Align Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; EC 2.3.1.168; Branched-chain alpha-keto acid dehydrogenase complex component E2; BCKAD-E2; BCKADE2; Dihydrolipoamide acetyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; Dihydrolipoamide branched chain transacylase; Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (uncharacterized)
to candidate WP_011938183.1 GURA_RS06435 2-oxoglutarate dehydrogenase complex dihydrolipoyllysine-residue succinyltransferase
Query= curated2:P37942 (424 letters) >NCBI__GCF_000016745.1:WP_011938183.1 Length = 413 Score = 218 bits (556), Expect = 2e-61 Identities = 140/419 (33%), Positives = 223/419 (53%), Gaps = 16/419 (3%) Query: 5 QMTMPQLGESVTEGTISKWLVAPGDKVNKYDPIAEVMTDKVNAEVPSSFTGTITELVGEE 64 ++ +P +GESV E ++KWL G+ V K +P+ E+ TDK+ E+ + G ++ V + Sbjct: 2 EIKIPAVGESVFEALVAKWLKTDGELVKKDEPLCEIETDKITLEINAEAAGVLSIRV-KA 60 Query: 65 GQTLQVGEMICKIETEGANPAEQKQEQPAASEAAENPVAKSAGAADQPNKKRYSPAVLRL 124 G+T+++G +I I+ +G A++ PV QP SPAV ++ Sbjct: 61 GETVKIGTVIGAIDEQGVPEGAVAPGVEPAAKPEFQPVTP------QPP---LSPAVRKM 111 Query: 125 AGEHGIDLDQVTGTGAGGRITRKDIQRL-IETGGVQEQNPEELKTAAPAPKSASKPEPKE 183 A E G+ + + G+G GGRIT D+ + I G + E+L A P + S P Sbjct: 112 AQEKGLKPETILGSGKGGRITVDDLLKAGIGDLGTGIGDREKLPMAGPVVEQPSLFGPAA 171 Query: 184 ETSYPASAAGDKEI---PVTGVRKAIASNMKRSKTEIPHAWTMMEVDVTNMVAYRNSIKD 240 E P A + I P+T +RK IA + + + T E D+ ++A R + + Sbjct: 172 EP-LPTQAGEEGRITRKPMTPIRKRIAERLLAVRQQTAMLTTFNEADMGRIIALRKNHNE 230 Query: 241 SFKKTEGFNLTFFAFFVKAVAQALKEFPQMNSMWAGDKIIQKKDINISIAVATEDSLFVP 300 F G L F FFVKA ALK FP +N+ GD I+ + +I IA+ E L VP Sbjct: 231 RFMLRHGVALGFMPFFVKACIDALKAFPIVNARIDGDDIVYQHFYDIGIAIGGEKGLVVP 290 Query: 301 VIKNADEKTIKGIAKDITGLAKKVRDGKLTADDMQGGTFTVNNTGSFGSVQSMGIINYPQ 360 +I++AD + + I K I ++V+ +L D+ GGTFT++N G +GS+ S IIN PQ Sbjct: 291 IIRDADRRNLAEIEKAIQVYVERVKINQLNLADITGGTFTISNGGVYGSMLSTPIINPPQ 350 Query: 361 AAILQVESIVKRPVVMDNGMIAVRDMVNLCLSLDHRVLDGLVCGRFLGRVKQILESIDE 419 + +L + +I +RPV +D G + +R M+ L LS DHR++DG FL ++K+ +E +E Sbjct: 351 SGVLGMHAIQERPVALD-GKVVIRPMMYLALSYDHRIIDGREAVGFLKKIKECIEDPEE 408 Lambda K H 0.312 0.129 0.359 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: 409 Number of extensions: 32 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: 1 Length of query: 424 Length of database: 413 Length adjustment: 32 Effective length of query: 392 Effective length of database: 381 Effective search space: 149352 Effective search space used: 149352 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.9 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Apr 09 2024. 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