Align Glucuronate isomerase (EC 5.3.1.12) (characterized)
to candidate WP_009779311.1 MED217_RS04575 glucuronate isomerase
Query= reanno::Pedo557:CA265_RS19870 (466 letters) >NCBI__GCF_000152985.1:WP_009779311.1 Length = 475 Score = 598 bits (1542), Expect = e-175 Identities = 291/463 (62%), Positives = 359/463 (77%), Gaps = 1/463 (0%) Query: 4 FLDENFLLQSKTAEKLYHNFAKSLPIIDYHNHLIPEQIANNTQFANISQVWLAGDHYKWR 63 F+ +NFLLQ+K AE+LYH +A PIIDYHNHL P +I + QF ISQVWL+GDHYKWR Sbjct: 14 FITDNFLLQNKYAEELYHKYAAPQPIIDYHNHLPPAEIVADRQFETISQVWLSGDHYKWR 73 Query: 64 AMRANGVDEKYITGVGSDYEKFEKWAETVPYTLRNPLYHWTHLELQRYFGITDLLSGKTA 123 AMR GV+E++ITG SD EKF WA+TVP+TLRNPLYHWTHLEL+RYF I +LL+ ++ Sbjct: 74 AMRTLGVNERFITGDASDEEKFLAWAKTVPHTLRNPLYHWTHLELKRYFDIDELLNEQSG 133 Query: 124 QKIFDECSAKLQTPEYSVRGLLAKMNVEAVCTTDDPLDSLNFHQQLAREGANLKMLPAFR 183 +I+ E + +LQ E S RGLL +MNVE VCTT+DPLD+L H++ + A L M AFR Sbjct: 134 PEIYKEVNRQLQLKENSCRGLLKQMNVETVCTTEDPLDTLEQHRKYDGKKAGLNMSTAFR 193 Query: 184 PDKAMNSDDIEGLNEYIDKLESVADKTISNFQDYIDALKSRHDYFAANGCSVSDHGLEQI 243 PDKA+ + EG N Y+++LE VA +I+ + D DAL+ R D+F NGC + DHGL QI Sbjct: 194 PDKAILIE-AEGFNAYLNELEDVAKISIATYTDLQDALRQRIDFFHENGCRLCDHGLNQI 252 Query: 244 YAEDYTEAEIASIFDKIRSKQHISYEENLKFKSAMLVYFAEWDHEKGWVQQYHLGALRNN 303 + +EAEI IF K R ++ +E +FK+A+L++ E HE GWVQQ+HLGALRNN Sbjct: 253 SWAEASEAEIKEIFKKRRGGADLAPQEVEQFKTAILLFLGETYHELGWVQQFHLGALRNN 312 Query: 304 NARMLRQLGPDTGWDSIGDFSQARMLSKFLNRLDNQDKLAKTIIYNLNPADNELIATMIG 363 N RML QLGPDTGWDSIGD+SQA LS FLN LD++DKL KTIIYNLNP+DNE++ATMIG Sbjct: 313 NKRMLAQLGPDTGWDSIGDYSQAEALSNFLNALDSKDKLTKTIIYNLNPSDNEVMATMIG 372 Query: 364 NFNDGSVAGKVQFGSAWWFLDQKDGMIKQLNALSNMGLVSRLVGMLTDSRSFLSFPRHEY 423 NFNDGSV GKVQ GS WWFLDQKDGM KQ+NALSNMGL+S VGMLTDSRSFLSFPRHEY Sbjct: 373 NFNDGSVKGKVQLGSGWWFLDQKDGMEKQMNALSNMGLISCFVGMLTDSRSFLSFPRHEY 432 Query: 424 FRRIVCNLFGEDIENGELPNDLEWVGKIVQDISYFNAKNYFKF 466 FRR++CNLFG++I +GELPND++ VG+ + +ISY NAK YF F Sbjct: 433 FRRVLCNLFGQEIASGELPNDMDLVGQTIANISYHNAKEYFNF 475 Lambda K H 0.319 0.135 0.410 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: 742 Number of extensions: 18 Number of successful extensions: 2 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: 466 Length of database: 475 Length adjustment: 33 Effective length of query: 433 Effective length of database: 442 Effective search space: 191386 Effective search space used: 191386 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: 51 (24.3 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