Align Histidine biosynthesis trifunctional protein; EC 3.5.4.19; EC 3.6.1.31; EC 1.1.1.23 (characterized)
to candidate Pf1N1B4_1066 Histidinol dehydrogenase (EC 1.1.1.23)
Query= SwissProt::P00815 (799 letters) >lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1066 Histidinol dehydrogenase (EC 1.1.1.23) Length = 441 Score = 250 bits (639), Expect = 1e-70 Identities = 145/403 (35%), Positives = 232/403 (57%), Gaps = 15/403 (3%) Query: 391 IIENVRDKGNSALLEYTEKFDGVKLSNPVLNAPFPEEYFE----GLTEEMKEALDLSIEN 446 II+ VR++G++AL+E+T+KFDG+++++ + + P E E +T +EAL+ + Sbjct: 42 IIKAVRERGDAALVEFTQKFDGLQVAS-MADLILPRERLELALTRITAPQREALEKAATR 100 Query: 447 VRKFHAAQLPTETLEVETQPGVLCSRFPRPIEKVGLYIPGGTAILPSTALMLGVPAQVAQ 506 VR +H Q E VL + P+++ GLY+PGG A PS+ LM +PA+VA Sbjct: 101 VRSYHEKQKQDSWSYTEADGTVLGQKVT-PLDRAGLYVPGGKASYPSSVLMNAIPAKVAG 159 Query: 507 CKEIVFASPPRKSDGKVSPEVVYVAEKVGASKIVLAGGAQAVAAMAYGTETIPKVDKILG 566 E+V P + G+++ V+ A G ++ GGAQAVAA+AYGTE++PKVDK++G Sbjct: 160 VSEVVMVVPTPR--GEINELVLAAACIAGVDRVFTIGGAQAVAALAYGTESVPKVDKVVG 217 Query: 567 PGNQFVTAAKMYVQNDTQALCSIDMPAGPSEVLVIADEDADVDFVASDLLSQAEHGIDSQ 626 PGN +V AK +V IDM AGPSE+LV+ D D D++A DL SQAEH D+Q Sbjct: 218 PGNIYVATAKRHVFGQV----GIDMIAGPSEILVVCDGQTDPDWIAMDLFSQAEHDEDAQ 273 Query: 627 VILVGVNLSEKKIQEIQDAVHNQALQLPRVDIVRKCI-AHSTIVLCDGYEEALEMSNQYA 685 ILV + + + ++ ++ + R +I+ I ++ E+A+E++N+ A Sbjct: 274 AILVSPDA--EFLDKVAASIAKLLPTMERAEIIETSINGRGALIKVRDMEQAIEVANRIA 331 Query: 686 PEHLILQIANANDYVKLVDNAGSVFVGAYTPESCGDYSSGTNHTLPTYGYARQYSGANTA 745 PEHL L +A+ ++ + +AG++F+G +T E+ GDY +G NH LPT G AR S Sbjct: 332 PEHLELSVADPQAWLPQIRHAGAIFMGRHTSEALGDYCAGPNHVLPTSGTARFSSPLGVY 391 Query: 746 TFQKFITAQNITPEGLENIGRAVMCVAKKEGLDGHRNAVKIRM 788 FQK + + +G +G+ +A+ E L H + + R+ Sbjct: 392 DFQKRSSIIFCSEQGASELGKTASVLARGESLTAHARSAEYRI 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: 737 Number of extensions: 38 Number of successful extensions: 6 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