Align protein-Npi-phosphohistidine-N-acetyl-D-glucosamine phosphotransferase (EC 2.7.1.193) (characterized)
to candidate WP_019617215.1 G327_RS0123280 PTS transporter subunit EIIC
Query= BRENDA::P45604 (651 letters) >NCBI__GCF_000381745.1:WP_019617215.1 Length = 494 Score = 451 bits (1161), Expect = e-131 Identities = 234/497 (47%), Positives = 326/497 (65%), Gaps = 47/497 (9%) Query: 6 FFQRLGRALQLPIAVLPVAALLLRFGQPDLLNVPFIAQAGGAIFDNLALIFAIGVASSWS 65 +FQRLG+AL LPIA LP+AA+LLRFGQPDLL++ FIA AG +IF NL L+FA+G++ S Sbjct: 4 YFQRLGKALMLPIATLPIAAILLRFGQPDLLDITFIATAGSSIFSNLPLLFALGISVGLS 63 Query: 66 KDNAGSAALAGAVGYFVMTKAMVTINPEINMGVLAGIITGLVAGAVYNRWAGIKLPDFLS 125 KD +G+AALAG +GYFV+T+A + INPE+ +G AGII G+++G YNR+ ++LPDFL+ Sbjct: 64 KDGSGAAALAGVIGYFVLTEATIVINPEVRLGFFAGIIAGIISGHAYNRFYQVRLPDFLA 123 Query: 126 FFGGKRFVPIATGFFCLILAAIFGYVWPPVQHAIHSGGEWIVSAGALGSGIFGFINRLLI 185 FF GKR PI +G CL+ A I G VW VQ+AI + W+ G++G I+G +NR LI Sbjct: 124 FFAGKRLTPIMSGLLCLVAAFICGEVWMYVQNAIDAFSHWVSQGGSIGHFIYGIMNRALI 183 Query: 186 PTGLHQVLNTIAWFQIGE--------------------------------------FTNA 207 P GLH L+++ WF +GE T+ Sbjct: 184 PFGLHYFLHSVFWFSLGECVKVGYEVASSLQEVCLAPELVSSLSIGQVIPNIDGSTITSI 243 Query: 208 AGTVFHGDINRFYAGDGTAGMFMSGFFPIMMFGLPGAALAMYLAAPKARRPMVGGMLLSV 267 A GD+NRF++GD TAG++M+ FP+MM GLPGAA+AMYLA PK R +V GMLLS+ Sbjct: 244 AQDAARGDLNRFFSGDDTAGVYMAWAFPVMMGGLPGAAVAMYLATPKNERKLVAGMLLSL 303 Query: 268 AITAFLTGVTEPLEFLFLFLAPLLYLLHAVLTGISLFIATALGIHAGFSFSAGAIDYVLM 327 T+FLTG+TEPLEF FLF+AP LY++HAV +G+++ I ++GI GF FSAGAID+VL Sbjct: 304 GFTSFLTGITEPLEFSFLFIAPALYVMHAVFSGLAVIITNSMGILHGFGFSAGAIDFVLN 363 Query: 328 YSLPAASKNVWMLLVMGVVFFFVYFLLFSAVIRMFNLKTPGREDKAADVVTEEANSNTEE 387 + L A+K + L+ + + +FF+Y + F A I++F L TP A+ EE N + Sbjct: 364 WGL--ATKPL-ALIPLIIAYFFLYAVTFYAAIKIFKLSTPA---PPAETTDEEGNKVASK 417 Query: 388 GLTQLATSYIAAVGGTDNLKAIDACITRLRLTVGDSAKVNDAACKRLGASGVVKLNKQTI 447 + ++I A+GG +N+K +DACITRLRLTV DS ++ K+LGA GV+K+ Sbjct: 418 ---EKPEAFIQALGGAENIKHVDACITRLRLTVVDSCCFDEDKLKQLGAMGVLKIGDNGA 474 Query: 448 QVIVGAKAESIGDEMKK 464 QVI+G +AES+ +K+ Sbjct: 475 QVILGPRAESVATSIKQ 491 Lambda K H 0.323 0.138 0.406 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: 795 Number of extensions: 44 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 651 Length of database: 494 Length adjustment: 36 Effective length of query: 615 Effective length of database: 458 Effective search space: 281670 Effective search space used: 281670 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.5 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (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