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_011735676.1 PPRO_RS08900 homocysteine synthase
Query= SwissProt::P06106 (444 letters) >NCBI__GCF_000015045.1:WP_011735676.1 Length = 428 Score = 455 bits (1171), Expect = e-132 Identities = 232/431 (53%), Positives = 305/431 (70%), Gaps = 15/431 (3%) Query: 6 DTVQLHAGQENPGDNAHRSRAVPIYATTSYVFENSKHGSQLFGLEVPGYVYSRFQNPTSN 65 +T+ LHAGQ D+ SRAVPIY T+SYVF NS+H + LFGL+ PG +Y+R NPT++ Sbjct: 9 ETLALHAGQSP--DSETLSRAVPIYQTSSYVFRNSEHAANLFGLKEPGNIYTRLMNPTTD 66 Query: 66 VLEERIAALEGGAAALAVSSGQAAQTLAIQGLAHTGDNIVSTSYLYGGTYNQFKISFKRF 125 VLE R+AAL+GG ALAV+SGQAA T A+ + G NIVSTS+LYGGTYN F + R Sbjct: 67 VLERRMAALDGGVGALAVASGQAAITYAVLNITSAGQNIVSTSFLYGGTYNLFHYTLPRL 126 Query: 126 GIEARFVEGDNPEEFEKVFDERTKAVYLETIGNPKYNVPDFEKIVAIAHKHGIPVVVDNT 185 GI+ +FV+ +PE + D+ T+ VY E++GNPK NV DFE I AIAH+ GIP+VVDNT Sbjct: 127 GIQVKFVDSSDPENIRRAIDQDTRLVYSESVGNPKNNVDDFEAIAAIAHEAGIPLVVDNT 186 Query: 186 FGAGGYFCQPIKYGADIVTHSATKWIGGHGTTIGGIIVDSGKFPWKDYPEKFPQFSQPAE 245 F +P+ +GADIV +S TK+I GHGT+IGG IVD G F W + +FP+ ++P Sbjct: 187 VTTPWLF-KPLDHGADIVVYSLTKFIAGHGTSIGGAIVDGGTFNWDN--GRFPELTEPDP 243 Query: 246 GYHGTIYNEAYGNLAYIVHVRTELLRDLGPLMNPFASFLLLQGVETLSLRAERHGENALK 305 YHG Y EA G+ AYI+ +R LLRD+G ++PF SF +LQG+ETL +R RH ENA Sbjct: 244 SYHGLKYWEALGSQAYILKMRVTLLRDMGACLSPFNSFQILQGLETLHVRMPRHVENARC 303 Query: 306 LAKWLEQSPYVSWVSYPGLASHSHHENAKKYLSNGFGGVLSFGVKDLPNADKETDPFKLS 365 +A WLE+ P VSWV+YPGLASH H NA+KYL G G ++ FG+K A Sbjct: 304 VASWLERHPLVSWVNYPGLASHRDHANARKYLPKGEGAIIGFGIKGGVKA---------- 353 Query: 366 GAQVVDNLKLASNLANVGDAKTLVIAPYFTTHKQLNDKEKLASGVTKDLIRVSVGIEFID 425 G++ +DN+KL S+LAN+GDAK+LVI P TTH+QL+++E+LASGV+ D IR+S+G+E ID Sbjct: 354 GSKFIDNVKLLSHLANIGDAKSLVIHPASTTHQQLSEEEQLASGVSPDFIRLSIGLENID 413 Query: 426 DIIADFQQSFE 436 DIIAD Q+ E Sbjct: 414 DIIADISQALE 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: 531 Number of extensions: 21 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: 444 Length of database: 428 Length adjustment: 32 Effective length of query: 412 Effective length of database: 396 Effective search space: 163152 Effective search space used: 163152 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