Align Kynurenine--oxoglutarate transaminase 1; Kynurenine--oxoglutarate transaminase I; Cysteine-S-conjugate beta-lyase; Glutamine transaminase K; GTK; Glutamine--phenylpyruvate transaminase; Kynurenine aminotransferase 1; Kynurenine aminotransferase I; KATI; EC 2.6.1.7; EC 4.4.1.13; EC 2.6.1.64 (characterized)
to candidate WP_011906689.1 SARO_RS18085 aminotransferase
Query= SwissProt::Q08415 (423 letters) >NCBI__GCF_000013325.1:WP_011906689.1 Length = 393 Score = 208 bits (529), Expect = 3e-58 Identities = 134/409 (32%), Positives = 201/409 (49%), Gaps = 34/409 (8%) Query: 12 GIDQNLWVEFGKLTKEYDVVNLGQGFPDFSPPDFATQAFQQATSGNFMLNQYTRAFGYPP 71 G+ ++ L +E +NLGQGFPD +PP +A +A + +QY G P Sbjct: 14 GMPVTIFEHMSGLARELGAINLGQGFPDEAPPPALLEALSRAAAERS--HQYPPMAGIPE 71 Query: 72 LTNVLASFFGKLLGQEMDPLTNVLVTVGAYGALFTRFQALVDEGDEVIIMEPAFDCYEPM 131 L +A F+ G E+ +V+VT GA A+ A V GDEV++ PA+D Y P+ Sbjct: 72 LRRAVAGFYAWTQGLEVGA-ESVIVTSGATEAVACAILAAVAPGDEVLLFSPAYDAYAPL 130 Query: 132 TMMAGGCPVFVTLKPSPAPKGKLGASNDWQLDPAELASKFTPRTKILVLNTPNNPLGKVF 191 AGG PVFV L P W+ D A + + TPRT+ LVLN P NP G V Sbjct: 131 IRRAGGVPVFVPLSPP-----------HWRYDEAAIVAAVTPRTRALVLNDPLNPTGTVA 179 Query: 192 SRMELELVANLCQQHDVVCISDEVYQWLVYDGHQHVSIASLPGMWDRTLTIGSAGKSFSA 251 + EL ++A+LC +HD++ I DEV++ + +DG +H S+ +LPGM RT+ IGSAGK F A Sbjct: 180 ADTELAMIASLCVRHDLIAICDEVWENVRFDGRRHRSLLALPGMARRTIKIGSAGKIFGA 239 Query: 252 TGWKVGWVMGPDNIMKHLRTVHQNSIFHCPTQAQAAVAQCFEREQQHFGQPSSYFLQLPQ 311 TGWKVGW++ ++ L HQ F Q AVAQ E G + + Sbjct: 240 TGWKVGWMVAAPDMAAVLARAHQFLTFTTAPMLQWAVAQGLEDPALAAGCTARW------ 293 Query: 312 AMELNRDHMIRSLQSVGLKLWISQGSYFLIADISDFKSKMPDLPGAEDEPYDRRFAKWMI 371 R +I +L G + + ++F D++ + DR F+ + Sbjct: 294 --AETRGVLIEALGRRGFTVLDTTATWFTCIDLAASGIALD----------DRTFSDRAV 341 Query: 372 KNMGLVGIPVSTFFSRPHQKDFDHYIRFCFVKDKATLQAMDERLRKWKE 420 + G+ IP+S + + +R C K +A L +RL +W++ Sbjct: 342 REAGVASIPLSALWEGDAAP--EGIVRLCHCKPEAMLLEAMDRLVRWRD 388 Lambda K H 0.322 0.137 0.431 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: 458 Number of extensions: 23 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: 423 Length of database: 393 Length adjustment: 31 Effective length of query: 392 Effective length of database: 362 Effective search space: 141904 Effective search space used: 141904 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 (21.9 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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