Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_085124919.1 B9O00_RS22145 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_900177295.1:WP_085124919.1 Length = 497 Score = 471 bits (1213), Expect = e-137 Identities = 242/472 (51%), Positives = 309/472 (65%), Gaps = 5/472 (1%) Query: 3 PVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLA-FDGMQAPLLVCNKEHRF 61 PV+LSGG+G+RLWPLSRK YPKQ AL D T+ Q+T+ R G+ PL+VC++E RF Sbjct: 26 PVLLSGGAGTRLWPLSRKHYPKQLQALLSDRTMLQETVLRTRDLAGVAPPLVVCHQEQRF 85 Query: 62 IVQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQRAF 121 +V EQL A LA Q I+LEP GRNTAPA+ ++A+ L E LLL PADH I D AF Sbjct: 86 LVTEQLAAVGLAPQRIVLEPSGRNTAPALVVSALLLAGEDPQGLLLAQPADHHIADPEAF 145 Query: 122 QQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEARA 181 + A+A A AA G +V FG+ +RPETGYGYI+A A EGV V SFVEKP+ A A Sbjct: 146 RAAVAQAARAARDGWLVTFGVRPTRPETGYGYIQAGAAIDGFEGVRAVLSFVEKPEAATA 205 Query: 182 REFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAATFE 241 + G YWNSG+FL +L+E+++ D+ C A+ + D + +DA FE Sbjct: 206 ARLAGSPGCYWNSGVFLLPVGPFLDEVRRLQPDLLAACERAIAEGREDLEFFRLDAEAFE 265 Query: 242 CCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWD----VHAKDANGNVTKGDVLVH 297 P ID A+ME + R VVP+ GW DVGSW + + + +++GNV +GDV Sbjct: 266 SAPALPIDKAIMELSGRVAVVPVEMGWRDVGSWPVLHEALRTLRPTESDGNVFEGDVEAE 325 Query: 298 DSHNCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNH 357 NC + +G+LV+ +G+ED+ +V T DA+++A D V +V+ L + R E +H Sbjct: 326 SVRNCHIRADGRLVAALGVEDLTIVVTDDAVLVARTDEAARVGALVERLGRRNRQEVLHH 385 Query: 358 CEVYRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTF 417 VYRPWGSY SVD G RFQVK I VKPGA LSLQMHHHRAEHWIVV GTA+V CD Sbjct: 386 STVYRPWGSYQSVDSGERFQVKRIVVKPGAELSLQMHHHRAEHWIVVRGTARVHCDGDER 445 Query: 418 LLTENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGRT 469 LL ENQSTYIP + HRL+NPG +PL +IEVQSGSYLGEDDI R +D YGR+ Sbjct: 446 LLHENQSTYIPPGTTHRLSNPGILPLHLIEVQSGSYLGEDDIVRFQDSYGRS 497 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: 615 Number of extensions: 29 Number of successful extensions: 4 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: 497 Length adjustment: 34 Effective length of query: 447 Effective length of database: 463 Effective search space: 206961 Effective search space used: 206961 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