Align 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione acylhydrolase (ring-opening) (EC 3.7.1.22) (characterized)
to candidate WP_012631041.1 MNOD_RS38625 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione acylhydrolase (decyclizing)
Query= BRENDA::Q9L3I0 (626 letters) >NCBI__GCF_000022085.1:WP_012631041.1 Length = 612 Score = 699 bits (1803), Expect = 0.0 Identities = 366/618 (59%), Positives = 439/618 (71%), Gaps = 13/618 (2%) Query: 11 MGKTIRLTMAQAVAHFLKVQMTIVDGKKVPIFGGVWAIFGHGNVAGIGEALYQVREELTT 70 M T+RLT AQ + +L VQMT +G++ GVWAIFGHGNVAGIGEAL ++ + L T Sbjct: 1 MMTTVRLTAAQTMMRWLSVQMT-EEGER--FIEGVWAIFGHGNVAGIGEALEKIGDALPT 57 Query: 71 YRAHNEQGMAHAAIAYAKANFRTRFMACTSSIGPGALNMVTAAGVAHVNRIPVLFLPGDV 130 +R NEQ MAHAAIAYAK R + MA TSSIGPGA NMVTAA +AHVNR+PVL +PGDV Sbjct: 58 WRGQNEQTMAHAAIAYAKTKRRRKAMAVTSSIGPGATNMVTAAALAHVNRLPVLLIPGDV 117 Query: 131 FANRAPDPVLQQIEDSATASVSANDAFRSVSRYFDRITRPEQIITALKRAMQVLTDPLDC 190 FANR PDPVLQQIED +VSAND FR VSRYFDRITRPE ++TAL RA+QV+TDP C Sbjct: 118 FANRRPDPVLQQIEDFDDGTVSANDCFRPVSRYFDRITRPEHLLTALPRALQVMTDPAQC 177 Query: 191 GPVTLSLCQDVQAEAYDYPESLFAEKVWTTRRPQPDADELANAIALIKASQKPVIVAGGG 250 GPVTL+ CQDVQAEAYD+PE+ FA KVW RRP+PD ELA I +I+A+QKPVIV+GGG Sbjct: 178 GPVTLAFCQDVQAEAYDWPEAFFAPKVWHIRRPEPDRRELAAVIEMIRAAQKPVIVSGGG 237 Query: 251 VLYSQATKELAAFAEAHGIPVVVSQAGKSAINETHPLALGSVGVTGTSAANAIAEETDLV 310 VLYS A ++LAAFAE H IPVV +QAGK A++ HPL GS GVTG+ AN I E DL+ Sbjct: 238 VLYSGADQDLAAFAEKHNIPVVETQAGKGALDWQHPLNFGSPGVTGSDCANRICAEADLI 297 Query: 311 IAVGTRCQDFTTGSWALFKNDSLKMIGLNIAAYDAVKHDSHPLVADAREGLKALSAGLSG 370 I GTR QDFTTGSWA F+N K++ +N+ YDA KH + PLVADA+ L A++AGL G Sbjct: 298 IGAGTRFQDFTTGSWAAFRNPQRKLVSVNLTGYDAAKHSAVPLVADAKIALTAITAGLEG 357 Query: 371 WKAPAALAEKAAAEKKIWMEAAARAMATTNAA----LPSDAQVIGAVARTIGGENTTVLC 426 + A A+ + W +AA R MA LP+DAQV+GAV R G +T V+C Sbjct: 358 HR----FAGPDASLRTAWFKAADRVMAAPQGENPNDLPTDAQVVGAVQR-YAGADTVVMC 412 Query: 427 AAGGLPGELHKLWPATAPGSYHMEYGFSCMGYEIAGGLGAKMARPERDVVVMVGDGSYMM 486 AAG +PG L LW A APG YHMEYG+SCMGYE+AG +G +A PE++V+ VGDGSYMM Sbjct: 413 AAGTMPGALQVLWRA-APGGYHMEYGYSCMGYEVAGAMGIALAVPEKEVICFVGDGSYMM 471 Query: 487 MNSELATSVMLGLKLNIIVLDNRGYGCINRLQMGTGGANFNNLLKDSYHEVMPEIDFRAH 546 NSELAT+ M+ + I++ DNRGYGCINRLQ+ GGA FNN+ DS H+ PEIDF AH Sbjct: 472 ANSELATAAMMHVPFTIVLTDNRGYGCINRLQIECGGAPFNNMYVDSRHKTFPEIDFVAH 531 Query: 547 AESMGAIAVKVASIAELEQALADSRKNDRTSVFVIDTDPLITTEAGGHWWDVAVPEVSSR 606 A +MGA AVKVA IA LE LA R V +IDT+ + GG WWDVAVPEV + Sbjct: 532 ARAMGAEAVKVAGIAGLEAELARPRDRKVPRVILIDTEAESSLGVGGAWWDVAVPEVGTT 591 Query: 607 SEVNRAHEAYVKARAAQR 624 + A E Y A QR Sbjct: 592 EALRAARERYDSHAAFQR 609 Lambda K H 0.318 0.131 0.382 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: 1020 Number of extensions: 37 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: 626 Length of database: 612 Length adjustment: 37 Effective length of query: 589 Effective length of database: 575 Effective search space: 338675 Effective search space used: 338675 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 (21.7 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
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