Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_012466687.1 CLIM_RS08945 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_000020465.1:WP_012466687.1 Length = 484 Score = 540 bits (1392), Expect = e-158 Identities = 266/472 (56%), Positives = 339/472 (71%), Gaps = 1/472 (0%) Query: 1 MIPVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRL-AFDGMQAPLLVCNKEH 59 ++PVILSGGSG+RLWPLSR YPKQ L L + T+ Q+T+ RL A D + +CN++H Sbjct: 2 ILPVILSGGSGTRLWPLSRALYPKQLLPLVSERTMLQETVLRLEALDDLGPVCCICNEQH 61 Query: 60 RFIVQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQR 119 RF+V EQ+ + I+LEP GRNTAPA A+AA+ ++ + LLLILPADHVI D+ Sbjct: 62 RFLVAEQMHEVCKSIGGIILEPMGRNTAPAAAVAAIHALSRFENPLLLILPADHVICDRA 121 Query: 120 AFQQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEA 179 AF A+A T+AA G +V FGI + PETGYGYIRA + V FVEKPD A Sbjct: 122 AFAGAVAAGTDAALSGALVTFGIVPTGPETGYGYIRAQREGSGTASCYPVVEFVEKPDLA 181 Query: 180 RAREFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAAT 239 A +++ +G Y+WNSGMFLFRA RYLEEL + + + +C A E++ D D + +D Sbjct: 182 HAEQYIRSGAYFWNSGMFLFRAERYLEELDRTNPAMLASCREAYEKASSDLDFLRLDRDA 241 Query: 240 FECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHDS 299 F CP +SIDYAVMEKTSRA V PL AGWNDVG+WS++W++ D NV KGDVL+HD Sbjct: 242 FGACPGDSIDYAVMEKTSRAVVAPLDAGWNDVGAWSALWELQEHDNAANVVKGDVLLHDV 301 Query: 300 HNCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNHCE 359 N +H +LV+V+GLED +VVET DA+++A +DRVQDVK +V+ L GR E +NH + Sbjct: 302 RNSYIHAASRLVAVVGLEDQIVVETPDAVLVASRDRVQDVKIIVRQLTESGRGEAENHRK 361 Query: 360 VYRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTFLL 419 VYRPWGSY++VD+ RFQVK I VKPGA LSLQ H+HRAEHWIVV GTA +T ++ L Sbjct: 362 VYRPWGSYETVDVADRFQVKRIVVKPGAALSLQKHYHRAEHWIVVKGTALITVGEQEITL 421 Query: 420 TENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGRTAE 471 E+QSTYIP+ +VHRL NPGKIPLE+IEVQ+GSYLGEDDI R+ED YGR+ E Sbjct: 422 GEDQSTYIPLGTVHRLENPGKIPLELIEVQTGSYLGEDDIVRVEDRYGRSGE 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: 702 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: 484 Length adjustment: 34 Effective length of query: 447 Effective length of database: 450 Effective search space: 201150 Effective search space used: 201150 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: 52 (24.6 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