Align phosphogluconate dehydratase (EC 4.2.1.12) (characterized)
to candidate WP_078427776.1 BK574_RS05060 dihydroxy-acid dehydratase
Query= BRENDA::Q1PAG1 (608 letters) >NCBI__GCF_002019605.1:WP_078427776.1 Length = 556 Score = 207 bits (526), Expect = 1e-57 Identities = 154/513 (30%), Positives = 254/513 (49%), Gaps = 35/513 (6%) Query: 64 NAANVAIVSSYNDMLSAHQPYEHFPEQIKKALREMGSVGQFAGGTPAMCDGVTQGEAGME 123 N V I S+++++ + + + K+ G F T + DG++ G G+ Sbjct: 36 NKPFVGIASTWSEVTPCNMHIDELARKAKEGTLNGGGT-PFIFNTITVSDGISMGTEGIR 94 Query: 124 LSLPSREVIALSTAVALSHNMFDAALMLGICDKIVPGLMMGALRFGHLPTIFVPGGPMPS 183 SLPSREVIA S + +D + +G CDK +PG M+ R +LP +FV GG + + Sbjct: 95 FSLPSREVIADSIETVMGAQSYDGVVAIGGCDKNMPGCMIAIGRL-NLPAVFVYGGTIRA 153 Query: 184 GISNKEKADVRQ------RYAEGKATREELLESEMKSYHSPGTCTFYGTANTNQLLMEVM 237 G + + D+ +Y G RE+L + E + G+C TANT +E M Sbjct: 154 GKVDGKDIDIVSAFEAVGKYNNGDIDREQLHKVECHACPGAGSCGGMYTANTMASAIEAM 213 Query: 238 GLHLPGASFVNPYTP--LRDALTHEAAQQVTRLTKQSGNFTPIGEIVDERSLVNSIVALH 295 G+ LPG+S T L+D + +A + V L S TP +I+ +++ N+I + Sbjct: 214 GMSLPGSSSNPAETKEKLQDCI--DAGKAVMNLL--SKGITP-KDIMTKKAFENAITVVM 268 Query: 296 ATGGSTNHTLHMPAIAQAAGIQLTWQDMADLSEVVPTLSHVYPNGKADINHFQAAGGMAF 355 A GGSTN LH+ A+A ++L D + + VP ++ + P+GK + GG+ Sbjct: 269 ALGGSTNAVLHLLALAHTIDVELELDDFERIRKKVPHIADLKPSGKYVMEDLSLIGGVPG 328 Query: 356 LIRELLEAGLLHEDVNTVAGRGLSRYTQE--PFLDNGKLVWRDGPIESLDENILRPVARA 413 +++ LL+ GLLH D TV G+ + +E P + +++ + P + L + Sbjct: 329 VMKLLLDKGLLHGDCLTVTGQTIEENLKEIVPLKEGQEIISFENP--KRETGPLVVLRGN 386 Query: 414 FSPEGGLRVMEGNLGRGVMKVSAVALQHQIVEAPAVVFQDQQDLADAFKAGELEKDFVAV 473 +PEG L M G L+ + + PA VF ++D DA ++ V V Sbjct: 387 LAPEGALAKMSG-------------LKIKEITGPARVFDTEKDATDAVLNNKINPGDVIV 433 Query: 474 MRFQGPRSN-GMPELHKMTPFLGVLQDRGFKVALVTDGRMSGASGKIPAAIHVSPEAQVG 532 +R+ GP+ GM E+ +T + V + G KV L+TDGR SG + + H+SPEAQVG Sbjct: 434 IRYVGPKGGPGMAEMLSITAIV-VGKGLGEKVGLITDGRFSGGTHGLVVG-HISPEAQVG 491 Query: 533 GALARVRDGDIIRVDGVKGTLELKVDADEFAAR 565 G + +++GD+I ++ L + V ++FA R Sbjct: 492 GPIGLIQEGDLITINSETQELTVNVSPEKFAER 524 Lambda K H 0.318 0.134 0.386 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: 860 Number of extensions: 61 Number of successful extensions: 7 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: 608 Length of database: 556 Length adjustment: 36 Effective length of query: 572 Effective length of database: 520 Effective search space: 297440 Effective search space used: 297440 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