA A A+AA+ + + D LLL+LPADHVI D AF Sbjct: 72 IAEQLRQISVTPFAIALEPVGRNTAAAAAVAALIIADQDPDALLLLLPADHVIRDPAAFH 131 Query: 123 QALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEARAR 182 A+ A AA G +V FGI ++PETGYGYIR A+ GV V +FVEKP +A Sbjct: 132 AAVETAAGAAAAGNLVTFGITPTQPETGYGYIRQGAELTAHSGVFLVDAFVEKPGIEKAA 191 Query: 183 EFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAATFEC 242 + +AAGG++WN GMFLF A++ L EL+K + I C A+ + D D +D F Sbjct: 192 DMLAAGGHFWNGGMFLFSAAKLLSELEKFEPAIVAACREAIAKGSRDLDFFRLDPDAFGA 251 Query: 243 CPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHDSHNC 302 P SIDYAVME+T A VVP + GW DVG+WS++WD+ AK+ +GNV GDV+ D+ NC Sbjct: 252 APSISIDYAVMERTDSAVVVPANIGWTDVGAWSALWDIGAKNEDGNVFVGDVMTEDAKNC 311 Query: 303 LVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNHCEVYR 362 + G L +V+GL+D+VVV T DA+++A +D+VQD+K +V+ L +GR E + H V+R Sbjct: 312 YIRSEGVLTAVVGLDDVVVVATDDAILVASRDKVQDIKKIVERLKKEGRPEAKIHSRVHR 371 Query: 363 PWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTFLLTEN 422 PWG Y + G RFQVK +TVKPGA LSLQ H+HRAEHW+VV+GTA VT D LL EN Sbjct: 372 PWGFYQCLHEGERFQVKRLTVKPGATLSLQKHYHRAEHWVVVNGTALVTRDADQVLLREN 431 Query: 423 QSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGR 468 +S YIP+ +VHRL NPGK+ L +IEVQSGSYLGEDDI RL D YGR Sbjct: 432 ESIYIPLGAVHRLENPGKVTLNLIEVQSGSYLGEDDIVRLTDTYGR 477 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: 614 Number of extensions: 19 Number of successful extensions: 1 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: 478 Length adjustment: 34 Effective length of query: 447 Effective length of database: 444 Effective search space: 198468 Effective search space used: 198468 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