Align Histidine biosynthesis trifunctional protein; EC 3.5.4.19; EC 3.6.1.31; EC 1.1.1.23 (characterized)
to candidate PP_0966 PP_0966 Histidinol dehydrogenase
Query= SwissProt::P00815 (799 letters) >FitnessBrowser__Putida:PP_0966 Length = 441 Score = 248 bits (632), Expect = 7e-70 Identities = 143/402 (35%), Positives = 230/402 (57%), Gaps = 13/402 (3%) Query: 391 IIENVRDKGNSALLEYTEKFDGV---KLSNPVLNAPFPEEYFEGLTEEMKEALDLSIENV 447 II+ VR++G++AL+E+T++FDGV + + +L+ E +T +EAL+ + V Sbjct: 42 IIKAVRERGDAALVEFTQRFDGVDAKSIDDLILDRARLELALTRITPVQREALEKAANRV 101 Query: 448 RKFHAAQLPTETLEVETQPGVLCSRFPRPIEKVGLYIPGGTAILPSTALMLGVPAQVAQC 507 R +H Q ++ + G + + P+++ GLY+PGG A PS+ LM +PA+VA Sbjct: 102 RIYHERQ-KQDSWQYTEADGTVLGQKVTPLDRAGLYVPGGKASYPSSVLMNAIPAKVAGV 160 Query: 508 KEIVFASPPRKSDGKVSPEVVYVAEKVGASKIVLAGGAQAVAAMAYGTETIPKVDKILGP 567 E+V P + G+V+ V+ A G ++ GGAQAVAA+AYGTE++P+VDKI+GP Sbjct: 161 TEVVMVVPTPR--GEVNELVLAAACIAGVDRVFTVGGAQAVAALAYGTESVPQVDKIVGP 218 Query: 568 GNQFVTAAKMYVQNDTQALCSIDMPAGPSEVLVIADEDADVDFVASDLLSQAEHGIDSQV 627 GN +V AK +V IDM AGPSE+LV+ D D D++A DL SQAEH D+Q Sbjct: 219 GNIYVATAKRHVFGQV----GIDMIAGPSEILVVCDGQTDPDWIAMDLFSQAEHDEDAQA 274 Query: 628 ILVGVNLSEKKIQEIQDAVHNQALQLPRVDIVRKCI-AHSTIVLCDGYEEALEMSNQYAP 686 ILV + + + + ++ + R DI+ K I ++ ++A++++N+ AP Sbjct: 275 ILVSPDAAF--LDRVAASIDKLMPTMERADIIEKSINGRGALIQVRDMQQAMDVANRIAP 332 Query: 687 EHLILQIANANDYVKLVDNAGSVFVGAYTPESCGDYSSGTNHTLPTYGYARQYSGANTAT 746 EHL L +A+ ++ + +AG++F+G +T E+ GDY +G NH LPT G AR S Sbjct: 333 EHLELSVADPQAWLPHIRHAGAIFMGRHTSEALGDYCAGPNHVLPTSGTARFSSPLGVYD 392 Query: 747 FQKFITAQNITPEGLENIGRAVMCVAKKEGLDGHRNAVKIRM 788 FQK + + +G +G +A+ E L H + + R+ Sbjct: 393 FQKRSSIIFCSEQGASELGHTASVLARGESLTAHARSAEYRI 434 Lambda K H 0.315 0.133 0.371 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: 694 Number of extensions: 40 Number of successful extensions: 5 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: 799 Length of database: 441 Length adjustment: 37 Effective length of query: 762 Effective length of database: 404 Effective search space: 307848 Effective search space used: 307848 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 Aug 03 2021. The underlying query database was built on Aug 03 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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