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 PP_2528 PP_2528 O-acetylhomoserine (thiol)-lyase
Query= SwissProt::P06106 (444 letters) >FitnessBrowser__Putida:PP_2528 Length = 425 Score = 412 bits (1058), Expect = e-119 Identities = 210/431 (48%), Positives = 284/431 (65%), Gaps = 13/431 (3%) Query: 6 DTVQLHAGQENPGDNAHRSRAVPIYATTSYVFENSKHGSQLFGLEVPGYVYSRFQNPTSN 65 +T+ +HAG D ++ AVPIY TTS+ F++++HG+ LF L+V G +YSR NPT++ Sbjct: 4 ETLAIHAGFSP--DPTTKAVAVPIYQTTSFAFDDTQHGADLFDLKVAGNIYSRIMNPTND 61 Query: 66 VLEERIAALEGGAAALAVSSGQAAQTLAIQGLAHTGDNIVSTSYLYGGTYNQFKISFKRF 125 VLE+R+AALEGG ALAV+SG AA T AIQ +A GDNIVS + LYGGTYN + R Sbjct: 62 VLEQRMAALEGGVGALAVASGMAAITYAIQTVAEAGDNIVSVAKLYGGTYNLLAHTLPRM 121 Query: 126 GIEARFVEGDNPEEFEKVFDERTKAVYLETIGNPKYNVPDFEKIVAIAHKHGIPVVVDNT 185 GI RF D+ E + D RTKAV+ E+IGNP N+ D + AH+HG+P++VDNT Sbjct: 122 GIHTRFAAHDDIAALEALIDARTKAVFCESIGNPAGNIVDIAALAEAAHRHGVPLIVDNT 181 Query: 186 FGAGGYFCQPIKYGADIVTHSATKWIGGHGTTIGGIIVDSGKFPWKDYPEKFPQFSQPAE 245 A C+P ++GADIV HS TK+IGGHGT+IGGI++DSGKFPW + E+F + P Sbjct: 182 V-ATPVLCRPFEHGADIVVHSLTKYIGGHGTSIGGIVIDSGKFPWAENKERFALLNTPDP 240 Query: 246 GYHGTIYNEAYGNLAYIVHVRTELLRDLGPLMNPFASFLLLQGVETLSLRAERHGENALK 305 YHG Y EA+G A+I R LR+ G ++PF +FL+LQG+ETL+LR ERH ENALK Sbjct: 241 SYHGVTYTEAFGPAAFIGRCRVVPLRNTGAALSPFNAFLILQGLETLALRMERHTENALK 300 Query: 306 LAKWLEQSPYVSWVSYPGLASHSHHENAKKYLSNGFGGVLSFGVKDLPNADKETDPFKLS 365 +A +L+ V+WV + GL H H A++Y +LSFG+K + + Sbjct: 301 VAHYLQAHEQVAWVKFAGLPDHPEHALAQRYTGGKPASILSFGIKG----------GQAA 350 Query: 366 GAQVVDNLKLASNLANVGDAKTLVIAPYFTTHKQLNDKEKLASGVTKDLIRVSVGIEFID 425 GA+ +D L+L L N+GDAK+L P TTH+QLND E +GV +D++R+S+GIE D Sbjct: 351 GARFIDALQLVVRLVNIGDAKSLACHPASTTHRQLNDDELEKAGVPRDMVRLSIGIEHSD 410 Query: 426 DIIADFQQSFE 436 DIIAD Q+ E Sbjct: 411 DIIADLAQALE 421 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: 538 Number of extensions: 23 Number of successful extensions: 3 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: 425 Length adjustment: 32 Effective length of query: 412 Effective length of database: 393 Effective search space: 161916 Effective search space used: 161916 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