Align 3-methyl-2-oxobutanoate:ferredoxin oxidoreductase (EC 1.2.7.7) (characterized)
to candidate Ac3H11_2707 Indolepyruvate ferredoxin oxidoreductase, alpha and beta subunits
Query= reanno::Cup4G11:RR42_RS19540 (1197 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_2707 Length = 1161 Score = 1265 bits (3273), Expect = 0.0 Identities = 657/1174 (55%), Positives = 825/1174 (70%), Gaps = 30/1174 (2%) Query: 20 VSLEDKYTLERGRVYISGTQALVRLPMLQRERDRAAGLNTAGFISGYRGSPLGALDQSLW 79 VSL DKY L GRVY++GTQALVRL + Q+ RD AAGLNT GF+SGYRGSPLGA+DQ LW Sbjct: 5 VSLADKYELPAGRVYMNGTQALVRLLLAQKARDEAAGLNTEGFVSGYRGSPLGAVDQELW 64 Query: 80 KAKQHLAAHDIVFQAGLNEDLAATSVWGSQQVNMYPDARFEGVFGMWYGKGPGVDRTSDV 139 K + L H + FQ GLNE+LAATSVWG+Q V++ P AR +GVF +WYGKGPGVDR+ DV Sbjct: 65 KNRALLDKHKVRFQPGLNEELAATSVWGTQMVSLDPKARVDGVFALWYGKGPGVDRSGDV 124 Query: 140 FKHANSAGSSRHGGVLVLAGDDHAAKSSTLAHQSEHIFKACGLPVLYPSNVQEYLDYGLH 199 FKH N AG + HGGVL++AGDDHA KSS+L HQSEH F A +PVL+PS V E++++GLH Sbjct: 125 FKHGNIAGGAPHGGVLLVAGDDHACKSSSLPHQSEHAFIAAMIPVLHPSGVNEFIEFGLH 184 Query: 200 AWAMSRYSGLWVSMKCVTDVVESSASVELDPHRVEIVLPQDFILPPGGLNIRWPDPPLEQ 259 +AMSRYSG WV K ++D VESS+S ++DP VEI +PQ + +P G +IRWPDPPLEQ Sbjct: 185 GYAMSRYSGCWVGFKVISDTVESSSSFDIDPMSVEIKIPQSYPVPADGFSIRWPDPPLEQ 244 Query: 260 EARLLDYKWYAGLAYVRANKIDRIEIDSPHARFGIMTGGKAYLDTRQALANLGLDDETCA 319 E RL + YA L YVR NK++R + P AR GI T GK+YLD R+AL+ LGLD+ Sbjct: 245 ENRLQRERLYALLEYVRLNKLNRQDWAVPDARLGICTTGKSYLDVREALSLLGLDEAAAQ 304 Query: 320 RIGIRLYKVGCVWPLEAHGARAFAEGLQEILVVEEKRQIMEYALKEELYNWRDDVRPKVY 379 +G+RL K+G VWPLE FA+GL EILVVEEKRQ++EY +KE LYN + RP+V Sbjct: 305 ALGVRLLKIGVVWPLEPTCVVEFAQGLDEILVVEEKRQVLEYQIKEHLYN--EPHRPRVV 362 Query: 380 GKFDEKDNAGGEW-SIPQSNWLLPAHYELSPAIIARAIATRLDKF----ELPADVRARIA 434 GK+DE GEW +P S LL + EL+PA IA IA RL K LP VR + Sbjct: 363 GKYDE----SGEWVQVPSSGILLSPNGELTPAGIADVIAARLVKVYGQGVLPESVRVWLE 418 Query: 435 ARIAVIEAKEKAMAVPRVAAERKPWFCSGCPHNTSTNVPEGSRALAGIGCHYMTVWMDRS 494 + V VP +R P+FCSGCPHNTST VPEGSRALAGIGCHYM++WMDR Sbjct: 419 RQAVVATRSPSDAPVP----QRLPYFCSGCPHNTSTQVPEGSRALAGIGCHYMSMWMDRR 474 Query: 495 TSTFSQMGGEGVAWIGQAPFAGDKHVFANLGDGTYFHSGLLAIRASIAAGVNITYKILYN 554 T TFSQMGGEGV WIGQAP+ HVFANLGDGTY HSG LAIRA++AAGVNITYK+L N Sbjct: 475 TETFSQMGGEGVPWIGQAPYTDTPHVFANLGDGTYMHSGSLAIRAAVAAGVNITYKLLVN 534 Query: 555 DAVAMTGGQPIDGKLSVQDVANQVAAEGARKIVVVTDEPEKYSAAIKLPQGVEVHHRDEL 614 DAVAMTGGQP++G SV + Q+AAEG +++ +V+DEPE + A P+ V+V HRD + Sbjct: 535 DAVAMTGGQPVEGAPSVPQLLRQLAAEGVKELHLVSDEPEAFQALDDFPKDVKVSHRDGM 594 Query: 615 DRIQRELREVPGATILIYDQTCATEKRRRRKRGTYPDPAKRAFINDAVCEGCGDCSVKSN 674 D +QR LR+V G ++++Y QTCA EKRRRRK+ T DPA+R IN+AVCEGCGDC V+SN Sbjct: 595 DALQRALRDVKGVSVIVYAQTCAAEKRRRRKKKTLADPARRVVINEAVCEGCGDCGVQSN 654 Query: 675 CLSVEPLETELGTKRQINQSSCNKDFSCVNGFCPSFVTAEGAQVKKPERHGVSMDNLPAL 734 C+S+ PLET LG KRQI+QS CNKDFSCV GFCPSFV +GA+++KP+R V+ + Sbjct: 655 CVSILPLETPLGRKRQIDQSGCNKDFSCVRGFCPSFVVLDGAELRKPQRDRVAPPT--GM 712 Query: 735 PQPALPGLEHPYGVLVTGVGGTGVVTIGGLLGMAAHLENKGVTVLDMAGLAQKGGAVLSH 794 +P LP L P+ +LV GVGGTGVVTIG L+GMAAHLE KGV VLDMAGLAQKGGAV+SH Sbjct: 713 ARPELPVLARPWNILVAGVGGTGVVTIGALMGMAAHLEGKGVLVLDMAGLAQKGGAVMSH 772 Query: 795 VQIAAHPDQLHATRIAMGEADLVIGCDAIVSAIDDVISKTQVGRTRAIVNTAQTPTAEFI 854 V++AA P QLHA R+A G+AD+V+GCD +V+A D ++ GRTRA++NT PT F Sbjct: 773 VRLAADPVQLHAARVARGQADVVLGCDLMVAAAGDALASMASGRTRAVLNTDVAPTGSFT 832 Query: 855 KNPKWQFPGLSAEQDVRNAVGEACDFINASGLAVALIGDAIFTNPLVLGYAWQKGWLPLS 914 ++P WQ + + V +A + + + AS LAVAL+GDA+ TN +LG+AWQKGW+PL Sbjct: 833 RDPDWQASPDAMLERVGSAAAQV-ESLEASRLAVALMGDAVATNVFLLGFAWQKGWVPLQ 891 Query: 915 LDALVRAIELNGTAVEKNKAAFDWGRHMAHDPEHVLSLTGKLRNTAEGAEVVKLPTSSGA 974 D+L+RAIELNG AV N+AAF WGR A DP V G E V L S A Sbjct: 892 EDSLLRAIELNGAAVGMNRAAFAWGRQAALDPAAVRRAAG-----LPSDEKVMLMPSRTA 946 Query: 975 LLEKLIAHRAEHLTAYQDAAYAQTFRDTVSRVRAAESALVGNGKPLPLTEAAARNLSKLM 1034 L ++A R E L YQ+A YAQ + V RV E A VG + L A +L KLM Sbjct: 947 SLASILADRTERLADYQNARYAQHYAAVVRRVSDVEKARVGGER---LAREVAMSLYKLM 1003 Query: 1035 AYKDEYEVARLYTDPIFLDKLRNQFEGEPGRDYQLNFWLAPPLMAKRDEKGHLVKRRFGP 1094 AYKDEYEVARL+T FL +L+ +FEG D+ ++++LAPPL+A+RD +G VK+R+G Sbjct: 1004 AYKDEYEVARLHTSSDFLARLQERFEG----DFTVSYYLAPPLLARRDAQGRPVKQRYGA 1059 Query: 1095 STMKLFGVLAKLKGLRGGVFDVFGKTAERRTERALIGEYRALLEELTRGLSAANHATAIT 1154 F +LA+L+ LRG VFD FG T ERR ERA I E+ AL+E+L + L++ N A+ Sbjct: 1060 WVQTAFRLLARLRFLRGTVFDPFGWTRERREERAAIDEFEALVEDLLKDLNSNNFNEALA 1119 Query: 1155 LASLPDDIRGFGHVKDDNLAKVRTRWTALLEQFR 1188 LA LP +RG+GHVK + + LL ++R Sbjct: 1120 LARLPQQVRGYGHVKAREHEVAQKKALELLARWR 1153 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: 3279 Number of extensions: 141 Number of successful extensions: 9 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: 1161 Length adjustment: 47 Effective length of query: 1150 Effective length of database: 1114 Effective search space: 1281100 Effective search space used: 1281100 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: 58 (26.9 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:
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