Align aspartate kinase; homoserine dehydrogenase (EC 2.7.2.4; EC 1.1.1.3) (characterized)
to candidate BWI76_RS01790 BWI76_RS01790 lysine-sensitive aspartokinase 3
Query= reanno::Pedo557:CA265_RS23475 (817 letters) >FitnessBrowser__Koxy:BWI76_RS01790 Length = 449 Score = 215 bits (547), Expect = 5e-60 Identities = 149/462 (32%), Positives = 243/462 (52%), Gaps = 25/462 (5%) Query: 3 VLKFGGTSVGSAENIKTLLRLVGEEKQKNSPVVVLSAMSGVTNLLTEMAEMAERGEDYDT 62 V KFGGTSV + + + + + N+ VVVLSA +GVTNLL +AE E GE + Sbjct: 6 VAKFGGTSVADFDAMNRSVDVALLDA--NTRVVVLSASAGVTNLLVALAEGLEPGERF-A 62 Query: 63 HLKEIEAKHFAVIRSLLPAAAQNPVFTRLKIFFNELEDLLQAVANLREL-----SLQTKD 117 L + F ++ L + P R +E+E LL+ + L E S D Sbjct: 63 KLDAMRQIQFNILERL-----RYPNVIR-----DEIERLLENITTLAEAASLASSTALTD 112 Query: 118 QILSYGERCSTFMISHIASKNIGDSIYVNGSDLIKTDSNFGQAKVE-TELTEMLINNFYQ 176 +++S+GE ST + I + + + + +++T+ FG+A+ + L+E+ Sbjct: 113 ELVSHGELMSTLLFVEILRERGIAAQWFDVRKIMRTNDRFGRAEPDIAALSELTQQQLTP 172 Query: 177 ENKDKVLFVTGFIASNAAGRVTTLGRGGSDYTAAVWGAALNAEEIEIWTDVNGMMTADPR 236 + ++ GFI S A GR TTLGRGGSDYTAA+ G ALNA ++IWTDV G+ T DPR Sbjct: 173 RLAEGLVITQGFIGSEAKGRTTTLGRGGSDYTAALLGEALNATRVDIWTDVPGIYTTDPR 232 Query: 237 MVKKAFSLPELSYTEAMELSYFGAKVIYPPTMIPAFMKKIPIVIKNTFEPDFAGTYIKSD 296 + A + +++ EA E++ FGAKV++P T++PA IP+ + ++ EP GT + + Sbjct: 233 VAPAAKRIDVIAFEEAAEMATFGAKVLHPATLLPAVRSDIPVFVGSSKEPKAGGTLVCKN 292 Query: 297 VKASSLPIKGISSIDHISIINLTGSGMVGKAGFSGRLFSLLSREQINVVLITQSSSEHSI 356 K L + ++ +++ L M+ GF +FS+L+R I+V LIT +SE S+ Sbjct: 293 TKNPPL-FRALALRRKQTLLTLHSLNMLHSRGFLAEVFSILARHSISVDLIT--TSEVSV 349 Query: 357 TFAVKPTDASQAISLIKKEFELELDAKKLELPEVENNLAVLAIVGENMKRTPGMSGRLFN 416 + T ++ A + + L + L EVE +LA++AI+G + + G+ +F Sbjct: 350 ALTMDTTGSTSAGDTLLTQ-GLLTELSSLCRVEVEQDLALVAIIGNELSKACGVGKEVFG 408 Query: 417 ALGRNGINVRAIAQGSSEYNISVIISKDDLSKAVNAVHDAFF 458 L + N+R I G+S +N+ ++ D K V +H F Sbjct: 409 VL--DPFNIRMICYGASSHNLCFLVPGADAEKVVQKLHHNLF 448 Lambda K H 0.316 0.133 0.369 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: 669 Number of extensions: 34 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: 817 Length of database: 449 Length adjustment: 37 Effective length of query: 780 Effective length of database: 412 Effective search space: 321360 Effective search space used: 321360 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: 41 (21.6 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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:
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