Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_008509924.1 BIBO1_RS16365 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_000182725.1:WP_008509924.1 Length = 471 Score = 432 bits (1110), Expect = e-125 Identities = 226/475 (47%), Positives = 309/475 (65%), Gaps = 16/475 (3%) Query: 2 IPVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLA-FDGMQAPLLVCNKEHR 60 IPVI+SGGSGSRLWPLSR +PK F+ L +TL +T R + ++ L V N++ Sbjct: 4 IPVIISGGSGSRLWPLSRDAHPKPFIKLPDGETLIGKTYARASRLANVEQILTVTNRDFL 63 Query: 61 FIVQEQLEAQNLASQ--AILLEPFGRNTAPAVAIAAMKLV-AEGRDELLLILPADHVIED 117 F+ + A A LLEP GR+TAPAVA+AA+ A G D LL++PADH+IED Sbjct: 64 FLTLDAYAAAGAAQMENTFLLEPLGRDTAPAVALAALHAAEAYGPDATLLVMPADHLIED 123 Query: 118 QRAFQQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPD 177 ++AF +A+A A AE G +V FGI RPETG+GYI + VQ FVEKPD Sbjct: 124 EQAFAEAVAKARALAEAGRIVTFGIVPDRPETGFGYIEVQG--------TDVQRFVEKPD 175 Query: 178 EARAREFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQ--HDGDLVNI 235 EA A+ +V +G Y+WNSGMF F+AS ++ +++H + AL +++ ++G+ + Sbjct: 176 EATAQTYVESGRYFWNSGMFCFKASSMIDAMQRHAPQVLAGARAALAQARRGNNGETKTL 235 Query: 236 DAAT--FECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGD 293 + A F P SIDYAVMEK VP+S GW+D+GSW+++ D+ D NGN +G+ Sbjct: 236 EIARDEFAATPAISIDYAVMEKADNMACVPVSCGWSDIGSWAAMADLVTPDENGNRLRGE 295 Query: 294 VLVHDSHNCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSE 353 ++ D+ N V +LVS++G+ D++VV+T DA+++AH+D+ Q+V+ V L QG Sbjct: 296 TVLEDTTNSFVLSETRLVSLVGVHDLLVVDTPDALLVAHRDKAQEVRSVFNKLRKQGHEA 355 Query: 354 TQNHCEVYRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCD 413 + H +RPWG+Y ++ G F++K I VKPG RLSLQ HHHR+EHWIVVSGTA+VT Sbjct: 356 AKLHRTAHRPWGTYTVLEEGDGFKIKRIEVKPGRRLSLQAHHHRSEHWIVVSGTAKVTNG 415 Query: 414 DKTFLLTENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGR 468 D+ LLT NQSTYIP HRL NPG +PL +IEVQSG YLGEDDI R +DVYGR Sbjct: 416 DREILLTTNQSTYIPCGFRHRLENPGILPLVLIEVQSGEYLGEDDIVRYDDVYGR 470 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: 632 Number of extensions: 28 Number of successful extensions: 5 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: 471 Length adjustment: 33 Effective length of query: 448 Effective length of database: 438 Effective search space: 196224 Effective search space used: 196224 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