Align Gamma-glutamyl-putrescine synthetase (EC 6.3.1.11) (characterized)
to candidate GFF1137 PGA1_c11520 gamma-glutamylputrescine synthetase PuuA
Query= reanno::BFirm:BPHYT_RS23160 (444 letters) >FitnessBrowser__Phaeo:GFF1137 Length = 452 Score = 461 bits (1186), Expect = e-134 Identities = 221/438 (50%), Positives = 290/438 (66%) Query: 7 FLKKNRVTEIEAIIPDMAGIARGKIIPRSKFESGESMRLPQAVMIQTVTGDYPEDGTLTG 66 +L+ R+ E+E II D+ GIARGK +P SKF + LP ++ QT+TGD+ E G Sbjct: 15 YLEGRRLDEVECIISDLPGIARGKAVPASKFAKQDYFHLPDSIFYQTITGDWAEAADDDG 74 Query: 67 VTDPDMVCVPDASTIRMIPWAVDPTAQVIHDCVHFDGTPVAISPRRVLRRVLELYKAKGW 126 + DM+ PD ST PW D T QVIHD D P+ SPR VL+RV++LY KGW Sbjct: 75 WIEKDMILKPDMSTATAAPWTGDWTLQVIHDAYDRDHKPIPFSPRNVLKRVVQLYHDKGW 134 Query: 127 KPVIAPELEFYLVDMNKDPDLPLQPPIGRTGRPETGRQAYSIEAVNEFDPLFEDIYEYCE 186 +PV+APE+EF+LV N DP ++P +GR+GRP RQAYS+ AV+EF P+ +DIY++ E Sbjct: 135 QPVVAPEMEFFLVARNIDPAREIEPMMGRSGRPAAARQAYSMTAVDEFGPVIDDIYDFAE 194 Query: 187 VQELEVDTLIHEVGAAQMEINFMHGDPLKLADSVFLFKRTVREAALRHKMYATFMAKPME 246 Q E+D + E GA Q+EIN HGDP+KLAD VF FKR +REAALRH +ATFMAKP+ Sbjct: 195 AQGFEIDGITQEGGAGQLEINLRHGDPVKLADEVFYFKRLIREAALRHDCFATFMAKPIA 254 Query: 247 GEPGSAMHMHQSLVDEETGHNLFTGPDGKPTSLFTSYIAGLQKYTPALMPIFAPYINSYR 306 EPGSAMH+H S++D E+G N+F+GP G T F +I GLQ + PA + + APY+NSYR Sbjct: 255 DEPGSAMHIHHSIIDMESGDNIFSGPQGGETDAFYHFIGGLQNHLPAGLAVMAPYVNSYR 314 Query: 307 RLSRFMAAPINVAWGYDNRTVGFRIPHSGPAARRIENRIPGVDCNPYLAIAATLAAGYLG 366 R + AAPIN+ W DNRT G R+P SGP ARR+ENRI G+DCNPYL IA +LA GYLG Sbjct: 315 RYVKEQAAPINLEWARDNRTTGIRVPLSGPEARRVENRIAGMDCNPYLGIALSLACGYLG 374 Query: 367 MTQKLEATEPLLSDGYELPYQLPRNLEEGLTLMGACEPIAEVLGEKFVKAYLALKETEYE 426 + + + D Y +P+ + + L L + EVLG +F + Y +K EY+ Sbjct: 375 LVNEERPRKQFKGDAYAGDGDIPQVMGQALDLFEEASALHEVLGPEFARVYSIVKRAEYD 434 Query: 427 AFFRVISSWERRHLLLHV 444 F +VIS WER HLLL+V Sbjct: 435 EFLQVISPWEREHLLLNV 452 Lambda K H 0.321 0.138 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: 632 Number of extensions: 19 Number of successful extensions: 1 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: 444 Length of database: 452 Length adjustment: 33 Effective length of query: 411 Effective length of database: 419 Effective search space: 172209 Effective search space used: 172209 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 (21.8 bits) S2: 51 (24.3 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