Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_085121227.1 B9O00_RS04385 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_900177295.1:WP_085121227.1 Length = 473 Score = 448 bits (1152), Expect = e-130 Identities = 226/469 (48%), Positives = 310/469 (66%), Gaps = 1/469 (0%) Query: 1 MIPVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLAFDG-MQAPLLVCNKEH 59 + PVILSGGSGSRLWPLSR+ PKQ L L G TL + T++R++ G P LV N EH Sbjct: 4 LYPVILSGGSGSRLWPLSRQSNPKQLLPLVGRQTLLEATLRRVSGSGAFHPPTLVVNAEH 63 Query: 60 RFIVQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQR 119 RF V EQ A +AILLE GRNTAPA+ AA+ L+A ++L+LP+DH+I D + Sbjct: 64 RFAVAEQARLAGTAPRAILLEAVGRNTAPAILCAALDLLAADDSAIMLVLPSDHLIRDAK 123 Query: 120 AFQQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEA 179 AF++A+ A AA G ++ GI RPETGYG+I G V F EKPD A Sbjct: 124 AFRRAVETARAAAAAGRVMTLGITPDRPETGYGWIEKGGALDGLAGAFEVARFKEKPDAA 183 Query: 180 RAREFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAAT 239 A +A G + WN+G+F+ A+R + EL++ + ++ C AL+R+ D D +D + Sbjct: 184 TAAAMLADGRHLWNAGIFVLPAARVVAELERLEPELVQHCRDALDRASKDIDFTRLDPES 243 Query: 240 FECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHDS 299 F SIDYA++E+ R V + GW+D+G + ++++V +D GN T G + D+ Sbjct: 244 FGQAKAISIDYALVERVERVGTVAVEMGWSDLGGFDALYEVAERDEQGNATVGRTALLDA 303 Query: 300 HNCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNHCE 359 +C V NG+LV+V+GLE ++VVET DA+++A + R QDVK +V+ L ++G E + Sbjct: 304 RDCHVRSNGRLVTVLGLEGVLVVETDDAVLVADRGRAQDVKQLVEKLKSEGFPEATQGSK 363 Query: 360 VYRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTFLL 419 +RPWG + ++DMG RFQVK I+V PGA LSLQMHHHRAEHWIVVSGTA+V + ++FLL Sbjct: 364 WHRPWGWFQTLDMGERFQVKRISVNPGASLSLQMHHHRAEHWIVVSGTAEVNRETESFLL 423 Query: 420 TENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGR 468 EN+STYIP+ HRL NPG++ LE+IEVQSG+YLGEDDI R +D YGR Sbjct: 424 AENESTYIPLGQRHRLTNPGRVQLEMIEVQSGAYLGEDDIVRFDDNYGR 472 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: 581 Number of extensions: 20 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: 473 Length adjustment: 33 Effective length of query: 448 Effective length of database: 440 Effective search space: 197120 Effective search space used: 197120 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