Align D-mannonate oxidoreductase (EC 1.1.1.57) (characterized)
to candidate WP_156172064.1 AAW01_RS05295 mannitol dehydrogenase family protein
Query= ecocyc::MANNONOXIDOREDUCT-MONOMER (486 letters) >NCBI__GCF_001010925.1:WP_156172064.1 Length = 486 Score = 338 bits (867), Expect = 2e-97 Identities = 194/480 (40%), Positives = 283/480 (58%), Gaps = 12/480 (2%) Query: 10 PVAR-PSWDHSRLESRIVHLGCGAFHRAHQALYTHHLLESTDSDWGICEVNLMPGNDRVL 68 P AR P +D ++ ++HLG GAFHRAHQA Y LL + + W IC +L + Sbjct: 4 PEARTPCYDRAQ-PCGVLHLGTGAFHRAHQATYFDALLSAGHNGWMICGASL---RSPAV 59 Query: 69 IENLKKQQLLYTVAEKGAESTELKIIGSMKEALHPEIDGCEGILNAMARPQTAIVSLTVT 128 + Q L+TV + +++I+GS+ E + + +++A+A A+V+LTVT Sbjct: 60 SRQMNPQDGLFTVLIRDGGEEQVEIVGSVAEVMVAP-ENPSALVSALAHSDVALVTLTVT 118 Query: 129 EKGYCADAASGQLDLNNPLIKHDLENPTAPKSAIGYIVEALRLRREKGLKAFTVMSCDNV 188 EKGYC D A+G L+L++ + D+ + +P++A G++V L R+ G+ FTV+SCDN+ Sbjct: 119 EKGYCLDPATGALNLDDEGVAGDIADIASPQTAPGFLVAGLAARKAAGIAPFTVLSCDNL 178 Query: 189 RENGHVAKVAVLGLAQARDPQLAAWIEENVTFPCTMVDRIVPAATPETLQEIADQLGVYD 248 +NG + AVL LA+A DP LA WIE+ V FPC+MVDRIVPA T E L G+ D Sbjct: 179 PDNGKRTREAVLTLARAVDPALATWIEDEVAFPCSMVDRIVPATTEEDLDNFESATGLRD 238 Query: 249 PCAIACEPFRQWVIEDNFVNGRPDWDKVGAQFVADVVPFEMMKLRMLNGSHSFLAYLGYL 308 + EPF QWV+ED+F N RP D+VG Q DV +E++KLR+LNG+HS LAYLG L Sbjct: 239 EALVKTEPFTQWVVEDDFCNRRPPLDEVGVQMTNDVASWELVKLRLLNGAHSALAYLGGL 298 Query: 309 GGYETIADTVTNPAYRKAAFALMMQEQAPTLSMPEGTDLNAYATLLIERFSNPSLRHRTW 368 G+ + + P + + AL + +A TL +G D Y L +RF+N +L HRT Sbjct: 299 AGHHYVHQAMAAPGFSRLVEALWDEAEA-TLKPIDGFDAKNYRAQLAQRFTNSALEHRTH 357 Query: 369 QIAMDGSQKLPQRLLDPVRLHLQ-NGGSWRHLALGVAGWMRYTQGVDEQGNAIDVVDPML 427 QIAMDGSQK+PQR L+ +R + + + G + L + +AGWM + G ++ G V DP+ Sbjct: 358 QIAMDGSQKIPQRWLNTIRAYREADRGVPKALVMALAGWMHWQAGKNDAGETHIVDDPLA 417 Query: 428 AEFQKINAQYQGADRVKA---LLGLSGIFADDLPQNADFVGAVTAAYQQLCERGARECVA 484 A + G DR++ LLG+S IF + LP + FV +T AY + E A + VA Sbjct: 418 ARTAAALREAAG-DRMREVANLLGISAIFGEALPADNAFVQHLTEAYCSIGETSAADAVA 476 Lambda K H 0.320 0.135 0.408 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: 626 Number of extensions: 24 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: 486 Length of database: 486 Length adjustment: 34 Effective length of query: 452 Effective length of database: 452 Effective search space: 204304 Effective search space used: 204304 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. 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