Align L-arabonate dehydratase (EC 4.2.1.25) (characterized)
to candidate WP_110805670.1 C8J30_RS09805 phosphogluconate dehydratase
Query= reanno::WCS417:GFF2156 (578 letters) >NCBI__GCF_003217355.1:WP_110805670.1 Length = 606 Score = 187 bits (475), Expect = 1e-51 Identities = 154/505 (30%), Positives = 236/505 (46%), Gaps = 45/505 (8%) Query: 42 PIIGICNTWSELTPCNAHFRQIAEHVKRGVIE-------AGGFPVEFPVFSNGESNLRPT 94 P IGI ++++ +A + +K + AGG P + G + + Sbjct: 72 PNIGIVTAYNDMLSAHAPYADYPAQIKAALRAIGATAQVAGGVPAMCDGVTQGRAGME-L 130 Query: 95 AMLTRNLASMDVEEAIRGNPIDGVVLLTGCDKTTPALLMGAASCD-VPAIVVTGGPMLNG 153 ++ +R++ ++ A+ + D + L CDK P L+M AA+ +PAI + GPM G Sbjct: 131 SLFSRDVIALAAGVALSHDTFDAAIFLGVCDKIVPGLVMAAATFGHLPAIFLPAGPMTAG 190 Query: 154 KHKGQDIGSGTVVWQLSEQVKAGTITLDDFLAAEGGMSRSAGTCNTMGTASTMACMAEAL 213 + ++ +Q G + D +AAE GTC GTA+T + E + Sbjct: 191 LPNDEKA-------KVRQQFATGEVGRDKLMAAEMASYHGPGTCTFYGTANTNQMLMEVM 243 Query: 214 GTSLPH----NAAIPAVDARRYVLAHMSGMRAVEMVRED-LKLSKILTKEAFENAIRVNA 268 G LP N P DA AH + A+ + E+ L + +L + AF N + Sbjct: 244 GLHLPGASFVNPHTPLRDALTVAGAHR--VAAITALGENALPVGHLLDERAFVNGLVGLM 301 Query: 269 AIGGSTNAVIHLKAIAGRIGVELDLDDWTRIGRGMPTIVDLQPSGRFLMEEFYYAGGLPA 328 A GGSTN V+HL A+A G+ELDL+D+ I +P + + P+G + F+ AGGL Sbjct: 302 ATGGSTNLVLHLPAMARAAGIELDLEDFDDISATVPLMAKVYPNGLADVNAFHAAGGLQF 361 Query: 329 VLRRLGEANLIPHPNALTVNGKSLGENTQDSPIYG-------------QDEVIRTLDNPI 375 ++R L A L+ H + TV G L TQD+ + D ++R P Sbjct: 362 LIRHLLRAGLL-HADVNTVAGPGLARYTQDAKLIEGRLTWVEGPEDSLNDRILRPAATPF 420 Query: 376 RADGGICVLRGNLAPLGAVLKPSAASPALMQHRGRAVVFENFDMYKARINDPELDVDANS 435 A GG+ L GNL V+K SA +P A VFE+ D K E D + Sbjct: 421 AATGGLKHLAGNLG--RGVIKVSAVAPDRHVIEAPARVFESQDAVKDAFKRGEFTRD--T 476 Query: 436 ILVMKNCGPKGYPGMAEVGNMGLPAKLLAQGVTDMVRISDARMSGTAYGTV--VLHVAPE 493 ++V++ GP+ GM E+ ++ +L + ++D RMSG A G V +HV+PE Sbjct: 477 VVVVRFQGPQA-NGMPELHSLTPTLSVLQDRGLRVALVTDGRMSG-ASGKVPAAIHVSPE 534 Query: 494 AAAGGPLATVKEGDWIELDCANGRL 518 AA GGPLA + +GD I LD G L Sbjct: 535 AACGGPLARLLDGDLIRLDADTGTL 559 Lambda K H 0.319 0.136 0.413 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: 927 Number of extensions: 51 Number of successful extensions: 5 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: 578 Length of database: 606 Length adjustment: 37 Effective length of query: 541 Effective length of database: 569 Effective search space: 307829 Effective search space used: 307829 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: 53 (25.0 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