Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_011912351.1 PST_RS05950 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_000013785.1:WP_011912351.1 Length = 481 Score = 786 bits (2030), Expect = 0.0 Identities = 381/473 (80%), Positives = 419/473 (88%), Gaps = 2/473 (0%) Query: 1 MIPVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLAFDGMQAPLLVCNKEHR 60 MIPVILSGGSGSRLWPLSRK +PKQFLALTG+ TLFQQT++RLAFDGMQ PLLVCNK+HR Sbjct: 1 MIPVILSGGSGSRLWPLSRKSFPKQFLALTGEQTLFQQTVERLAFDGMQQPLLVCNKDHR 60 Query: 61 FIVQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQRA 120 FIV+EQL A+ L Q +LLEPFGRNTAPA+ IAAMKL+ EGRDELLL+LPADHVIEDQ+A Sbjct: 61 FIVKEQLAARKLDVQGLLLEPFGRNTAPAIGIAAMKLIEEGRDELLLVLPADHVIEDQKA 120 Query: 121 FQQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQ--LPEGVSRVQSFVEKPDE 178 FQ++LALATNAAE GEMVLFG+P +RPETGYGYIR S DA LP+G+ RV FVEKPDE Sbjct: 121 FQRSLALATNAAENGEMVLFGVPPTRPETGYGYIRGSQDANTGLPDGIKRVAQFVEKPDE 180 Query: 179 ARAREFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAA 238 ARA+ ++ +G YYWNSGMFLFRAS +L+ELKKHD DIYDTC +ALERS +GD V ID A Sbjct: 181 ARAQSYLGSGDYYWNSGMFLFRASVFLDELKKHDPDIYDTCWVALERSVKNGDEVLIDPA 240 Query: 239 TFECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHD 298 TF CCPDNSIDYAVMEKT ACVVP+SAGW+DVGSWSSIWDVH KD NGNV KGDV+ D Sbjct: 241 TFACCPDNSIDYAVMEKTQLACVVPMSAGWSDVGSWSSIWDVHEKDQNGNVLKGDVIAED 300 Query: 299 SHNCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNHC 358 S NCLVHGNGKLV+V+GLEDIVVVETKDAMM+AHKD+VQDVK +V LDAQ RSET+NHC Sbjct: 301 SRNCLVHGNGKLVTVLGLEDIVVVETKDAMMVAHKDKVQDVKKLVSKLDAQERSETKNHC 360 Query: 359 EVYRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTFL 418 VYRPWG YDSVDMGGRFQVK I V PGA LSLQMHHHRAEHWIVVSGTAQVTC+DKTFL Sbjct: 361 AVYRPWGWYDSVDMGGRFQVKRICVNPGASLSLQMHHHRAEHWIVVSGTAQVTCNDKTFL 420 Query: 419 LTENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGRTAE 471 LTENQSTYIPI SVHRLANPGKIPLEIIEVQSGSYLGEDDIER +DVYGR + Sbjct: 421 LTENQSTYIPITSVHRLANPGKIPLEIIEVQSGSYLGEDDIERFDDVYGRAEQ 473 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: 801 Number of extensions: 25 Number of successful extensions: 2 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: 481 Length adjustment: 34 Effective length of query: 447 Effective length of database: 447 Effective search space: 199809 Effective search space used: 199809 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 Apr 09 2024. 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