Align phosphogluconate dehydratase (EC 4.2.1.12) (characterized)
to candidate WP_011940525.1 GURA_RS18950 dihydroxy-acid dehydratase
Query= BRENDA::Q1PAG1 (608 letters) >NCBI__GCF_000016745.1:WP_011940525.1 Length = 553 Score = 200 bits (509), Expect = 1e-55 Identities = 158/515 (30%), Positives = 244/515 (47%), Gaps = 37/515 (7%) Query: 63 MNAANVAIVSSYNDMLSAHQPYEHFPEQIKKALREMGSVGQFAGGTPAMCDGVTQGEAGM 122 M+ + + +S+ D++ H I+K + G F G P +CDG++ G GM Sbjct: 29 MDKPFIGVATSFTDLIPGHVGMRDLERFIEKGIHTGGGYAFFFG-IPGVCDGISMGHKGM 87 Query: 123 ELSLPSREVIA-LSTAVALSHNMFDAALMLGICDKIVPGLMMGALRFGHLPTIFVPGGPM 181 SLP+RE+IA + +VA +H + D ++L CDKI PG++M A R +P I V GPM Sbjct: 88 HYSLPTRELIADMVESVAEAHRL-DGLVLLTNCDKITPGMLMAAARL-DIPCIVVTAGPM 145 Query: 182 PSGISN--------KEKADVRQRYAEGKATREELLESEMKSYHSPGTCTFYGTANTNQLL 233 SG + + RY G +EL E + G+C TANT +L Sbjct: 146 MSGRGEAGRKYSFVTDTFEAMARYKAGVIDEKELKVCEDNACPGMGSCQGLFTANTMAIL 205 Query: 234 MEVMGLHLPGASFVNPYTPLRDALTHEAAQQVTRLTKQSGNFTPIGEIVDERSLVNSIVA 293 E +G+ LP + L+ + + +++ L + N TP I+ + N+I Sbjct: 206 TETLGMSLPRCGTALAVSALKRRIAFASGERIVDLVR--NNVTP-RSILTRAAFENAIRV 262 Query: 294 LHATGGSTNHTLHMPAIAQAAGIQLTWQDMADLSEVVPTLSHVYPNGKADINHFQAAGGM 353 A GGS+N LH+ AIA AG++L + L++ P L+ + P G+ + AAGG+ Sbjct: 263 DLALGGSSNTVLHLLAIAHEAGVELPLETFDILAKETPQLASMNPAGEYFMEDLDAAGGV 322 Query: 354 AFLIRELLEAGLLHEDVNTVAGRGLSRYTQEPFLDNGKLVWRDGPIESLDENILRPVARA 413 A + L++ G +D TV G + I ++DE ++ P+ Sbjct: 323 AGV---LMQLGDKIKDNPTVMGMTTLQLA--------------ASIANVDEAVIHPLTDP 365 Query: 414 FSPEGGLRVMEGNLG--RGVMKVSAVALQHQIVEAPAVVFQDQQDLADAFKAGELEKDFV 471 EGG+ ++ GNL V+K S V+ A F ++ A G ++ + Sbjct: 366 VKKEGGIAILFGNLAPKGAVVKQSGVSEAMMKFIGTARCFNSEEAAMAALMDGNIKAGDL 425 Query: 472 AVMRFQGPRSN-GMPELHKMTPFLGVLQDRGFKVALVTDGRMSGASGKIPAAIHVSPEAQ 530 V+R++GP+ GM E+ T L L G VAL+TDGR SG + + P H+SPEA Sbjct: 426 VVIRYEGPKGGPGMREMLAPTAALMGL-GLGDSVALITDGRFSGGT-RGPCIGHISPEAA 483 Query: 531 VGGALARVRDGDIIRVDGVKGTLELKVDADEFAAR 565 GG +A V DGD I +D LEL VD + R Sbjct: 484 EGGPIALVEDGDRIELDIPDRRLELLVDEQTLSER 518 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: 829 Number of extensions: 48 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: 553 Length adjustment: 36 Effective length of query: 572 Effective length of database: 517 Effective search space: 295724 Effective search space used: 295724 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