Align D-mannonate oxidoreductase (EC 1.1.1.57) (characterized)
to candidate WP_087506848.1 CBE68_RS14645 fructuronate reductase
Query= ecocyc::MANNONOXIDOREDUCT-MONOMER (486 letters) >NCBI__GCF_002165625.1:WP_087506848.1 Length = 492 Score = 469 bits (1208), Expect = e-137 Identities = 243/488 (49%), Positives = 325/488 (66%), Gaps = 9/488 (1%) Query: 1 MTTIVDSNLPVA----RPSWDHSRLESRIVHLGCGAFHRAHQALYTHHLLESTDSDWGIC 56 MTT + NL + S+D S+LE+ IVH+G GAFHR HQA+Y + +D WGIC Sbjct: 1 MTTTTEVNLESLGFNEKTSFDRSKLETNIVHIGFGAFHRGHQAVYNDLTNDQSDKLWGIC 60 Query: 57 EVNLMPGNDRVLIENLKKQQLLYTVAEKGAESTELKIIGSMKEALHPEIDGCEGILNAMA 116 E+N+ G + LI +L+ QQ L++V E+ A+S ++I S+ E++H +DG + ++ +A Sbjct: 61 EINMFGGPE--LIADLQAQQHLFSVVERSADSMVSRLIRSVTESIHTPVDGIQAAIDKLA 118 Query: 117 RPQTAIVSLTVTEKGYCADAASGQLDLNNPLIKHDLENPTAPKSAIGYIVEALRLRREKG 176 PQ IVSLT+TEKGYC+D SGQLD+NN LI+HDL NP P+SA+G I EALR+RR+KG Sbjct: 119 EPQVKIVSLTITEKGYCSDPQSGQLDINNGLIQHDLNNPQTPQSALGLITEALRVRRDKG 178 Query: 177 LKAFTVMSCDNVRENGHVAKVAVLGLAQARDPQLAAWIEENVTFPCTMVDRIVPAATPET 236 L F+V+SCDN+ ENG + K AVL A+ D LAAWIE+NVTFP TMVDRIVPA T + Sbjct: 179 LAPFSVLSCDNIPENGLLTKEAVLSFAKQLDSALAAWIEQNVTFPSTMVDRIVPAMTDDA 238 Query: 237 LQEIADQLGVYDPCAIACEPFRQWVIEDNFVNGRPDWDKVGAQFVADVVPFEMMKLRMLN 296 I + +G DPC I CE +RQWVIEDNFV GRPDWDK GA FVADV+P+E MKLRMLN Sbjct: 239 FAVIDECIGYRDPCGIVCEDYRQWVIEDNFVAGRPDWDKAGAMFVADVLPYEEMKLRMLN 298 Query: 297 GSHSFLAYLGYLGGYETIADTVTNPAYRKAAFALMMQEQAPTLSMPEGTDLNAYATLLIE 356 GSHSFLAY G+L GY+ I + + +R LM++EQA +L+ DL YA+LLI Sbjct: 299 GSHSFLAYNGFLAGYDFIYQCMEDSDFRATTLRLMLEEQAKSLNPSLKVDLEQYASLLIG 358 Query: 357 RFSNPSLRHRTWQIAMDGSQKLPQRLLDPVRLHLQNGGSWRHLALGVAGWMRYTQGVDEQ 416 RFSNP+++H+T QIAMDG+QKLPQR +DP+ L+ G + L +AGW + ++ Sbjct: 359 RFSNPNIKHKTAQIAMDGTQKLPQRAIDPMLTLLERGITPTCQPLLIAGWATFV--INAV 416 Query: 417 GNAIDVVDPMLAEF-QKINAQYQGADRVKALLGLSGIFADDLPQNADFVGAVTAAYQQLC 475 N D+VDPM + Q +N+ ++++ALL L IF N F + AA+ L Sbjct: 417 SNGDDLVDPMAEQLKQAVNSATTAEEQLEALLALEQIFGQHPQSNETFAALIKAAFVNLQ 476 Query: 476 ERGARECV 483 E G + V Sbjct: 477 ETGIKGLV 484 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: 665 Number of extensions: 30 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: 492 Length adjustment: 34 Effective length of query: 452 Effective length of database: 458 Effective search space: 207016 Effective search space used: 207016 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