Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13); glucose-1-phosphate guanylyltransferase (EC 2.7.7.34); aldose-1-phosphate nucleotidyltransferase (EC 2.7.7.37); mannose-6-phosphate isomerase (EC 5.3.1.8) (characterized)
to candidate WP_087412248.1 BUB52_RS11065 mannose-1-phosphate guanylyltransferase
Query= BRENDA::O58649 (464 letters) >NCBI__GCF_900129655.1:WP_087412248.1 Length = 360 Score = 198 bits (504), Expect = 2e-55 Identities = 124/350 (35%), Positives = 189/350 (54%), Gaps = 28/350 (8%) Query: 4 LILAGGKGTRLWPLSREAMPKQFIKVF-SDRSLFQKTVERALIFSKPKEIFVVTNKEYRF 62 +I+ GG G+R WP SR+ +PKQF+ F + RSL Q+T +R + I VVTN Y Sbjct: 9 VIMGGGIGSRFWPFSRKTLPKQFLDFFGTGRSLLQQTFDRFSKVIPTENILVVTNDLYAD 68 Query: 63 RVLDDLNELGLKVPEENILLEPVGKNTLPAIYWGLKVINDNYGDSVVAVLPSDHAIEVNE 122 V + L EL E ILLEP +NT P I W I ++ + V PSDH I Sbjct: 69 LVKEQLPEL----KPEQILLEPTRRNTAPCIAWAAYHIRALNPNANIVVAPSDHLILKES 124 Query: 123 SYMEAFKKAEKLAEKY--LVTFGIKPTKPHTGYGYIKPGEKIEVEGKVLGYLVDEFKEKP 180 ++ A +K K L+T GIKP +P TGYGYI+ E I+ Y V F EKP Sbjct: 125 EFLSAIEKGLAFVAKSDKLLTLGIKPNRPETGYGYIQIAEHIDSNF----YKVKTFTEKP 180 Query: 181 DLETARKYVENG-YYWNSGMFMFKVSVFMEEARKHSP----------DVVKAFEEGKSIE 229 +LE A+ +VE+G +YWN+G+FM+ V+ ++ P DV EE K I+ Sbjct: 181 ELELAKVFVESGEFYWNAGLFMWNVNSIIKAGESLLPELATKLAAGKDVYGTPEEKKFID 240 Query: 230 EIYELAPEISVDYGIMEKTNKAAVVPLNTYWNDLGSFDAVYEALEKDENGNAVHVTGFKA 289 E + P +S+D+GIMEK + V + W+DLG++ ++Y+ +KDE+ N K Sbjct: 241 ENFPACPNVSIDFGIMEKADNVYVSLGDFGWSDLGTWGSLYDLSQKDESENVT----LKC 296 Query: 290 KYINVDSRNNLVL--TERLTATVGVEDLVIIDTGDALLVAKRGETQKVKE 337 + + +S+NN+V+ +L G+E +I ++ + LL+ K+ E +++ Sbjct: 297 QSLLYNSKNNIVVLPQNKLAVIDGLEGYLIAESDNVLLICKKDEEHSIRK 346 Lambda K H 0.316 0.137 0.395 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: 474 Number of extensions: 32 Number of successful extensions: 8 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: 464 Length of database: 360 Length adjustment: 31 Effective length of query: 433 Effective length of database: 329 Effective search space: 142457 Effective search space used: 142457 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 50 (23.9 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