Align D-mannonate oxidoreductase; EC 1.1.1.57; Fructuronate reductase (uncharacterized)
to candidate WP_079649361.1 B5X82_RS16985 mannitol dehydrogenase family protein
Query= curated2:P39160 (486 letters) >NCBI__GCF_900167915.1:WP_079649361.1 Length = 484 Score = 259 bits (661), Expect = 2e-73 Identities = 181/481 (37%), Positives = 247/481 (51%), Gaps = 25/481 (5%) Query: 6 DSNLP--VARPSWDHSRLESRIVHLGCGAFHRAHQALYTHHLLESTDSDWGICEVNLMPG 63 D+ +P VA + R S IVHLG GAFHRAHQA+YT + D+ WGI V+L Sbjct: 13 DATMPEGVAPLRYVRDRARSGIVHLGLGAFHRAHQAVYTDDAMAVGDAGWGIVGVSLRSP 72 Query: 64 NDRVLIENLKKQQLLYTVAEKGAESTELKIIGSMKEAL-HPEIDGCEGILNAMARPQTAI 122 R + L Q LY V E+GA +++GS+ +AL PE E ++ A+A P + Sbjct: 73 AVR---DALVPQDCLYIVEERGAPGGR-RLVGSINDALVAPEAP--ERVIAALADPAVHV 126 Query: 123 VSLTVTEKGYCADAASGQLDLNNPLIKHDLENPTAPKSAIGYIVEALRLRREKGLKAFTV 182 +LTVTEKGY D + L ++ P + HDL P++ G++ AL R +G T+ Sbjct: 127 ATLTVTEKGYHRDPRTNGLLVDAPDVAHDLGGGD-PRTIFGFLAAALDRRAARGAGPLTI 185 Query: 183 MSCDNVRENGHVAKVAVLGLAQARD-PQLAAWIEENVTFPCTMVDRIVPAATPETLQEIA 241 +SCDN+ +NG + + AR + W T P MVDRIVPA T + Sbjct: 186 LSCDNLPDNGRLLGGLLDDYLAARGGARPGGW-----TSPSGMVDRIVPAITADDFA--- 237 Query: 242 DQLGVYDPCAIACEPFRQWVIEDNFVNGRPDWDKVGAQFVADVVPFEMMKLRMLNGSHSF 301 +L V D CEPFRQWVIED F RP W+ GAQ V DV PFE+ KLR+LNG+HS Sbjct: 238 -RLPVEDRALTVCEPFRQWVIEDRFAGPRPRWEAGGAQIVDDVRPFELAKLRLLNGAHSA 296 Query: 302 LAYLGYLGGYETIADTVTNPAYRKAAFALMMQEQAPTLSMPEGTDLNAYATLLIERFSNP 361 LAY G G+ + + V +P ++ E AP+L D AY ++ RF NP Sbjct: 297 LAYWGLPLGHAYVHEAVRDPDLLAFVRRQLLAEAAPSLPPSAALDPAAYVEAILRRFDNP 356 Query: 362 SLRHRTWQIAMDGSQKLPQRLLDPVRLHLQNG-GSWRHLALGVAGWMRYTQGVDEQGNAI 420 +L HR QIAMDGSQKLPQR L + G S HL VA W+ + G Sbjct: 357 ALPHRLAQIAMDGSQKLPQRWLATLVERAATGLASPAHLR-SVAAWLAFVGDASGGGRPA 415 Query: 421 DVVDPMLAEFQKI-NAQYQGADRVKALLGLSGIFADDLPQNADFVGAVTAAYQQLCERGA 479 D DP+ + + I + Q A+ A++ SG+F + V A+ A + +G Sbjct: 416 D--DPLASRLETIWDGQATPAEIATAIVRSSGVFPAAFGADEALVRALGEALAERLSKGP 473 Query: 480 R 480 R Sbjct: 474 R 474 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: 700 Number of extensions: 43 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: 486 Length of database: 484 Length adjustment: 34 Effective length of query: 452 Effective length of database: 450 Effective search space: 203400 Effective search space used: 203400 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