Align 3-hydroxybenzoate--CoA/4-hydroxybenzoate--CoA ligase; 3-hydroxybenzoyl-CoA synthetase; EC 6.2.1.27; EC 6.2.1.37 (characterized)
to candidate WP_045584537.1 AL072_RS19855 AMP-binding protein
Query= SwissProt::Q9AJS8 (523 letters) >NCBI__GCF_001305595.1:WP_045584537.1 Length = 538 Score = 189 bits (479), Expect = 3e-52 Identities = 146/487 (29%), Positives = 219/487 (44%), Gaps = 17/487 (3%) Query: 41 YRELDAATNRHGNALRAHGVGKGDRVLFLMDDSPELVAAYLGTLRIGAVAVALNVRLAPR 100 + ++ A +NR NAL A GV +GDRV L+ +PE +++ ++G VAV L Sbjct: 57 FADIRALSNRFANALDAQGVVRGDRVGILLPQAPETAVSHVAVYKLGGVAVPLFSLFGVE 116 Query: 101 DVLYVIQDSACRLLYIDAEFLHLYQQIAGELEQPPQVVVRGDEAPAPAIIAFKHFLDGQA 160 + Y + + R + DA QI L P V + P + + D + Sbjct: 117 ALEYRLANCGARAVVTDAAGAAKIAQIRDRL--PELRAVFRIDGSGPGCLDWHGLCDAAS 174 Query: 161 ATLESVQVAPDDVAYWLYSSGTTGRPKAVMHAHRSVL---IADRLEREYFGIKPGDRVFT 217 PDD A +Y+SGTTG+PK +HAHR +L + + F +PGDR++T Sbjct: 175 DDFTPADTGPDDPALIIYTSGTTGQPKGALHAHRVLLGHLPGVEMSHDLFP-QPGDRIWT 233 Query: 218 TSKMFFGWSLGHSLMGGLQCGATVIVAPGWP-DAERVMATAARHRPTILFSTPV---MYR 273 + + L L+ G TV+ DAE A A + F P M R Sbjct: 234 PADWAWIGGLLDVLLPAWHHGVTVVSHRFEKFDAEAAFALLAEFQVRNAFLPPTALKMMR 293 Query: 274 NLLREGAGESAAMRDIRHFVSAGEKLPENIGQQWLDTFGIPITEGIGASE-TVFLFLCAR 332 + GA + AMR + S GE L + TFG+ I E G +E + + A Sbjct: 294 AVPDPGARHAIAMRSV---ASGGETLGAGLLDWGRQTFGVTINEFYGQTECNMIVSSAAT 350 Query: 333 PDAYRIGSCGKRVPWAEVRLLDELGNEITTPDTPGLIAIRMAS--QFVGYWKLPETTEKA 390 + G G+ VP +V ++D GN + P GLIA+ F+GYW P+ T Sbjct: 351 LMQPKPGIMGRPVPGHDVAVIDGDGNRLP-PGQIGLIAVHRPDPVMFLGYWNNPDATAAK 409 Query: 391 LRDGWYYPGDMFSFDADGFWYHNGRADDMLKISGQWVSPGEIESCASAVPGIAEAVVVAV 450 W GD D DG+ GR DD++ +G + PGEIE C P I A VV V Sbjct: 410 FIGNWLVTGDQGELDQDGYIRFVGRDDDVITSAGYRIGPGEIEDCLIGHPAIRMAAVVGV 469 Query: 451 PNDDGLTRLTLFIVPEDPSASQQKLSEAWMTTLRGTLSIYKCPRTIQFLEELPRTATGKV 510 P+ + F+V ++ L + ++ L+ ++ PR I+F+E LP T TGK+ Sbjct: 470 PDPLRTEIVKAFVVLQEDVVPDDALVASIQQHVKTKLAAHEYPRAIEFVESLPMTTTGKI 529 Query: 511 QKYRLRD 517 + LR+ Sbjct: 530 IRRELRN 536 Lambda K H 0.321 0.137 0.417 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: 837 Number of extensions: 50 Number of successful extensions: 4 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: 523 Length of database: 538 Length adjustment: 35 Effective length of query: 488 Effective length of database: 503 Effective search space: 245464 Effective search space used: 245464 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: 52 (24.6 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