Align protein-Npi-phosphohistidine-D-glucose phosphotransferase (EC 2.7.1.199) (characterized)
to candidate WP_010529795.1 ON01_RS04430 PTS transporter subunit EIIC
Query= BRENDA::P69786 (477 letters) >NCBI__GCF_000224785.1:WP_010529795.1 Length = 492 Score = 292 bits (748), Expect = 2e-83 Identities = 174/482 (36%), Positives = 269/482 (55%), Gaps = 38/482 (7%) Query: 9 LQKVGKSLMLPVSVLPIAGILLGVGS--ANFSWLPAVVSHVMAEAGG-SVFANMPLIFAI 65 LQ +G+SLMLPV+VLP A IL+G+ A +GG ++ N+ ++FA+ Sbjct: 5 LQNLGRSLMLPVAVLPAAAILVGISKYIEKIDGTTAGTIATFLNSGGLAILDNLGILFAV 64 Query: 66 GVALGFTNN-DGVSALAAVVAYGIMVKTMAVVAPLVLHLPAEEIASKHLADT-GVLGGII 123 GVA+G + DG + L+ +VA+ + ++V L E + + V GI+ Sbjct: 65 GVAIGMSKEQDGAAGLSGLVAWLVATTVLSVSGVAGLQGIEESAVNPAFENIQNVFIGIL 124 Query: 124 SGAIAAYMFNRFYRIKLPEYLGFFAGKRFVPIISGLAAIFTGVVLSFIWPPIGSAIQTFS 183 SG +A+ M+NRF ++LP+ L FF+GKR VPI+S + + V+L F+WP + +A+ +F Sbjct: 125 SGIVASIMYNRFSHVRLPDALAFFSGKRLVPIMSAASMMVVSVLLLFVWPVVYNALVSFG 184 Query: 184 QWAAYQNPVVAFGIYGFIERCLVPFGLHHIWNVPFQMQIGEYTNAAGQVFHGDIPRYMAG 243 + A V GIYGF+ R L+P GLHH N F + DI + A Sbjct: 185 E-AIISLEAVGAGIYGFLNRLLIPTGLHHALNSVFWFDVAGID---------DIASFWAS 234 Query: 244 DPTAGK----LSGGFLFKMYGLPAAAIAIWHSAKPENRAKVGGIMISAALTSFLTGITEP 299 + G L+G F M+GLPAAA+A++H+AK + + + ++++AA SF TG+TE Sbjct: 235 EGEKGVTGRYLAGFFPIMMFGLPAAALAMYHTAKTKRKKQAASLLMAAAFASFFTGVTEA 294 Query: 300 IEFSFMFVAPILYIIHAILAGLAFPICILLGMRDGTSFSHGLIDFIVLSG--NSSKLWLF 357 +EFSFMFVAP+LY++HA L GL+ + + G SFS GL+D+ + G +++ ++ Sbjct: 295 LEFSFMFVAPVLYVVHAALTGLSLAVAAMFEWTAGFSFSAGLVDYTLSLGIPIANQPYML 354 Query: 358 PIVGIGYAIVYYTIFRVLIKALDLKTPGR----------------EDATEDAKATGTSEM 401 + G+ +A++YY +FR LI LDL TPGR E+ T ++ T+ M Sbjct: 355 ILQGLVFAVLYYFLFRFLIVKLDLNTPGRESDEPGEGEVDESYNVEEGTLASEKDETAVM 414 Query: 402 APALVAAFGGKENITNLDACITRLRVSVADVSKVDQAGLKKLGAAGVVVAGS-GVQAIFG 460 A + GG EN+ +D C++RLR+ V D+ KVDQ +K G GV V G VQ + G Sbjct: 415 AEEIYQGLGGDENVRTVDNCVSRLRLEVDDMDKVDQDKIKATGVPGVNVVGKHNVQVVVG 474 Query: 461 TK 462 T+ Sbjct: 475 TQ 476 Lambda K H 0.325 0.140 0.422 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: 658 Number of extensions: 41 Number of successful extensions: 7 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: 477 Length of database: 492 Length adjustment: 34 Effective length of query: 443 Effective length of database: 458 Effective search space: 202894 Effective search space used: 202894 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 bits) S2: 52 (24.6 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