Align gamma-glutamylputrescine oxidase (EC 1.4.3.-) (characterized)
to candidate Pf1N1B4_2141 Gamma-glutamyl-putrescine oxidase (EC1.4.3.-)
Query= reanno::pseudo5_N2C3_1:AO356_21495 (427 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2141 Length = 437 Score = 379 bits (973), Expect = e-109 Identities = 198/419 (47%), Positives = 266/419 (63%), Gaps = 4/419 (0%) Query: 9 SYYAASANPVPPRPALQDDVETDVCVIGAGYTGLSSALFLLENGFKVTVLEAAKVGFGAS 68 SYYAAS+ P P L ++ DVCV+G G++GL++AL L E GF V +LEA K+G+GAS Sbjct: 17 SYYAASSLPQPDLAVLTGELVADVCVVGGGFSGLNTALELAERGFSVVLLEAHKIGWGAS 76 Query: 69 GRNGGQIVNSYSRDIDVIERSVGPQQAQLLGNMAFEGGRIIRERVAKYQIQCDLKDGGVF 128 GRNGGQ++ +D +G + + M E I+R+R+ ++QI CDL G Sbjct: 77 GRNGGQLIRGVGHGLDQFANVIGADGVRQMKLMGLEAVEIVRQRIERFQIPCDLTWGYCD 136 Query: 129 AALTAKQM-GHLESQKRLWERFGHTQLELLDQRRIREVVACEEYVGGMLDMSGGHIHPLN 187 A A+ + G E L + LL + VV + YVGG++DM GH+HPLN Sbjct: 137 LANKAQDLEGFAEDAIELHSLGYRYETRLLQAHEMHSVVGSDRYVGGLIDMGSGHLHPLN 196 Query: 188 LALGEAAAVESLGGVIYEQSPAVRIERGASPVVHTPQGKVRAKFIIVAGNAYLGNLVPEL 247 LALGEAAA LG ++E+S RI+ G VHT QG VRAK +++ NAYL +L P+L Sbjct: 197 LALGEAAAAGQLGVKLFERSAVTRIDYGPEVKVHTAQGTVRAKTLVLGCNAYLNDLNPQL 256 Query: 248 AAKSMPCGTQVIATEPLGDELAHSLLPQDYCVEDCNYLLDYYRLTGDKRLIFGGGVVYGA 307 K +P G+ +IATEPL +E AH+LLPQ+ V D LDYYRL+ D+RL+FGG Y Sbjct: 257 GGKVLPAGSYIIATEPLSEEQAHALLPQNMAVCDQRVALDYYRLSADRRLLFGGACHYSG 316 Query: 308 RDPANIEAIIRPKMLKAFPQLKDVKIDYAWTGNFLLTLSRLPQVGRLGD--NIYYSQGCS 365 RDP +I A +RPKML FPQL VKIDY W G + +RLPQ+GRL + N+YY+Q S Sbjct: 317 RDPKDIAAYMRPKMLAVFPQLAGVKIDYQWGGMIGIGANRLPQIGRLKEQPNVYYAQAYS 376 Query: 366 GHGVTYTHLAGKVLAEALRG-QAERFDAFADLPHYPFPGGQLLRTPFAAMGAWYYGLRD 423 GHGV THLAGK+LAEA+ G Q+ FD FA +PH FPGG+ LR+P A+G ++ +++ Sbjct: 377 GHGVNATHLAGKLLAEAISGQQSGGFDLFAKVPHITFPGGRHLRSPLLALGMLWHRMKE 435 Lambda K H 0.320 0.139 0.421 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: 614 Number of extensions: 35 Number of successful extensions: 4 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: 427 Length of database: 437 Length adjustment: 32 Effective length of query: 395 Effective length of database: 405 Effective search space: 159975 Effective search space used: 159975 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