Align D-mannonate oxidoreductase; EC 1.1.1.57; Fructuronate reductase (uncharacterized)
to candidate WP_069333383.1 C8J29_RS07100 mannitol dehydrogenase family protein
Query= curated2:P39160 (486 letters) >NCBI__GCF_003046325.1:WP_069333383.1 Length = 477 Score = 289 bits (739), Expect = 2e-82 Identities = 180/480 (37%), Positives = 256/480 (53%), Gaps = 12/480 (2%) Query: 11 VARPSWDHSRLESRIVHLGCGAFHRAHQALYTHHLLESTDS-DWGICEVNLMPGNDRVLI 69 V RP++D L IVH+G G FHRAHQA+Y L + DW I + P + R+ Sbjct: 5 VTRPAYDRKALTPGIVHIGVGNFHRAHQAVYLDDLFALGEGHDWAILGAGVRPTDARMR- 63 Query: 70 ENLKKQQLLYTVAEKGAESTELKIIGSMKEALHPEIDGCEGILNAMARPQTAIVSLTVTE 129 E L Q L TV E + +G+M L E D ++ AM+ P+ IVSLTVTE Sbjct: 64 EALAAQDNLSTVIELDPAGHRARQVGAMVGFLPVEADNA-ALIEAMSDPRIRIVSLTVTE 122 Query: 130 KGYCADAASGQLDLNNPLIKHDLENPTAPKSAIGYIVEALRLRREKGLKAFTVMSCDNVR 189 GY DA SG D +P I D P P +A G I+ ALR RR+ G+ FTVMSCDN+ Sbjct: 123 GGYYVDA-SGAFDPTHPDIVADAAQPARPATAFGAILAALRARRDAGIAPFTVMSCDNLP 181 Query: 190 ENGHVAKVAVLGLAQARDPQLAAWIEENVTFPCTMVDRIVPAATPETLQEIADQLGVYDP 249 NGHV + AV+GLA+ D +LA W++ V FP MVDRI PA P +E+A G+ DP Sbjct: 182 GNGHVTRNAVVGLAELYDAELAGWVKAQVAFPNGMVDRITPATGPHE-RELAQGFGLADP 240 Query: 250 CAIACEPFRQWVIEDNFVNGRPDWDKVGAQFVADVVPFEMMKLRMLNGSHSFLAYLGYLG 309 + CEPFRQWVIED+F GRP +KVG F V +E MK+R+LNG H+ +AY L Sbjct: 241 VPVTCEPFRQWVIEDHFPAGRPALEKVGVTFTPHVHAYEAMKIRILNGGHAVIAYPSALM 300 Query: 310 GYETIADTVTNPAYRKAAFALMMQEQAPTLSMPEGTDLNAYATLLIERFSNPSLRHRTWQ 369 + + + + +P + ++E P ++ T + Y TL+ RFSNP + T + Sbjct: 301 DIQLVHEAMAHPLIAAFLHKVEVEEILPHVAPVPDTSIPDYLTLIESRFSNPEIADTTRR 360 Query: 370 IAMDGSQKLPQRLLDPVRLHLQNGGSWRHLALGVAGWMRYTQGVDEQGNAIDVVDPMLAE 429 + +DGS + P+ ++ +R +L G + L L A W RY G + G ++ DP Sbjct: 361 LCLDGSNRQPKFIVPSLRDNLAAGTVPKGLVLLSALWCRYCYGTTDSGVVVEPNDPNWTA 420 Query: 430 FQKINAQYQGADRVKALLGLSGIFADDLPQN----ADFVGAVTAAYQQLCERGARECVAA 485 Q + + + L ++ ++ DL QN A+F A+ A ++ E R +AA Sbjct: 421 LQ--DRARRAKETPAEWLAMTEVYG-DLAQNDLLAAEFAAALEAVWRDGAEAVLRRFLAA 477 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: 614 Number of extensions: 23 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: 477 Length adjustment: 34 Effective length of query: 452 Effective length of database: 443 Effective search space: 200236 Effective search space used: 200236 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