Align Histidine biosynthesis trifunctional protein; EC 3.5.4.19; EC 3.6.1.31; EC 1.1.1.23 (characterized)
to candidate 16128 b2020 histidinol dehydrogenase (NCBI)
Query= SwissProt::P00815 (799 letters) >FitnessBrowser__Keio:16128 Length = 434 Score = 361 bits (926), Expect = e-104 Identities = 197/423 (46%), Positives = 271/423 (64%), Gaps = 12/423 (2%) Query: 371 QKALSRPIQKTSE-IMHLVNPIIENVRDKGNSALLEYTEKFDGVKLSNPVLNAPFPEEYF 429 ++ L RP SE I VN I++NV+ +G+ AL EY+ KFD ++ ++A Sbjct: 18 RQLLMRPAISASESITRTVNDILDNVKARGDEALREYSAKFDKTTVTALKVSAEEIAAAS 77 Query: 430 EGLTEEMKEALDLSIENVRKFHAAQ-LPTETLEVETQPGVLCSRFPRPIEKVGLYIPGGT 488 E L++E+K+A+ ++++N+ FH AQ LP ++VETQPGV C + RP+ VGLYIPGG+ Sbjct: 78 ERLSDELKQAMAVAVKNIETFHTAQKLPP--VDVETQPGVRCQQVTRPVASVGLYIPGGS 135 Query: 489 AILPSTALMLGVPAQVAQCKEIVFASPPRKSDGKVSPEVVYVAEKVGASKIVLAGGAQAV 548 A L ST LML PA +A CK++V SPP +D E++Y A+ G + GGAQA+ Sbjct: 136 APLFSTVLMLATPASIAGCKKVVLCSPPPIAD-----EILYAAQLCGVQDVFNVGGAQAI 190 Query: 549 AAMAYGTETIPKVDKILGPGNQFVTAAKMYVQNDTQALCSIDMPAGPSEVLVIADEDADV 608 AA+A+GTE++PKVDKI GPGN FVT AK V +IDMPAGPSEVLVIAD A Sbjct: 191 AALAFGTESVPKVDKIFGPGNAFVTEAKRQVSQRLDG-AAIDMPAGPSEVLVIADSGATP 249 Query: 609 DFVASDLLSQAEHGIDSQVILVGVNLSEKKIQEIQDAVHNQALQLPRVDIVRKCIAHSTI 668 DFVASDLLSQAEHG DSQVIL+ + + + +AV Q +LPR + R+ + S + Sbjct: 250 DFVASDLLSQAEHGPDSQVILL--TPAADMARRVAEAVERQLAELPRAETARQALNASRL 307 Query: 669 VLCDGYEEALEMSNQYAPEHLILQIANANDYVKLVDNAGSVFVGAYTPESCGDYSSGTNH 728 ++ + +E+SNQY PEHLI+Q NA + V + +AGSVF+G ++PES GDY+SGTNH Sbjct: 308 IVTKDLAQCVEISNQYGPEHLIIQTRNARELVDSITSAGSVFLGDWSPESAGDYASGTNH 367 Query: 729 TLPTYGYARQYSGANTATFQKFITAQNITPEGLENIGRAVMCVAKKEGLDGHRNAVKIRM 788 LPTYGY S A FQK +T Q ++ EG + + +A E L H+NAV +R+ Sbjct: 368 VLPTYGYTATCSSLGLADFQKRMTVQELSKEGFSALASTIETLAAAERLTAHKNAVTLRV 427 Query: 789 SKL 791 + L Sbjct: 428 NAL 430 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: 714 Number of extensions: 36 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: 434 Length adjustment: 37 Effective length of query: 762 Effective length of database: 397 Effective search space: 302514 Effective search space used: 302514 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