Align D-mannonate oxidoreductase (EC 1.1.1.57) (characterized)
to candidate WP_007675858.1 BN137_RS06955 fructuronate reductase
Query= ecocyc::MANNONOXIDOREDUCT-MONOMER (486 letters) >NCBI__GCF_000319285.1:WP_007675858.1 Length = 488 Score = 573 bits (1477), Expect = e-168 Identities = 291/488 (59%), Positives = 348/488 (71%), Gaps = 5/488 (1%) Query: 1 MTTIVDSNLP--VARPSWDHSRLESRIVHLGCGAFHRAHQALYTHHLLESTDSDWGICEV 58 M I + LP V RP +D L++RIVH G GAFHRAHQAL T +L DWGICE+ Sbjct: 1 MNNIASATLPASVKRPGYDRRALQTRIVHFGFGAFHRAHQALLTDRVLNQNGGDWGICEI 60 Query: 59 NLMPGNDRVLIENLKKQQLLYTVAEKGAESTELKIIGSMKEALHPEIDGCEGILNAMARP 118 +L G++ L+ L+ Q LYTV EKGAE + IIG++ E L+ ++DG E I+ P Sbjct: 61 SLFSGDE--LMSALRAQDHLYTVLEKGAEGNQPIIIGAVNECLNAKLDGMEAIIEKFCEP 118 Query: 119 QTAIVSLTVTEKGYCADAASGQLDLNNPLIKHDLENPTAPKSAIGYIVEALRLRREKGLK 178 Q AIVSLT+TEKGYC D A+G LD N I HDLENP AP SA G +VEAL RR +G Sbjct: 119 QVAIVSLTITEKGYCIDPATGHLDTQNSRIAHDLENPHAPHSAPGLLVEALHRRRARGHA 178 Query: 179 AFTVMSCDNVRENGHVAKVAVLGLAQARDPQLAAWIEENVTFPCTMVDRIVPAATPETLQ 238 AFTV+SCDN+ +NGHV + AVLG+A RDP LA WI ENVTFP TMVDRIVPAATPE+LQ Sbjct: 179 AFTVLSCDNIPDNGHVVREAVLGMAHQRDPALAEWIAENVTFPGTMVDRIVPAATPESLQ 238 Query: 239 EIADQLGVYDPCAIACEPFRQWVIEDNFVNGRPDWDKVGAQFVADVVPFEMMKLRMLNGS 298 EIAD LGV DPCAI+CEPF QWVIEDNFV GRP W+ G Q V DV+P+E MKLRMLNGS Sbjct: 239 EIADTLGVADPCAISCEPFIQWVIEDNFVAGRPAWEDAGVQMVDDVLPWEQMKLRMLNGS 298 Query: 299 HSFLAYLGYLGGYETIADTVTNPAYRKAAFALMMQEQAPTLSMPEGTDLNAYATLLIERF 358 HSFLAYLGYL GY+ I+D + + +R AA LM++EQAPTL + G DL YA LI RF Sbjct: 299 HSFLAYLGYLAGYQHISDCMNDTHFRDAARQLMLREQAPTLRI-TGVDLTGYADSLIARF 357 Query: 359 SNPSLRHRTWQIAMDGSQKLPQRLLDPVRLHLQNGGSWRHLALGVAGWMRYTQGVDEQGN 418 +NPSL+HRTWQIAMDGSQKLPQR+LD VR HLQNGG W LALGVAGWMRY G+D+ G Sbjct: 358 ANPSLKHRTWQIAMDGSQKLPQRMLDSVRWHLQNGGEWSLLALGVAGWMRYVSGLDDNGQ 417 Query: 419 AIDVVDPMLAEFQKINAQYQGADRVKALLGLSGIFADDLPQNADFVGAVTAAYQQLCERG 478 IDV DP+ + + +RV ALL L +F ++LPQ+ F+ + AA+Q LC G Sbjct: 418 PIDVRDPLADKIATLVQSSSEEERVSALLTLKEVFGEELPQHPLFIHTLHAAWQSLCRLG 477 Query: 479 ARECVAAL 486 A+E VA L Sbjct: 478 AKEAVARL 485 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: 787 Number of extensions: 34 Number of successful extensions: 3 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 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