Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate WP_034214464.1 N787_RS12015 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase
Query= BRENDA::P07874 (481 letters) >NCBI__GCF_000747155.1:WP_034214464.1 Length = 467 Score = 568 bits (1463), Expect = e-166 Identities = 278/468 (59%), Positives = 346/468 (73%), Gaps = 6/468 (1%) Query: 1 MIPVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLAFDGMQAPLLVCNKEHR 60 ++PVILSGGSG+RLWPLSR+ YPKQFL L G+DT+ Q T +R+A AP++V N EHR Sbjct: 4 ILPVILSGGSGTRLWPLSREAYPKQFLPLVGEDTMLQATWRRVAGLAGHAPMVVANAEHR 63 Query: 61 FIVQEQLEAQNLASQAILLEPFGRNTAPAVAIAAMKLVAEGRDELLLILPADHVIEDQRA 120 F+V EQL ++LEP GRNTAPA+A+AA++ +AEG D LLL+LP+DHVI D A Sbjct: 64 FMVAEQLREAGAEGATVILEPMGRNTAPAIAVAALEAMAEGEDALLLVLPSDHVIVDVAA 123 Query: 121 FQQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKPDEAR 180 F A+ LA A+ G++V FGI + PETGYGYI+A+ EGV V+ FVEKPD A Sbjct: 124 FHAAVQLARAQADAGKLVTFGIQPTGPETGYGYIKATG-----EGVRAVEKFVEKPDRAT 178 Query: 181 AREFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVNIDAATF 240 A +VA+G YYWNSGMFLFRASRYL EL + DI C L +S+ D D + +D F Sbjct: 179 AEAYVASGQYYWNSGMFLFRASRYLAELGRLKPDILAACRETLVKSKRDEDFIRLDGEAF 238 Query: 241 ECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKGDVLVHDSH 300 CP +SIDYAVMEKT+ A +VPL +GW+DVGSW+++W+V +DA+GN GDV+ Sbjct: 239 AACPSDSIDYAVMEKTADAALVPLDSGWSDVGSWAALWEVSPQDADGNAWHGDVISIGCR 298 Query: 301 NCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRSETQNHCEV 360 N HG +L++++GLEDIVVV+T DA+++ H+DR+Q+VK +V L GRS H +V Sbjct: 299 NSYAHGE-RLIAMVGLEDIVVVDTDDALLVGHRDRIQEVKDIVGSLKRDGRSHATWHRKV 357 Query: 361 YRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTCDDKTFLLT 420 YRPWG+YDS+D G RFQVK ITVKPG LSLQMHHHRAEHWIVVSGTA+VT D+ LLT Sbjct: 358 YRPWGAYDSIDNGERFQVKRITVKPGGTLSLQMHHHRAEHWIVVSGTAKVTRGDEVILLT 417 Query: 421 ENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGR 468 ENQSTYIP+ VHRL NPGK+PLE+IEVQSGSYLGEDDI R EDVYGR Sbjct: 418 ENQSTYIPLGVVHRLENPGKLPLELIEVQSGSYLGEDDIVRFEDVYGR 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: 679 Number of extensions: 33 Number of successful extensions: 3 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: 467 Length adjustment: 33 Effective length of query: 448 Effective length of database: 434 Effective search space: 194432 Effective search space used: 194432 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