Align Homocysteine/cysteine synthase; O-acetylserine/O-acetylhomoserine sulfhydrylase; OAS-OAH SHLase; OAS-OAH sulfhydrylase; EC 2.5.1.47; EC 2.5.1.49 (characterized)
to candidate WP_011840796.1 RSPH17029_RS05580 O-acetylhomoserine aminocarboxypropyltransferase/cysteine synthase
Query= SwissProt::P06106 (444 letters) >NCBI__GCF_000015985.1:WP_011840796.1 Length = 430 Score = 376 bits (965), Expect = e-109 Identities = 201/430 (46%), Positives = 276/430 (64%), Gaps = 14/430 (3%) Query: 5 FDTVQLHAGQENPGDNAHRSRAVPIYATTSYVFENSKHGSQLFGLEVPGYVYSRFQNPTS 64 FDT+Q+HAG + D A +R VPIY TT+YVF +++H ++LF LE GY+YSR NPT Sbjct: 9 FDTLQIHAGAKP--DPATGARQVPIYQTTAYVFRDAEHAARLFNLEEVGYIYSRLTNPTV 66 Query: 65 NVLEERIAALEGGAAALAVSSGQAAQTLAIQGLAHTGDNIVSTSYLYGGTYNQFKISFKR 124 L ER+AALEGGA A+ SSG AAQ +A+ L G NIV+++ LYGGT QF + +R Sbjct: 67 MALAERVAALEGGAGAVCCSSGHAAQIMALFPLMAPGRNIVASTRLYGGTITQFSQTIRR 126 Query: 125 FGIEARFVEGDNPEEFEKVFDERTKAVYLETIGNPKYNVPDFEKIVAIAHKHGIPVVVDN 184 FG A+FV+ D+P E D T+A++ ETI NP + D + + AIA K G+P++VDN Sbjct: 127 FGWSAKFVDFDDPAAIEAAIDSDTRALFCETIANPGGVITDLDAVSAIADKMGLPLIVDN 186 Query: 185 TFGAGGYFCQPIKYGADIVTHSATKWIGGHGTTIGGIIVDSGKFPWKDYPEKFPQFSQPA 244 T A + C+PI++GA +V HSATK++ G+GT GG+IVDSGKF W +KFP SQP Sbjct: 187 T-TATPWLCRPIEHGATLVVHSATKYLTGNGTVTGGVIVDSGKFDW-SASDKFPSLSQPE 244 Query: 245 EGYHGTIYNEAYGNLAYIVHVRTELLRDLGPLMNPFASFLLLQGVETLSLRAERHGENAL 304 YHG ++++A G +AY H LRDLG MNP + L G+ETLSLR RH ENA Sbjct: 245 PAYHGLVFHKALGPMAYTFHSIAVGLRDLGMTMNPQGAHYTLMGIETLSLRMARHVENAQ 304 Query: 305 KLAKWLEQSPYVSWVSYPGLASHSHHENAKKYLSNGFGGVLSFGVKDLPNADKETDPFKL 364 K+A WLEQ P V +VSY GL S H + G G + +F VK +A Sbjct: 305 KVAAWLEQDPRVEFVSYAGLPSSPWHGRVARICPKGAGALFTFAVKGGYDA--------- 355 Query: 365 SGAQVVDNLKLASNLANVGDAKTLVIAPYFTTHKQLNDKEKLASGVTKDLIRVSVGIEFI 424 +VD L+L S++AN+GD ++LVI TTH+QL ++++A+G +++R+S+GIE Sbjct: 356 -CVALVDALQLFSHVANLGDTRSLVIHSASTTHRQLTPEQQVAAGAAPNVVRISIGIEDA 414 Query: 425 DDIIADFQQS 434 DD+IAD Q+ Sbjct: 415 DDLIADLDQA 424 Lambda K H 0.317 0.136 0.402 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: 484 Number of extensions: 24 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: 444 Length of database: 430 Length adjustment: 32 Effective length of query: 412 Effective length of database: 398 Effective search space: 163976 Effective search space used: 163976 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: 51 (24.3 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