Align Histidine biosynthesis trifunctional protein; EC 3.5.4.19; EC 3.6.1.31; EC 1.1.1.23 (characterized)
to candidate SMa0398 SMa0398 histidinol dehydrogenase
Query= SwissProt::P00815 (799 letters) >lcl|FitnessBrowser__Smeli:SMa0398 SMa0398 histidinol dehydrogenase Length = 456 Score = 199 bits (505), Expect = 4e-55 Identities = 136/417 (32%), Positives = 196/417 (47%), Gaps = 13/417 (3%) Query: 374 LSRPIQKTSEIMHLVNPIIENVRDKGNSALLEYTEKFDGVKLSNPVLNAPFPE--EYFEG 431 L R S + V PI+E VR +G+ AL + + D ++ L E F+ Sbjct: 35 LRRSETDISGFIEKVAPILEAVRTEGDKALARFGRELDKADVTEANLKVTAAEFDAAFKL 94 Query: 432 LTEEMKEALDLSIENVRKFHAAQLPTETLEVETQPGVLCSRFPRPIEKVGLYIPGGTAIL 491 + + E++ I+N+RKFH Q P E +PG PI+ V LY+P G Sbjct: 95 VDASVLESVQFGIDNIRKFHEEQKPEAMWLKEIRPGAFAGDRFTPIQSVALYVPRGKGSF 154 Query: 492 PSTALMLGVPAQVAQCKEIVFASPPRKSDGKVSPEVVYVAEKVGASKIVLAGGAQAVAAM 551 PS +M VPA VA + +PP DG V + A G + AGGAQAVAA+ Sbjct: 155 PSVTMMTSVPAVVAGVPNLAIVTPP-APDGSVDAATLVAARLAGVETVYKAGGAQAVAAV 213 Query: 552 AYGTETIPKVDKILGPGNQFVTAAKMYVQNDTQALCSIDMPAGPSEVLVIADEDADVDFV 611 AYGTET+ KI+GPG+ +V AAK + +PAGPSEV+++AD+ Sbjct: 214 AYGTETVKPALKIVGPGSPWVVAAK----RSLSGVIDTGLPAGPSEVMILADDTVHGGLA 269 Query: 612 ASDLLSQAEHGIDSQVILV--GVNLSEKKIQEIQDAVHNQALQLPRVDIVRKCIAHST-- 667 A DLL +AEHG DS LV ++E+ + + + H + R + ++ T Sbjct: 270 ALDLLIEAEHGPDSSAYLVTHSGRVAEEALAALPE--HWARMTEQRTAFSKTVLSGKTGG 327 Query: 668 IVLCDGYEEALEMSNQYAPEHLILQIANANDYVKLVDNAGSVFVGAYTPESCGDYSSGTN 727 IVL EE+ E N YAPEHL L ++ + A + +G +TP S ++S G N Sbjct: 328 IVLTSSIEESYEFVNAYAPEHLELLSEQPFIHLGHITEASEILMGTHTPVSIANFSLGPN 387 Query: 728 HTLPTYGYARQYSGANTATFQKFITAQNITPEGLENIGRAVMCVAKKEGLDGHRNAV 784 LPT +AR + + F K + +T R +A EG H AV Sbjct: 388 AVLPTSRWARTFGPLSVTDFVKRSSIGYVTAPAYPEFARHSHNLAIYEGFSSHALAV 444 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: 700 Number of extensions: 33 Number of successful extensions: 4 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: 456 Length adjustment: 37 Effective length of query: 762 Effective length of database: 419 Effective search space: 319278 Effective search space used: 319278 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 preprint 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