Align Threonine dehydratase 2 biosynthetic, chloroplastic; SlTD2; Threonine deaminase 2; EC 4.3.1.17; EC 4.3.1.19 (characterized)
to candidate WP_044051092.1 RCA23_RS15620 threonine ammonia-lyase IlvA
Query= SwissProt::P25306 (595 letters) >NCBI__GCF_000738435.1:WP_044051092.1 Length = 411 Score = 201 bits (512), Expect = 4e-56 Identities = 135/393 (34%), Positives = 207/393 (52%), Gaps = 13/393 (3%) Query: 113 SPLELAEKLSDRLGVNFYIKREDKQRVFSFKLRGAYNMMSNLSREELDKGV-ITASAGNH 171 +PL+ + LS+ + ++KRED V S+KLRGA+N M ++ DK V + ASAGNH Sbjct: 22 TPLQRNDHLSNVYDADIWLKREDLSPVRSYKLRGAFNAMG----KQADKDVFVCASAGNH 77 Query: 172 AQGVALAGQRLNCVAKIVMPTTTPQIKIDAVRALGG---DVVLYGKTFDEAQTHALELSE 228 AQGVA + L I MP TTP+ KI R GG V L G FD+ + Sbjct: 78 AQGVAYVCRHLQKKGVIFMPVTTPEQKIRKTRLFGGAWVQVQLVGDYFDDTLRASQAYCA 137 Query: 229 KDGLKYIPPFDDPGVIKGQGTIGTEINRQLKDIHAVFI-PVGGGGLIAGVATFFKQIAPN 287 + G ++ PFDDP VI+GQ T+ E+ QL VF+ PVGGGGL + + AP Sbjct: 138 EVGGHFLSPFDDPDVIEGQATVTYEMLEQLGRSPDVFVVPVGGGGLSSSARRLLSERAPE 197 Query: 288 TKIIGVEPYGAASMTLSLHEGHRVKLSNVDTFADGVAVALVGEYTFAKCQEL-IDGMVLV 346 T+I VEP G S+ ++ G + L VDTF DG AVA +G TFA + + D ++ + Sbjct: 198 TEIFYVEPSGGKSLAAAVQAGAPIALEQVDTFVDGAAVAKMGVNTFAALKGIDADHVLDI 257 Query: 347 ANDGISAAIKDVYDEGRNILETSGAVAIAGAAAYCEFYKIKNENIVAIASGANMDFSKLH 406 D I I D+ + +LE +GA+A+ + KIK + +V ++SG N DF +L Sbjct: 258 PEDRICTTILDMLNTEGIVLEPAGALALDALKDLKD--KIKGKTVVCVSSGGNFDFERLP 315 Query: 407 KVTELAGLGSGKEALLATFMVEQQGSFKTFVGLVG-SLNFTELTYRFTSERKNALILYRV 465 +V E A +G + + ++ G+ K F+GL+G + Y S R +L + Sbjct: 316 EVKERAQRYAGVKKYFILRLPQRPGALKDFLGLLGPDDDIARFEYLKKSARNFGTVLLGI 375 Query: 466 NVDKESDLEKMIEDMKSSNMTTLNLSHNELVVD 498 K + + E ++++ M+ +++ +E +VD Sbjct: 376 ETSKPENFALLSERLEAAGMSIRDITGDEAMVD 408 Lambda K H 0.317 0.135 0.382 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: 550 Number of extensions: 31 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: 595 Length of database: 411 Length adjustment: 34 Effective length of query: 561 Effective length of database: 377 Effective search space: 211497 Effective search space used: 211497 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 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 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:
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