Align Putrescine oxidase; EC 1.4.3.10 (uncharacterized)
to candidate WP_110207836.1 DNK54_RS15250 NAD(P)-binding protein
Query= curated2:P40974 (478 letters) >NCBI__GCF_003194585.1:WP_110207836.1 Length = 432 Score = 151 bits (382), Expect = 4e-41 Identities = 143/460 (31%), Positives = 207/460 (45%), Gaps = 47/460 (10%) Query: 17 VVVVGAGPAGLMAARTLVAAGRTVAVLEARDRVGGRTWSKT-VDGAFLEIGGQWISPDQT 75 VVVVGAG +GL+AAR LV+AG V V EA DRVGGRT ++T V G+ L++GG WI D Sbjct: 6 VVVVGAGLSGLVAARELVSAGVDVVVAEAADRVGGRTLAETSVLGSRLDLGGTWIGHDHH 65 Query: 76 ELLALVDELGLETYQRYREGESVYLAPDGTRHT--YTGSMFPAGESTIVEMEKLVALLDG 133 + L ELG + + ++ L DG R T + PAG + +ALL Sbjct: 66 RVTELAAELGATVFPMHTG--ALPLVTDGARRTTPLVRAGLPAGAA--------LALL-A 114 Query: 134 LVAEIGATEPWAHPAARELDTISFHHWLRQHSDDEAACSNIGIFVAGGMLTKPAHAFSVL 193 L A + W ++ WL + +A + + T P + Sbjct: 115 LAARRESRATW--------QDLTVASWLGR-VPGRSARRLLEVLTQVSWTTDPDRLSART 165 Query: 194 QAVLMAASAGSFSNLVDEDFILDRRVVGGMQSVSETMAAELGEDVVFLDTPVRTIRWAGD 253 L++ G + L D V G+ +++E +A ELGE V R +R A + Sbjct: 166 MIDLISRQGGLRTMLSTRGGAQDSLVAEGVGTLAERIADELGERVRLAHRVTRIVR-APE 224 Query: 254 GGTYAEHVPGTPVTVWSDRLTVRAKDVVVAVPPNLYSRISFEPPLPRLQHQMHQHQSLGL 313 G +T+ ++ +RA V+V VPP + +RI +PPLP + + Q LG Sbjct: 225 G-----------ITLETEGGGLRAARVIVTVPPPVAARIVHDPPLPPRRAALEQGTYLGT 273 Query: 314 VIKVHAVYETPFWRDKG-----LSGTGFGAHELSQEVYDNTNHGDPRGTLVGFVSDERAD 368 V K AVYE PFWR++ L G GA V+D + G P G L A Sbjct: 274 VHKAIAVYERPFWRERRGGELLLLGRPGGA------VFDTSPPGGP-GHLTLLFGGAEAR 326 Query: 369 ELFGLPAEERRRLILESLSHYLGEEALHPVVYYESDFGSEEWTRGAYAASYDLGGLHRYG 428 L L RR +L++L +LG E ++E + +E+ G Y G Sbjct: 327 ALDALEGGVRRTRVLDALEPHLGSEVRRYAGWHEKSWHLDEYAGGGYVVLPAPGATDGRY 386 Query: 429 AHQRTPVGPIRWACSDLAAEGYQHVDGALRQGRLAAAEVL 468 PV I WA ++ A + ++DGA+ GR AA VL Sbjct: 387 DLASEPVDGIHWAGAETAVDHPGYLDGAIESGRRAARTVL 426 Score = 24.6 bits (52), Expect = 0.007 Identities = 12/28 (42%), Positives = 19/28 (67%) Query: 8 GSETAIERDVVVVGAGPAGLMAARTLVA 35 G+ETA++ + GA +G AART++A Sbjct: 400 GAETAVDHPGYLDGAIESGRRAARTVLA 427 Lambda K H 0.318 0.135 0.406 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: 696 Number of extensions: 52 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 478 Length of database: 432 Length adjustment: 33 Effective length of query: 445 Effective length of database: 399 Effective search space: 177555 Effective search space used: 177555 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 51 (24.3 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