Align L-arabinonate dehydratase; ArDHT; D-fuconate dehydratase; Galactonate dehydratase; L-arabonate dehydratase; EC 4.2.1.25; EC 4.2.1.67; EC 4.2.1.6 (characterized)
to candidate BPHYT_RS04815 BPHYT_RS04815 dihydroxy-acid dehydratase
Query= SwissProt::B5ZZ34 (579 letters) >FitnessBrowser__BFirm:BPHYT_RS04815 Length = 557 Score = 307 bits (787), Expect = 6e-88 Identities = 201/539 (37%), Positives = 300/539 (55%), Gaps = 21/539 (3%) Query: 35 GYPHDLFDGRPVIGILNTWSDMTPCNGHLRELAEKVKAGVWEAGGFPLEVPVFSASENTF 94 GY FD +P+IGI N S +TPCN L+ LA+ A + A P + S+ Sbjct: 27 GYEKADFD-KPMIGIANGHSTITPCNAGLQRLADAAVAAIKGADANPQIFGTPTISDGMS 85 Query: 95 RPT-----AMMYRNLAALAVEEAIRGQPMDGCVLLVGCDKTTPSLLMGAASCDLPSIVVT 149 T +++ R + + +E ++GQ MDG V++ GCDK P ++G ++PSI V Sbjct: 86 MGTEGMKYSLVSREVISDCIETCVQGQWMDGVVVIGGCDKNMPGGMIGMLRTNVPSIYVY 145 Query: 150 GGPMLNGYFRGERVGSGTHLWKFSEMVKAGEMTQAEFLEAEASMSRSSGTCNTMGTASTM 209 GG + G ++G + + E AG M+Q +F E + S+G+C M TA+TM Sbjct: 146 GGTIRPGNWKGTDLTIVSSFEAVGEFT-AGRMSQEDFDGIEQNACPSTGSCGGMYTANTM 204 Query: 210 ASMAEALGMALSGNAAIPGVDSRRKVMAQLTGRRIVQMVKDDLKPSEIMTKQAFENAIRT 269 +S EALGM+L ++ + D + A + R +V+ VK DLKP +I+TK++ ENA+ Sbjct: 205 SSSFEALGMSLLYSSTMANPDQEKVDSAAESARVLVESVKKDLKPRDIVTKKSIENAVAV 264 Query: 270 NAAIGGSTNAVIHLLAIAGRVGIDLSLDDWDRCGRDVPTIVNLMPSGKYLMEEFFYAGGL 329 A GGSTNAV+H LAIA ++ S+DD++R + VP I NL PSG+++ + AGG+ Sbjct: 265 IMATGGSTNAVLHFLAIAHAAEVEWSIDDFERMRKKVPVICNLKPSGQFVATDLHKAGGI 324 Query: 330 PVVLKRLGEAGLLHKDALTVSGETVWDEVKDV---VNWNEDVILPAEKALTSSGGIVVLR 386 P V+K L +AGLLH D +T++G T+ +E+KDV ++ VI P ++AL G + +L+ Sbjct: 325 PQVMKILLDAGLLHGDCITITGRTIAEELKDVPGKPRADQQVIFPIDQALYKEGHLAILK 384 Query: 387 GNLAPKGAVLKPSAASPHLLVHKGRAVVFEDIDDYKAKINDDNLDIDENCIMVMKNCGPK 446 GNLA GAV K + ++ G A VF+D I D + + ++V++ GPK Sbjct: 385 GNLAVDGAVAKITGLKNPVIT--GPARVFDDEQSALEAILADKIVAGD--VVVLRYLGPK 440 Query: 447 GYPGMAEVGNMGLPPKVLKKGILDMV-RISDARMSGTAYGTVVLHTSPEAAVGGPLAVVK 505 G PGM E+ + ++ KG+ + V I+D R SG +G VV H +PEA VGG +A V+ Sbjct: 441 GGPGMPEM--LAPTSAIIGKGLGESVGLITDGRFSGGTWGMVVGHVAPEAFVGGTIAFVQ 498 Query: 506 NGDMIELDVPNRRLHLDISDEELARRLAEWQPNHDLPTSG----YAFLHQQHVEGADTG 560 GD I +D L L+I + EL RR A WQ T G Y L Q +GA TG Sbjct: 499 EGDSITIDAHKLLLQLNIDNAELERRRAAWQQPKPRYTRGVMAKYFALAQPANKGAITG 557 Lambda K H 0.318 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: 913 Number of extensions: 58 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 579 Length of database: 557 Length adjustment: 36 Effective length of query: 543 Effective length of database: 521 Effective search space: 282903 Effective search space used: 282903 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Apr 09 2024. 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