Align 3-methyl-2-oxobutanoate:ferredoxin oxidoreductase (EC 1.2.7.7) (characterized)
to candidate Ac3H11_1196 Indolepyruvate ferredoxin oxidoreductase, alpha and beta subunits
Query= reanno::Cup4G11:RR42_RS19540 (1197 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_1196 Length = 1191 Score = 1465 bits (3793), Expect = 0.0 Identities = 740/1207 (61%), Positives = 917/1207 (75%), Gaps = 37/1207 (3%) Query: 1 MNAPLTPPVSDAIRRALANVSLEDKYTLERGRVYISGTQALVRLPMLQRERDRAAGLNTA 60 MNAPL +++R+AL V+L+DKY+L+ GR ++SG QALVRLPMLQR+RD AGLNTA Sbjct: 1 MNAPLP----ESVRKALETVTLDDKYSLDHGRAFMSGVQALVRLPMLQRQRDAVAGLNTA 56 Query: 61 GFISGYRGSPLGALDQSLWKAKQHLAAHDIVFQAGLNEDLAATSVWGSQQVNMYPDAR-F 119 GFISGYRGSPLG DQ+LW AK+HLAA++IVFQ G+NE+L AT+VWG+QQ+++YP ++ F Sbjct: 57 GFISGYRGSPLGTYDQALWAAKKHLAANNIVFQPGVNEELGATAVWGTQQLDLYPQSKKF 116 Query: 120 EGVFGMWYGKGPGVDRTSDVFKHANSAGSSRHGGVLVLAGDDHAAKSSTLAHQSEHIFKA 179 +GVFG+WYGKGPGVDR SDVFKHAN AG+++HGGV+ +AGDDH +KSST AHQS+HIFKA Sbjct: 117 DGVFGIWYGKGPGVDRCSDVFKHANMAGTAKHGGVIAIAGDDHISKSSTAAHQSDHIFKA 176 Query: 180 CGLPVLYPSNVQEYLDYGLHAWAMSRYSGLWVSMKCVTDVVESSASVELDPHRVEIVLPQ 239 CG PV +PS+VQE LD GLHA+AMSR+SG+W MK + +VVESS+S+ +DP RV+IV+P+ Sbjct: 177 CGTPVFFPSSVQEILDMGLHAFAMSRFSGVWSGMKTIQEVVESSSSINIDPDRVKIVMPE 236 Query: 240 DFILPPGGLNIRWPDPPLEQEARLLDYKWYAGLAYVRANKIDRIEIDSPHARFGIMTGGK 299 DF++PPGGL+IRWPD PLEQEARL+DYKWYA LAY+RANK++ I+ + RFGI+ GK Sbjct: 237 DFVMPPGGLHIRWPDAPLEQEARLMDYKWYAALAYIRANKLNYNVIEGKNDRFGIIASGK 296 Query: 300 AYLDTRQALANLGLDDETCARIGIRLYKVGCVWPLEAHGARAFAEGLQEILVVEEKRQIM 359 AY DTRQAL +LGLDD+TC ++GIR++KV VWPLEA R FA+GLQEILVVEEKRQ++ Sbjct: 297 AYNDTRQALVDLGLDDDTCRQLGIRVHKVNVVWPLEATITRDFAQGLQEILVVEEKRQVI 356 Query: 360 EYALKEELYNWRDDVRPKVYGKFDEK--DNAGGEWSI--PQSNWLLPAHYELSPAIIARA 415 EY LKEELYNWR DVRP V GKFDE D GGEWS+ P NWLL A +L+PAIIA+A Sbjct: 357 EYQLKEELYNWRADVRPNVLGKFDEPEGDATGGEWSMPNPSQNWLLRAKADLTPAIIAKA 416 Query: 416 IATRLDKFELPADVRARIAARIAVIEAKEKAMAVPRV-AAERKPWFCSGCPHNTSTNVPE 474 IA RL K + +D+ AR+ +RIAVIEA E+ MA +V ER PWFCSGCPHNTST VPE Sbjct: 417 IAKRLKKLGVSSDIIARMDSRIAVIEASERGMAELKVDTGERAPWFCSGCPHNTSTRVPE 476 Query: 475 GSRALAGIGCHYMTVWM-DRSTSTFSQMGGEGVAWIGQAPFAGDKHVFANLGDGTYFHSG 533 GSRA+AGIGCHYM WM DR TSTF+QMGGEGV W+GQAPF D HVFANLGDGTYFHSG Sbjct: 477 GSRAVAGIGCHYMANWMPDRKTSTFTQMGGEGVTWVGQAPFTTDAHVFANLGDGTYFHSG 536 Query: 534 LLAIRASIAAGVNITYKILYNDAVAMTGGQPIDGK---LSVQDVANQVAAEGARKIVVVT 590 LLAIR SIAAG +ITYK+LYNDAVAMTGGQ + + SV + N + +EG K+++VT Sbjct: 537 LLAIRQSIAAGTSITYKVLYNDAVAMTGGQTVGERPEGHSVLQIMNSLKSEGVVKLIIVT 596 Query: 591 DEPEKYSAAIKLPQGVEVHHRDELDRIQRELREVPGATILIYDQTCATEKRRRRKRGTYP 650 DEP+KY + L GV VHHRDELD +QR+ RE+ G T++IYDQTCATEKRRRRKRGT Sbjct: 597 DEPQKYD-GVALAAGVTVHHRDELDTLQRQFREIKGCTVIIYDQTCATEKRRRRKRGTLA 655 Query: 651 DPAKRAFINDAVCEGCGDCSVKSNCLSVEPLETELGTKRQINQSSCNKDFSCVNGFCPSF 710 P K IND VCEGCGDCS KSNCLSVEP+ETE G KR+INQS+CNKD+SCVNGFCPSF Sbjct: 656 TPDKTVVINDLVCEGCGDCSTKSNCLSVEPVETEFGRKRRINQSTCNKDYSCVNGFCPSF 715 Query: 711 VTAEGAQVKKP--ERHGVSMDNLPALPQPALPGLEHPYGVLVTGVGGTGVVTIGGLLGMA 768 VT EG ++KKP E+ G + LP++P+P LP E +G++V GVGGTGV+TIG LLGMA Sbjct: 716 VTVEGGKLKKPKKEKKG-DLSALPSIPEPVLPVAEAAWGIVVGGVGGTGVITIGSLLGMA 774 Query: 769 AHLENKGVTVLDMAGLAQKGGAVLSHVQIAAHPDQLHATRIAMGEADLVIGCDAIVSAID 828 AHL+ KGV D GLAQKGGA SH+QIA P+ ++ T++ +ADLVIGCD+IV+A Sbjct: 775 AHLDGKGVITQDAGGLAQKGGATWSHIQIANRPEAIYTTKVDTAKADLVIGCDSIVAAHK 834 Query: 829 DVISKTQVGRTRAIVNTAQTPTAEFIKNPKWQFPGLSAEQDVRNAVGE-ACDFINASGLA 887 ++ Q GRT +NT TPTA F+ NP WQFPG + + + AVG +A +A Sbjct: 835 YTLTVMQPGRTFVALNTHSTPTAAFVTNPDWQFPGANCDSAIAAAVGAGGVGSFDAEQVA 894 Query: 888 VALIGDAIFTNPLVLGYAWQKGWLPLSLDALVRAIELNGTAVEKNKAAFDWGRHMAHDPE 947 L+GD+I+TNPL+LGYAWQKG +PL+L +L+RA+ELNG V+ NKAAF+WGR AHD Sbjct: 895 TQLLGDSIYTNPLMLGYAWQKGRVPLTLASLMRAMELNGVQVDNNKAAFEWGRRCAHD-- 952 Query: 948 HVLSLTGKLRNTAEGAEVVKLPTSSGALLEKLIAHRAEHLTAYQDAAYAQTFRDTVSRVR 1007 L+ L A+ + VK P+ L ++IA R E LT YQ+AAYA + V +V+ Sbjct: 953 --LASVQALFQAAQVIQFVKKPS-----LTEMIAKRVEFLTGYQNAAYAAEYHAFVEKVK 1005 Query: 1008 AAESAL-VGNGKPLPLTEAAARNLSKLMAYKDEYEVARLYTDPIFLDKLRNQFEGEPGRD 1066 A ES L VG L+EA AR L KLMAYKDEYEVARL+TD F DK+ N FEG D Sbjct: 1006 ATESRLDVGT----RLSEAVARYLFKLMAYKDEYEVARLHTDKAFTDKIVNMFEG----D 1057 Query: 1067 YQLNFWLAPPLMAKRDEKGHLVKRRFGPSTMKLFGVLAKLKGLRGGVFDVFGKTAERRTE 1126 Y+L LAPP+ AK+++KG LVK+ FGP FG+LAK+KGLRG DVFGKT ERR E Sbjct: 1058 YKLVHHLAPPMTAKKNDKGELVKQPFGPWMRSAFGLLAKMKGLRGTALDVFGKTEERRME 1117 Query: 1127 RALIGEYRALLEELTRGLSAANHATAITLASLPDDIRGFGHVKDDNLAKVRTRWTALLEQ 1186 RALI EYRA ++EL L+A N A A+ +A +P++IRG+GHVK+ +L R +W L+ Q Sbjct: 1118 RALIVEYRACIDELLATLNADNLALAVEIARIPEEIRGYGHVKERHLKAARPKWDGLMAQ 1177 Query: 1187 FRHPETA 1193 +R + A Sbjct: 1178 WRSGKAA 1184 Lambda K H 0.319 0.135 0.407 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: 3290 Number of extensions: 132 Number of successful extensions: 13 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: 1197 Length of database: 1191 Length adjustment: 47 Effective length of query: 1150 Effective length of database: 1144 Effective search space: 1315600 Effective search space used: 1315600 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 (21.7 bits) S2: 59 (27.3 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