Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate GFF3099 HP15_3042 bifunctional N-succinyldiaminopimelate-aminotransferase/acetylornithine transaminase protein
Query= BRENDA::P42588 (459 letters) >lcl|FitnessBrowser__Marino:GFF3099 HP15_3042 bifunctional N-succinyldiaminopimelate- aminotransferase/acetylornithine transaminase protein Length = 404 Score = 186 bits (473), Expect = 9e-52 Identities = 129/389 (33%), Positives = 201/389 (51%), Gaps = 21/389 (5%) Query: 71 GSLNTLVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLA 130 G + + D +G+EFID GG + +GH +P +V A+ +Q K S + + LA Sbjct: 29 GEGSRIWDQEGREFIDLQGGIAVTCLGHSHPGLVGALHDQAEKIWHLSNVMTNEPALRLA 88 Query: 131 KTLAALTPGKLKYSFFCNSGTESVEAALKLAKAY---QSPRGKFTFIATSGAFHGKSLGA 187 KTL LT + FF NSG E+ EAA KLA+ Y + K I+ +FHG++L Sbjct: 89 KTLCDLTFAERV--FFANSGAEANEAAFKLARRYAWEHHGKEKNEIISFKNSFHGRTLFT 146 Query: 188 LSATAKSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVI 247 +S + + + F P G H F ++E+++ +++ K A+++EPIQGEGGV+ Sbjct: 147 VSVGGQPKYLEGFEPAPGGIHHAEFNDLESVKKLISKEK-----TCAIVVEPIQGEGGVM 201 Query: 248 LPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVM 307 +L +R LCDE AL++ DEVQ+G+GR+G +A + V PDIL AK LGGG Sbjct: 202 PGDQAFLQGLRDLCDENDALLVFDEVQSGVGRSGHFYAYQMYGVVPDILSSAKGLGGG-F 260 Query: 308 PIGATIATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLL 367 P+ A + T +V + L H +T+GGN LACA A ++ + + + + + D L Sbjct: 261 PVAAMLTTAKVAASL--GVGTHGSTYGGNALACAVAQRVVDTVSQPEILKGVKARSDKLR 318 Query: 368 DGFRQLAREYPDLVQEARGKGMLMAIEFVDNEIG--YNFASEMFRQRVLVAGTLNNAKTI 425 G + Y + E RG G+L+ + G +F + + V+V + A I Sbjct: 319 KGMMDIGERY-GVFTEVRGAGLLLGCVLTEKWQGKAKDFLNAGLEEGVMV--LVAGANVI 375 Query: 426 RIEPPLTLTIEQCELVI---KAARKALAA 451 R+ P L + EL + +AA K L A Sbjct: 376 RLAPSLIIPEPDIELALERFEAAVKKLTA 404 Lambda K H 0.320 0.135 0.393 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: 410 Number of extensions: 23 Number of successful extensions: 5 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: 459 Length of database: 404 Length adjustment: 32 Effective length of query: 427 Effective length of database: 372 Effective search space: 158844 Effective search space used: 158844 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