Align Multiphosphoryl transfer protein; MTP; Diphosphoryl transfer protein; DTP; Phosphotransferase FPr protein; Pseudo-HPr (characterized)
to candidate WP_104485039.1 UN63_RS01625 phosphoenolpyruvate--protein phosphotransferase
Query= SwissProt::P69811 (376 letters) >NCBI__GCF_002936955.1:WP_104485039.1 Length = 949 Score = 236 bits (602), Expect = 2e-66 Identities = 146/378 (38%), Positives = 208/378 (55%), Gaps = 11/378 (2%) Query: 1 MFQLSVQDIHPGEKAGDKEEAIRQVAAALVQAGNVAEGYVNGMLAREQQTSTFLGNGIAI 60 MF L+ QD+ G DK I+ +A L Q G+VA GY GML RE Q ST+LG GIAI Sbjct: 1 MFSLTAQDVKTGVPLADKAAVIQALADWLEQDGHVAAGYGAGMLTREAQNSTYLGQGIAI 60 Query: 61 PHGTTDTRDQVLKTGVQVFQFPEGVTWGDGQVAYVAIGIAASSDEHLGLLRQLTHVLSDD 120 PHGT + R + TG++ P+GV WG G+ AY+ +GIAA SDEHL LL+QL LS D Sbjct: 61 PHGTQECRHLIKNTGIKAMHLPDGVPWGGGERAYLVLGIAAGSDEHLDLLKQLARTLSRD 120 Query: 121 SVAEQLKSATTAEELRALLMGEKQSEQLKLDNEMLTLDIVA----SDLLTLQALNAARLK 176 + E++K+A ++E+ LL G +E +L+ D VA + L L AA L Sbjct: 121 GLFERVKAARQSQEVLQLLQG--NAESATETKFVLSADRVAVKARAGTLELLVEQAATLM 178 Query: 177 EAGAVDATFVTKAINEQPLNLGQGIWLSDSAEGNLRSAIAVSRAANAFDVDGETAAMLVS 236 + + + + ++ + +GQG WL + A ++ A+ + + L++ Sbjct: 179 QLNPTEESALQQSAG---MYIGQGWWLKQIPADDKPGAALLT--ASGITHRQQPVSGLLA 233 Query: 237 VAMNDDQPIAVLKRLADLLLDNKADRLLKADAATLLALLTSDDAPTDDVLSAEFVVRNEH 296 +A+ + +L R+AD L + L D+A L + + VVRN H Sbjct: 234 LAVRGSEHKTLLTRVADWLAAGRGAELAGQDSAEALLNVLKRGPVSLSSHQRTVVVRNTH 293 Query: 297 GLHARPGTMLVNTIKQFNSDITVTNLDGTGKPANGRSLMKVVALGVKKGHRLRFTAQGAD 356 GLHARPG MLV K F++DI V NLDG + +SLMK++ LGVK GH+L F A+G D Sbjct: 294 GLHARPGAMLVQAAKNFDADIQVCNLDGDEHWVSAKSLMKMIGLGVKAGHQLVFRAEGPD 353 Query: 357 AEQALKAIGDAIAAGLGE 374 AE AL A+ +A+ GLGE Sbjct: 354 AEAALDALTEAVNGGLGE 371 Lambda K H 0.314 0.130 0.353 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: 749 Number of extensions: 33 Number of successful extensions: 2 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: 376 Length of database: 949 Length adjustment: 37 Effective length of query: 339 Effective length of database: 912 Effective search space: 309168 Effective search space used: 309168 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: 42 (22.0 bits) S2: 53 (25.0 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