Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_111609056.1 DK187_RS19920 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_003259225.1:WP_111609056.1 Length = 465 Score = 496 bits (1277), Expect = e-145 Identities = 244/468 (52%), Positives = 326/468 (69%), Gaps = 9/468 (1%) Query: 3 PVILSGGSGSRLWPLSRKQYPKQFLALTGD-DTLFQQTIKRLAFDGMQAPLLVCNKEHRF 61 PV+LSGG GSRLWPLSR+ +PKQ L LT +L QQT+ R++ +Q P++VCN +HRF Sbjct: 5 PVVLSGGVGSRLWPLSREHFPKQCLNLTDSLSSLLQQTLARMSHLNVQPPIVVCNDDHRF 64 Query: 62 IVQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLV-AEGRDELLLILPADHVIEDQRA 120 ++ +QL+ + ++LEP GRNTAPAVA+AA +++ ++ D L+L+LPADHVI + A Sbjct: 65 LIAQQLQDMGVKGAKVMLEPVGRNTAPAVALAAFEVLQSDNEDSLMLVLPADHVIRNTAA 124 Query: 121 FQQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEAR 180 F++A+ A A+ G +V FGI +R ETGYGYI+A DA V+ FVEKPD A Sbjct: 125 FEKAIEQAKVLAKAGGLVTFGIKPTRAETGYGYIKAGQDAC-------VEKFVEKPDLAT 177 Query: 181 AREFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAATF 240 A+ ++ +G Y WNSGMFLF+ S+YL ELK++ DIY A D D + I A F Sbjct: 178 AQSYLESGNYLWNSGMFLFQTSQYLAELKQYRPDIYAAVASAYGNRTEDLDFIRIGAEVF 237 Query: 241 ECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHDSH 300 CP SIDYAVME T A VVP + W+D+G+W+++ D KD+N NV GDV+ + Sbjct: 238 TACPSESIDYAVMETTKNAKVVPYAGDWSDIGAWNALHDYSDKDSNHNVLVGDVMAESTT 297 Query: 301 NCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNHCEV 360 N L+ +LV+ +G+ ++VV+ET DA++I KD+ QDVK +V + A+GR E +H V Sbjct: 298 NSLIRAESRLVATVGVNNLVVIETADAVLIMDKDQSQDVKKIVSRIKAEGRQEHMHHTTV 357 Query: 361 YRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTFLLT 420 +RPWG+Y +VD+G R QVK I VKPG +LS+QMHHHRAEHW+VVSGTA+V ++ LLT Sbjct: 358 HRPWGTYQTVDLGDRHQVKRIMVKPGEKLSVQMHHHRAEHWVVVSGTAKVQNGEREILLT 417 Query: 421 ENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGR 468 EN+STYIP+ VH L NPGKIPLE+IEVQSGSYLGEDDI R D YGR Sbjct: 418 ENESTYIPVGVVHALENPGKIPLELIEVQSGSYLGEDDIVRFSDRYGR 465 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: 593 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: 465 Length adjustment: 33 Effective length of query: 448 Effective length of database: 432 Effective search space: 193536 Effective search space used: 193536 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