Align D-mannonate oxidoreductase; EC 1.1.1.57; Fructuronate reductase (uncharacterized)
to candidate GFF1300 PGA1_c13160 mannitol 2-dehydrogenase MtlK
Query= curated2:P39160 (486 letters) >lcl|FitnessBrowser__Phaeo:GFF1300 PGA1_c13160 mannitol 2-dehydrogenase MtlK Length = 488 Score = 280 bits (716), Expect = 8e-80 Identities = 172/423 (40%), Positives = 234/423 (55%), Gaps = 8/423 (1%) Query: 7 SNLP--VARPSWDHSRLESRIVHLGCGAFHRAHQALYTHHLLES-TDSDWGICEVNLMPG 63 S LP + RPS+D + + IVH+G G FHRAHQA Y H L++S DWGI + Sbjct: 9 SQLPQTIGRPSYDRAEISPGIVHIGLGNFHRAHQAWYLHALMQSGLAMDWGIIGAGVRAA 68 Query: 64 NDRVLIENLKKQQLLYTVAEKGAESTELKIIGSMKEALHPEIDGCEGILNAMARPQTAIV 123 D + + L Q L T+ E ++IG + + L E D ++ MA IV Sbjct: 69 -DAGMRDRLLAQDCLTTLIELDPTGRSAEVIGPLIDFLPVEADNAS-LIRCMAGSPIRIV 126 Query: 124 SLTVTEKGYCADAASGQLDLNNPLIKHDLENPTAPKSAIGYIVEALRLRREKGLKAFTVM 183 SLTVTE GY DA LDLN+ I+HD+ P P++ G IVEALRLRR +GL AFTV Sbjct: 127 SLTVTEGGYYQDAQHKGLDLNHEDIRHDIARPDRPRTVFGAIVEALRLRRGRGLPAFTVQ 186 Query: 184 SCDNVRENGHVAKVAVLGLAQARDPQLAAWIEENVTFPCTMVDRIVPAATPETLQEIADQ 243 SCDN++ NG + + AV+ LAQ DP+LAAWI++ FP +MVD IVPA P + +A Sbjct: 187 SCDNLQGNGQITRTAVVTLAQQTDPELAAWIDQTGAFPNSMVDCIVPATGPAEI-ALARG 245 Query: 244 LGVYDPCAIACEPFRQWVIEDNFVNGRPDWDKVGAQFVADVVPFEMMKLRMLNGSHSFLA 303 G+ D + E +R WVIED F GRP WD GA F DV +E MK+R+LN H LA Sbjct: 246 YGIEDTAPVTHENYRHWVIEDEFCAGRPPWDLAGAIFTDDVHGYESMKIRVLNAGHQVLA 305 Query: 304 YLGYLGGYETIADTVTNPAYRKAAFALMMQEQAP-TLSMPEGTDLNAYATLLIERFSNPS 362 G L TIAD + +P + E P +++PE + Y TL+ RFSNP Sbjct: 306 NAGELLSIATIADCMKDPLLAAFFRTVQTAEILPHVIAVPEMAPKD-YLTLIEARFSNPE 364 Query: 363 LRHRTWQIAMDGSQKLPQRLLDPVRLHLQNGGSWRHLALGVAGWMRYTQGVDEQGNAIDV 422 +R T ++A DGS + P ++ +R +++ G+ L L A W + G+ E + I Sbjct: 365 IRDTTRRVAYDGSSRHPGFVMPILRDAVRSKGAIDGLCLVEALWAQMCTGLREDASEIAP 424 Query: 423 VDP 425 DP Sbjct: 425 NDP 427 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: 603 Number of extensions: 20 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: 488 Length adjustment: 34 Effective length of query: 452 Effective length of database: 454 Effective search space: 205208 Effective search space used: 205208 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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