Align Anthranilate 3-monooxygenase oxygenase component; 4-hydroxyphenylacetate 3-monooxygenase oxygenase component; 4 HPA 3-hydroxylase; Anthranilate 3-hydroxylase; Anthranilate hydroxylase; EC 1.14.14.8; EC 1.14.14.9 (characterized)
to candidate BWI76_RS15105 BWI76_RS15105 4-hydroxyphenylacetate 3-monooxygenase oxygenase component
Query= SwissProt::A4IT51 (494 letters) >FitnessBrowser__Koxy:BWI76_RS15105 Length = 504 Score = 232 bits (591), Expect = 3e-65 Identities = 148/459 (32%), Positives = 235/459 (51%), Gaps = 13/459 (2%) Query: 3 MGIRTGAQYISGLKSRKPEIWLSGRRVINVCEEPVFKQPIREIARLYDMQHDPEYQDKIT 62 + + TG +++GL + EIW G +V NV P F+ IA+LYD HD +YQ +T Sbjct: 6 VSLPTGNDFLAGLNDGR-EIWAYGEKVDNVITHPAFRNSALSIAKLYDALHDEKYQAILT 64 Query: 63 HIC-TETGERVSNAFLVPKSREDLLARRALFEVWARATFGLMGRTPDFLNVVLTSLYSNA 121 C T +G F VP S +DL+ R WAR ++G +GR+PDF LT+L +N Sbjct: 65 TPCDTGSGGVTHPFFRVPHSVDDLIRDRDAIAQWARLSYGWLGRSPDFKASFLTTLGANP 124 Query: 122 SFLEKYNPQWAENIRAYYRYVRDNDLFLTHAIINPQNDRSKPSHEQQDTFTHLGVVRETP 181 E Y ++A+N R +Y+ ++ L+ HAIINP DR+ P + +D H V +E Sbjct: 125 ---EAYG-EYADNARHWYKRSQEELLYWNHAIINPPIDRNLPPDQIEDICIH--VEKECD 178 Query: 182 EGLIVRGAKMLATLAPITDEVIIYTFPGYKPGDERYAVSFAIPIDTPGLRILCREPMQDG 241 +G+IV GAK++AT + +T I + G +A+ +P++ PGL+++CR Sbjct: 179 DGVIVSGAKVVATGSALTHYNFIAHY-GLPVKKREFALVCTLPMNAPGLKLVCRPSYSLA 237 Query: 242 TRPL---FDHPLASRFEEMDALLVFNDVLVPWDRVFIYNNVEAANLLYPKTGIAQQPAHQ 298 + FD+PL+SR++E D + + + V +PW+ +FIY + A P +G + Sbjct: 238 AEKIGSPFDYPLSSRYDENDMIFILDKVKIPWENIFIYGDTAKAATFLPSSGFLHRSTFH 297 Query: 299 TGVRGLIKLQFATEVAIRLADSIGVDVYLNVQNDLGELLQSVEAIRALLHLAEHELEVLP 358 R +K+ F + I+ ++ GV + +Q +GE+L A+ Sbjct: 298 GVTRLAVKIDFICGLFIKGVEATGVADFRGIQTRVGEMLAWRNLFWAISDAMAKSPNPWH 357 Query: 359 SGEVMPGWVPLETIRGLLPKLYPRAVEVL-QIIGAGGLLMSPTGADFANPELAADMEKYY 417 +G ++P R + YPR E++ Q +G+ + ++ DFA PEL ++KY Sbjct: 358 NGALLPNLDYGLAYRWFMSLGYPRIREIIEQDLGSALIYINSHAKDFAAPELEPYLKKYM 417 Query: 418 AGRIGVGGEERVRLFKLAWDLCGEAFGQRLLQYERFYTG 456 G G+ ERV+L KL WD G F R YER YTG Sbjct: 418 RGSNGMDAVERVKLMKLIWDSVGTEFASRHELYERNYTG 456 Lambda K H 0.322 0.139 0.418 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: 559 Number of extensions: 31 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: 494 Length of database: 504 Length adjustment: 34 Effective length of query: 460 Effective length of database: 470 Effective search space: 216200 Effective search space used: 216200 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 (21.9 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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