Align Histidine biosynthesis trifunctional protein; EC 3.5.4.19; EC 3.6.1.31; EC 1.1.1.23 (characterized)
to candidate BPHYT_RS17710 BPHYT_RS17710 histidinol dehydrogenase
Query= SwissProt::P00815 (799 letters) >FitnessBrowser__BFirm:BPHYT_RS17710 Length = 440 Score = 239 bits (609), Expect = 3e-67 Identities = 153/441 (34%), Positives = 232/441 (52%), Gaps = 15/441 (3%) Query: 359 LDVVKASDKVGVQKALSRPIQKTSEIMHLVNPIIENVRDKGNSALLEYTEKFDGVKLSN- 417 LD + + L+ + I V I+ +V+ +G++A+LEYT++FD V+ + Sbjct: 8 LDSTAPDFQKSLHAVLAFEASEDEAIERSVAQILNDVKARGDAAVLEYTQRFDRVEAKSV 67 Query: 418 PVLNAPFPE--EYFEGLTEEMKEALDLSIENVRKFHAAQ---LPTETLEVETQPGVLCSR 472 L P E E L + + AL+ + VR +H Q + + + G + + Sbjct: 68 DALELPMSELEAALENLEPKRRAALEAAAARVRGYHEKQKIECGSHSWQYTEADGTVLGQ 127 Query: 473 FPRPIEKVGLYIPGGTAILPSTALMLGVPAQVAQCKEIVFASPPRKSDGKVSPEVVYVAE 532 P+++ G+Y+PGG A PS+ LM +PA+VA +EIV P DG +P V+ A Sbjct: 128 KVTPLDRAGIYVPGGKAAYPSSVLMNAIPARVAGVREIVMVVPT--PDGVKNPLVLAAAL 185 Query: 533 KVGASKIVLAGGAQAVAAMAYGTETIPKVDKILGPGNQFVTAAKMYVQNDTQALCSIDMP 592 G ++ GGAQAV A+AYGT TIP VDKI GPGN +V +AK V IDM Sbjct: 186 LGGVDRVFTIGGAQAVGALAYGTATIPAVDKICGPGNAYVASAKRRVFGTV----GIDMI 241 Query: 593 AGPSEVLVIADEDADVDFVASDLLSQAEHGIDSQVILVGVNLSEKKIQEIQDAVHNQALQ 652 AGPSE+LV+ D D +VA DL SQAEH +Q IL+ + + I ++DA+ Sbjct: 242 AGPSEILVLCDGTTDPRWVAMDLFSQAEHDELAQSILLCPD--DAFIGRVKDAIDELLPT 299 Query: 653 LPRVDIVRKCIA-HSTIVLCDGYEEALEMSNQYAPEHLILQIANANDYVKLVDNAGSVFV 711 +PR D++RK + ++ E+A ++N APEHL + + + +L+ +AG++F+ Sbjct: 300 MPRRDVIRKSLEDRGALIKVRDMEQACAIANDIAPEHLEISALEPHHWGQLIRHAGAIFL 359 Query: 712 GAYTPESCGDYSSGTNHTLPTYGYARQYSGANTATFQKFITAQNITPEGLENIGRAVMCV 771 G YT ES GDY +G NH LPT AR S F K + ++ EG + +G + Sbjct: 360 GRYTSESLGDYCAGPNHVLPTSRTARFSSPLGVYDFFKRSSVIEVSAEGAQTLGEIAAEL 419 Query: 772 AKKEGLDGHRNAVKIRMSKLG 792 A EGL H + + RM + G Sbjct: 420 AYGEGLQAHARSAEYRMRQNG 440 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: 713 Number of extensions: 33 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: 440 Length adjustment: 37 Effective length of query: 762 Effective length of database: 403 Effective search space: 307086 Effective search space used: 307086 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