Align 3-methyl-2-oxobutanoate:ferredoxin oxidoreductase (EC 1.2.7.7) (characterized)
to candidate WP_050464564.1 AKL27_RS19660 indolepyruvate ferredoxin oxidoreductase
Query= reanno::Cup4G11:RR42_RS19540 (1197 letters) >NCBI__GCF_001189915.1:WP_050464564.1 Length = 1204 Score = 1494 bits (3869), Expect = 0.0 Identities = 760/1211 (62%), Positives = 908/1211 (74%), Gaps = 33/1211 (2%) Query: 1 MNAPLTPPVSDAIRRALANVSLEDKYTLERGRVYISGTQALVRLPMLQRERDRAAGLNTA 60 MNAPL + R L ++SL+DKYTLERG V+++G QALVRLPMLQR+ D AGLNTA Sbjct: 1 MNAPL----NSGQRLLLDDISLDDKYTLERGHVFMTGIQALVRLPMLQRQADVRAGLNTA 56 Query: 61 GFISGYRGSPLGALDQSLWKAKQHLAAHDIVFQAGLNEDLAATSVWGSQQVNMYPDARFE 120 GF +GYRGSPLG +D + KAK++L A+ I F G+NEDLAATSVWG+QQVN++P A+++ Sbjct: 57 GFFTGYRGSPLGTVDLTAAKAKKYLEANHIKFHPGMNEDLAATSVWGTQQVNLFPGAQYD 116 Query: 121 GVFGMWYGKGPGVDRTSDVFKHANSAGSSRHGGVLVLAGDDHAAKSSTLAHQSEHIFKAC 180 GVFG+WYGKGPGVDR DVFKHAN AG+SRHGGVLV+AGDDHAAKSST AHQSEHI AC Sbjct: 117 GVFGLWYGKGPGVDRCGDVFKHANMAGTSRHGGVLVIAGDDHAAKSSTTAHQSEHILNAC 176 Query: 181 GLPVLYPSNVQEYLDYGLHAWAMSRYSGLWVSMKCVTDVVESSASVELDPHRVEIVLPQD 240 G+PVLYPS VQEYLDYGLH WAMSRY+GLWVS+KCVTD+VES SV +DP RV+IVLP+D Sbjct: 177 GIPVLYPSTVQEYLDYGLHGWAMSRYTGLWVSLKCVTDIVESGMSVNIDPDRVKIVLPED 236 Query: 241 FILPPGGLNIRWPDPPLEQEARLLDYKWYAGLAYVRANKIDRIEIDSPHARFGIMTGGKA 300 F LPPGGLNIR PD LEQE R+ YKWYA LAY R N++++I DSP AR GI+T GK+ Sbjct: 237 FQLPPGGLNIRQPDTVLEQETRMNVYKWYAALAYARVNQLNKIIWDSPRARIGIITAGKS 296 Query: 301 YLDTRQALANLGLDDETCARIGIRLYKVGCVWPLEAHGARAFAEGLQEILVVEEKRQIME 360 YLDTRQAL +LG+D+ IGIRLYK+G WPLEA G R FA+GL+EILVVEEKRQI+E Sbjct: 297 YLDTRQALEDLGIDENVARDIGIRLYKIGMTWPLEAEGVRNFAQGLEEILVVEEKRQILE 356 Query: 361 YALKEELYNWRDDVRPKVYGKFDEKDNAGGEWS-IPQ---SNWLLPAHYELSPAIIARAI 416 Y LKEELYNWRDDVRP+V GKFD+ GEWS PQ NWLLPA YEL+PA IARAI Sbjct: 357 YQLKEELYNWRDDVRPRVVGKFDDT----GEWSGSPQQGHGNWLLPATYELNPAQIARAI 412 Query: 417 ATRLDKFELPADVRARIAARIAVIEAKEKAMAVPRVA---AERKPWFCSGCPHNTSTNVP 473 ATR+ K+ V R+ RIA +EAKE A+ V A +R P FCSGCPHNTST +P Sbjct: 413 ATRISKYFAGHPVEQRVKVRIAYLEAKEGALNVSTKADPTKDRIPHFCSGCPHNTSTRLP 472 Query: 474 EGSRALAGIGCHYMTVWMDRSTSTFSQMGGEGVAWIGQAPFAGDKHVFANLGDGTYFHSG 533 EGSR LAGIGCHYM WMDR +S F+ MGGEGV W+GQAPF +KHVFANLGDGTYFHSG Sbjct: 473 EGSRGLAGIGCHYMVTWMDRESSLFTHMGGEGVTWVGQAPFTSEKHVFANLGDGTYFHSG 532 Query: 534 LLAIRASIAAGVNITYKILYNDAVAMTGGQPIDGKLSVQDVANQVAAEGARKIVVVTDEP 593 LLA+RAS+AA VNITYKILYNDAVAMTGGQ DG L ++ Q+AAE I+VVTDEP Sbjct: 533 LLAVRASVAASVNITYKILYNDAVAMTGGQEFDGPLDPAMISRQLAAENVTPIIVVTDEP 592 Query: 594 EKYSAAIKLPQGVEVHHRDELDRIQRELREVPGATILIYDQTCATEKRRRRKRGTYPDPA 653 +KY + +GV + HR ELD +QRELRE PG + +IYDQTCA+EKRRRRKR YPDPA Sbjct: 593 DKYPSGTPWAEGVTIRHRSELDAVQRELREKPGVSAMIYDQTCASEKRRRRKRNEYPDPA 652 Query: 654 KRAFINDAVCEGCGDCSVKSNCLSVEPLETELGTKRQINQSSCNKDFSCVNGFCPSFVTA 713 KRA IN+AVCEGCGDCSV+SNCLSVEPLETE G KRQINQSSCNKD+SCVNGFCPSFVT Sbjct: 653 KRAVINEAVCEGCGDCSVQSNCLSVEPLETEFGRKRQINQSSCNKDYSCVNGFCPSFVTV 712 Query: 714 EGAQVKKPERHGVSMDN------LPALPQPALPGLEHPYGVLVTGVGGTGVVTIGGLLGM 767 EG Q+KKP+R ALPQP LP L PYG++VTG+GGTGV+TIG +L M Sbjct: 713 EGGQLKKPKRIEAPGSKPGPDAATYALPQPVLPPLTQPYGIIVTGIGGTGVITIGQILAM 772 Query: 768 AAHLENKGVTVLDMAGLAQKGGAVLSHVQIAAHPDQLHATRIAMGEADLVIGCDAIVSAI 827 AAH+E K +VLDM+GLAQKGG V+SHV+++ H D +++TR+ G ADLVIGCD IV+A Sbjct: 773 AAHVEGKACSVLDMSGLAQKGGPVMSHVRLSDHADDIYSTRVGTGAADLVIGCDVIVTAG 832 Query: 828 DDVISKTQVGRTRAIVNTAQTPTAEFIKNPKWQFPGLSAEQDVRNAVG-EACDFINASGL 886 D +S+ GRT A VN AQTPTA F++NP WQFP SA+Q ++ A G + I+A G+ Sbjct: 833 RDALSRMGEGRTHAAVNAAQTPTAAFVRNPDWQFPAASAQQSIQEACGKDRVAMIDAGGI 892 Query: 887 AVALIGDAIFTNPLVLGYAWQKGWLPLSLDALVRAIELNGTAVEKNKAAFDWGRHMAHDP 946 A AL+GDAI TN +LGYAWQ GW+PLS AL+RAIELN +V NK AF WGR AHD Sbjct: 893 AAALLGDAIATNMFMLGYAWQHGWVPLSEAALLRAIELNALSVAFNKQAFGWGRAAAHDA 952 Query: 947 EHVLSLT-GKLRNTAEGAEVV--KLPTSSGALLEKLIAHRAEHLTAYQDAAYAQTFRDTV 1003 E VL + +T A+V+ K P S LE I R E L+AYQDAAY++ ++D V Sbjct: 953 EAVLQVARSNGMSTQPQAQVIDFKHPPS----LEHQITTRGEFLSAYQDAAYSRHYQDVV 1008 Query: 1004 SRVRAAESALVGNGKPLPLTEAAARNLSKLMAYKDEYEVARLYTDPIFLDKLRNQFEGEP 1063 +RVR AE+AL GKPL LT A A+ L KLMAYKDEYEVARL+T F +K+ FEG Sbjct: 1009 ARVRTAETALGDAGKPLRLTHAVAQYLFKLMAYKDEYEVARLHTATAFRNKISAMFEG-- 1066 Query: 1064 GRDYQLNFWLAPPLMAKRDEKGHLVKRRFGPSTMKLFGVLAKLKGLRGGVFDVFGKTAER 1123 DY+L F LAPPL A+ D KG+L+K+ FG M+ FGVLAK K LRG FD FG TAER Sbjct: 1067 --DYKLKFHLAPPLFARHDAKGYLIKQEFGSWMMQAFGVLAKFKFLRGTAFDPFGHTAER 1124 Query: 1124 RTERALIGEYRALLEELTRGLSAANHATAITLASLPDDIRGFGHVKDDNLAKVRTRWTAL 1183 + ERALI +Y+ LE L L+ AN A+ +AS+P++IRG+GH+K+ +L +++ L Sbjct: 1125 KQERALIAQYQRTLEILLARLNEANLTQAVAIASIPEEIRGYGHIKERHLLAAQSKHAEL 1184 Query: 1184 LEQFRHPETAQ 1194 + F ET Q Sbjct: 1185 MRMFDAGETPQ 1195 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: 3588 Number of extensions: 141 Number of successful extensions: 6 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: 1204 Length adjustment: 47 Effective length of query: 1150 Effective length of database: 1157 Effective search space: 1330550 Effective search space used: 1330550 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 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