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_092995230.1 BLP65_RS08235 PLP-dependent aspartate aminotransferase family protein
Query= SwissProt::P06106 (444 letters) >NCBI__GCF_900102855.1:WP_092995230.1 Length = 394 Score = 192 bits (488), Expect = 2e-53 Identities = 140/434 (32%), Positives = 209/434 (48%), Gaps = 52/434 (11%) Query: 2 PSHFDTVQLHAGQENPGDNAHRSRAVPIYATTSYVFENSKHGSQLFGLEVPGYVYSRFQ- 60 P H T +HAG+ D+A S P+Y TT++ F +++ + G +Y+R+ Sbjct: 6 PMHLATRCVHAGEL---DDAQGSPHTPLYTTTTFKFASTEAILDVVEGRAAGSLYTRYGL 62 Query: 61 NPTSNVLEERIAALEGGAAALAVSSGQAAQTLAIQGLAHTGDNIVSTSYLYGGTYNQFKI 120 NPT LE ++A+LEG AA A SG AA+T LA+ + +V YGGT Sbjct: 63 NPTIQSLEAKLASLEGAEAAFAFCSGMAAETALF--LAYGREGVVCIGDAYGGTLELLAD 120 Query: 121 SFKRFGIEARFVEGDNPEEFEKVFDERTKAVYLETIGNPKYNVPDFEKIVAIAHKHGIPV 180 FGI+ + G + E + + V+LET NP V D I AH HG + Sbjct: 121 QLPLFGIDTHLILGSELDRLEDLLAGGARLVFLETPTNPALEVFDLAAIAEKAHAHGALL 180 Query: 181 VVDNTFGAGGYFCQPIKYGADIVTHSATKWIGGHGTTIGGIIVDSGKFPWKDYPEKFPQF 240 VDNTF A QP+ GAD HSATK++GGH G ++ S + Sbjct: 181 AVDNTF-ASPVNQQPLALGADFAVHSATKYLGGHSDLTAGALMGS------------QEL 227 Query: 241 SQPAEGYHGTIYNEAYGNLAYIVHVRTELLRDLGPLMNPFASFLLLQGVETLSLRAERHG 300 P G+ ++LG + P LL + + TL +R + Sbjct: 228 LAPIFGWR----------------------KNLGSMPAPETCNLLARSLRTLVVRVRQQN 265 Query: 301 ENALKLAKWLEQSPYVSWVSYPGLASHSHHENAKKYLSNGFGGVLSFGVKDLPNADKETD 360 +A +A+ +++ P V V YPGL H+ A K +S GFGG+L+ V +AD E Sbjct: 266 ASAQAVAEAMQRHPRVRRVLYPGLPDFPGHDLAAKQMS-GFGGMLTIEV----DADTE-- 318 Query: 361 PFKLSGAQVVDNLKLASNLANVGDAKTLVIAPYFTTHKQLNDKEKLASGVTKDLIRVSVG 420 A VVD LKL + ++G A++LV P TTH L++ E+ G+ ++R+SVG Sbjct: 319 ----GTAAVVDRLKLFAIAPSLGGAESLVTQPVTTTHHGLSETERERRGINGAMVRLSVG 374 Query: 421 IEFIDDIIADFQQS 434 +E +D+IAD +Q+ Sbjct: 375 LEDAEDLIADLEQA 388 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: 400 Number of extensions: 16 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 444 Length of database: 394 Length adjustment: 32 Effective length of query: 412 Effective length of database: 362 Effective search space: 149144 Effective search space used: 149144 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: 50 (23.9 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