Align phosphogluconate dehydratase (EC 4.2.1.12) (characterized)
to candidate WP_084055683.1 B9A12_RS01020 dihydroxy-acid dehydratase
Query= BRENDA::Q1PAG1 (608 letters) >NCBI__GCF_900176285.1:WP_084055683.1 Length = 552 Score = 247 bits (631), Expect = 8e-70 Identities = 176/515 (34%), Positives = 261/515 (50%), Gaps = 46/515 (8%) Query: 68 VAIVSSYNDMLSAHQPYEHFPEQIKKALREMGSVGQFAGGTPA------MCDGVTQGEAG 121 V IV+S+N+++ H + + +K +R AGGTP +CDG+ AG Sbjct: 34 VGIVNSFNEIIPGHIHLDKIAQAVKAGVR-------MAGGTPVEFSTIGVCDGIAMNHAG 86 Query: 122 MELSLPSREVIALSTAVALSHNMFDAALMLGICDKIVPGLMMGALRFGHLPTIFVPGGPM 181 M SL SRE+IA S V + + FDA +++ CDKI+PG++M A R ++PT+ V GGPM Sbjct: 87 MRYSLASRELIADSVEVMATAHPFDALVLIPNCDKIIPGMLMAAFRL-NIPTLLVSGGPM 145 Query: 182 PSGISNKEKADVRQ------RYAEGKATREELLESEMKSYHSPGTCTFYGTANTNQLLME 235 +G + D+ + G + EEL E E + G+C TAN+ L E Sbjct: 146 LAGRVGRRPVDLISVFEGVGAHKAGTLSTEELEELEDCACPGCGSCAGMFTANSMNCLSE 205 Query: 236 VMGLHLPGASFVNPYTPLRDALTHEAAQQVTRLTKQSGNFTPIGEIVDERSLVNSIVALH 295 +GL LPG + + R L A ++ L + N P ++V + S N+I Sbjct: 206 ALGLALPGNGTIPAVSAARFRLAKTAGMKIMDLI--AANKLP-KDLVTQASFENAIAVDM 262 Query: 296 ATGGSTNHTLHMPAIAQAAGIQLTWQDMADLSEVVPTLSHVYPNGKADINHFQAAGGMAF 355 A G STN LH+PAIA AGI L +S P L + P G + AAGG+ Sbjct: 263 ALGCSTNTVLHVPAIAHEAGITLDLDLFNSMSAKTPHLCSLRPGGPHFLEDLNAAGGIQA 322 Query: 356 LIRELLEAGLLHEDVNTVAGRGLSRYTQEPFLDNGKLVWRDGPIESLDENILRPVARAFS 415 ++REL + GL+H D TV G+ + + ++++D +++RP+ + + Sbjct: 323 VMRELAKGGLIHLDAQTVTGQTVGANLER--------------VKAVDHDVIRPLDKPYH 368 Query: 416 PEGGLRVMEGNLG--RGVMKVSAVALQHQIVEAPAVVFQDQQDLADAFKAGELEKDFVAV 473 EGG+ ++ GNL V+K SAVA + A VF+ + + A A G++ V V Sbjct: 369 QEGGIAILYGNLAPQGAVVKQSAVAHEMMQRTGRARVFESENEAASAILIGQIRPGDVVV 428 Query: 474 MRFQGPRSNGMPELHKMTPFLGVLQDRGF--KVALVTDGRMSGASGKIPAAI-HVSPEAQ 530 +R++GP+ G P + +M + RG VAL+TDGR SG G AAI H+SPEA Sbjct: 429 IRYEGPK--GGPGMQEMLTPTAAIVGRGLDKDVALITDGRFSG--GTQGAAIGHISPEAA 484 Query: 531 VGGALARVRDGDIIRVDGVKGTLELKVDADEFAAR 565 GG +A V +GD I +D LELKVD AR Sbjct: 485 AGGPIALVEEGDEIVIDIPGKKLELKVDEATLEAR 519 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: 919 Number of extensions: 42 Number of successful extensions: 8 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: 552 Length adjustment: 36 Effective length of query: 572 Effective length of database: 516 Effective search space: 295152 Effective search space used: 295152 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