Align O-acetyl-L-homoserine sulfhydrylase; OAH sulfhydrylase; O-acetylhomoserine thiolase; EC 2.5.1.- (characterized)
to candidate WP_013841856.1 DESRU_RS09300 homocysteine synthase
Query= SwissProt::Q9WZY4 (430 letters) >NCBI__GCF_000215085.1:WP_013841856.1 Length = 427 Score = 537 bits (1384), Expect = e-157 Identities = 269/427 (62%), Positives = 340/427 (79%), Gaps = 4/427 (0%) Query: 1 MDWKKYGYNTRALHAGYEPPEQATGSRAVPIYQTTSYVFRDSDHAARLFALEEPGFIYTR 60 M +K G+ T ALHAG++P ++ T SRAVPIYQT+SYVFRDS+HAA LF+L+E G IYTR Sbjct: 1 MTERKLGFETLALHAGHQP-DRETLSRAVPIYQTSSYVFRDSEHAANLFSLKEEGHIYTR 59 Query: 61 IGNPTVSVLEERIAALEEGVGALAVASGQAAITYAILNIAGPGDEIVSGSALYGGTYNLF 120 I NPT VLE+R+AALE GVGALA+ASG AAI AILNIA GDEIVS + LYGGT NLF Sbjct: 60 IDNPTTDVLEKRLAALEGGVGALAMASGHAAIVAAILNIASAGDEIVSSTNLYGGTVNLF 119 Query: 121 RHTLYKKSGIIVKFVDETDPKNIEEAITEKTKAVYLETIGNPGLTVPDFEAIAEIAHRHG 180 HT + + GI V FV+ DP+N +AITEKTKA++ ETIGNP V D EA+ +IAH+ Sbjct: 120 THT-FARLGIKVVFVNPEDPENFRKAITEKTKALFAETIGNPRCDVLDLEAVGKIAHQAE 178 Query: 181 VPLIVDNT-VAPYIFRPFEHGADIVVYSATKFIGGHGTSIGGLIVDSGKFDWT-NGKFPE 238 +PLIVD+T PY+ RPF++GADIVV+S TKFIGGHGTSIGG+I+DSGKFDW+ N KFP Sbjct: 179 IPLIVDSTFTTPYLCRPFDYGADIVVHSTTKFIGGHGTSIGGVIIDSGKFDWSQNDKFPG 238 Query: 239 LVEPDPSYHGVSYVETFKEAAYIAKCRTQLLRDLGSCMSPFNAFLFILGLETLSLRMKKH 298 L +PDPSYH ++Y + AAYIAK RTQLLRDLG+C+SPFNAFL + G+ETL+LRM++H Sbjct: 239 LNQPDPSYHDITYTKEMGAAAYIAKARTQLLRDLGACVSPFNAFLLLQGIETLALRMERH 298 Query: 299 CENALKIVEFLKSHPAVSWVNYPIAEGNKTRENALKYLKEGYGAIVTFGVKGGKEAGKKF 358 NA ++ EFL+ H V+WV+YP +G+ + E A KYL +G GAI+TFG+KGG EAG++F Sbjct: 299 VSNAQRVAEFLQQHSLVNWVSYPGIKGHPSYELAQKYLPKGAGAILTFGIKGGLEAGRRF 358 Query: 359 IDSLTLISHLANIGDARTLAIHPASTTHQQLTEEEQLKTGVTPDMIRLSVGIEDVEDIIA 418 IDSL + SHLAN+GDA++L IHPASTTH QL+EE + GV+PD+IR+SVG+E + D++ Sbjct: 359 IDSLQIFSHLANVGDAKSLVIHPASTTHSQLSEEALKQAGVSPDLIRISVGLESIGDLLE 418 Query: 419 DLDQALR 425 DLDQAL+ Sbjct: 419 DLDQALK 425 Lambda K H 0.317 0.136 0.398 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: 585 Number of extensions: 21 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: 430 Length of database: 427 Length adjustment: 32 Effective length of query: 398 Effective length of database: 395 Effective search space: 157210 Effective search space used: 157210 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